Upload
others
View
6
Download
0
Embed Size (px)
Citation preview
i
THE RELATIONSHIP BETWEEN LOCATION AND SIZE OF
UTERINE FIBROID MASS AND UPPER RENAL TRACT
CHANGES USING SONOGRAPHY IN ILORIN, NIGERIA.
A DISSERTATION SUBMITTED TO THE NATIONAL POSTGRADUATE MEDICAL COLLEGE OF NIGERIA IN PART FULFILMENT FOR THE AWARD OF FELLOWSHIP OF THE MEDICAL COLLEGE IN RADIOLOGY (FMCR) NIGERIA
BY
DR HALIMAT JUMAI AKANDE MBBS (ILORIN) 1997
NOVEMBER 2005.
ii
CERTIFICATION
I certify that this work was carried out by Dr Halimat Jumai Akande of the department of
Radiology, University of Ilorin Teaching Hospital, Ilorin Nigeria under supervision of
……………………………..
PROF.D.A.NZEH
Consultant Radiologist,
Dept. of Radiology,
University of Ilorin Teaching Hospital,
Ilorin,Kwara State.
iii
TABLE OF CONTENTS
Page
Title page ----------------------------------------------------------------------- i
Certification ---------------------------------------------------------------------- ii
Table of contents------------------------------------------------------------------iii
Introduction ---------------------------------------------------------------------- 1-2
Gross Anatomy ----------------------------------------------------------------- 3-4
Ultrasonographic anatomy of the upper renal tract ------------------------ 4-7
Literature review ---------------------------------------------------------------- 8-15
Aims and objectives -------------------------------------------------------------16
Materials and method ----------------------------------------------------------- 17-22
Results ---------------------------------------------------------------------------- 23-36
Discussion ------------------------------------------------------------------------ 37-39
Limitations ----------------------------------------------------------------------- 40
Summary -------------------------------------------------------------------------- 41
References ------------------------------------------------------------------------ 42-46
1
INTRODUCTION
One of the most common human tumours and much the most frequent uterine neoplasm, is
the myoma 1 . Although arising in the muscular wall of the uterus, there is always some
admixture of fibrous tissue in these tumors, hence the term fibromyoma. Other terms in
common use include fibroid, myoma, leiomyoma 2.
The prevalence rate varies from 20 – 25 % of women depending on age, ethnicity, parity and
imaging techniques used to assess their presence 3,4. Studies have shown that it usually
occurs from age 25 years onwards 1,5-7.
Fibroids are generally said to be higher in blacks than in whites 2,8. Prospective studies show
that black women have a three-fold greater frequency of myomas and a relative risk two to
three times that in white women 9.
The precise aetiology of uterine fibroids is unknown, but occurrence mainly in the
childbearing age suggests at least a partial role for estrogen 2. Uterine fibroids are not a
clinical problem before puberty and should not grow after menopause 10. Factors such as
being parous, use of oral contraceptive and cigarette smoking have been reported to decrease
the risk of fibroids 11-13, while factors like obesity and high parity increase the risk of fibroids
13,14.
Uterine fibroids are frequently asymptomatic, but are a recognized cause of menorrhagia,
dysmenorrhea, irregular vaginal bleeding, lower abdominal mass and distension 15.
Apart from the symptoms related to the genital system, they can also give pressure effects
and cause compression or displacement of the ureters, bladder or rectum 10. The urinary
symptoms may be explained by the close relationship of the pelvic part of the ureter to the
lateral fornix of the vagina and the cervix which makes the pelvic part of the ureter
susceptible to compression by a fibroid mass 16-18 . This compression can lead to generation
of a backpressure effect manifested by the dilatation of the ureters and the pelvicalyceal
2
collecting systems from its mildest to severe forms. The upper renal tract changes associated
with uterine fibroid mass are usually chronic in nature 19.
This study is intended to make apparent the relationship between the size and location of
uterine fibroid and the upper renal tract changes as well as highlight the benefits of renal
ultrasound in these patients.
3
GROSS ANATOMY
The uterus, an important and essential female reproductive organ, is pear-shaped and lies
between the urinary bladder and the rectum. It is made up of the fundus, body and cervix and
it is about 7.5cm in length 17. The wider body narrows to become the cervical canal at the
isthmus. The internal os is at the upper end of the cervical canal and the external os at its
lower end. The fallopian tubes open into the cornua of the uterus superolaterally.
The wall of the uterus is very thick and consists of three layers: serous, muscular and
mucous 20. Any of these layers can give rise to uterine myoma.
The serous layer (perimetrium) is simply the peritoneal covering and is firmly adherent over
the fundus and most of the body. The myometrium is the muscular layer and majority of
uterine myomas arises from this later. This smooth muscle layer is made up of an outer part
which is weaker and composed of longitudinal fibres; and an inner,stronger part composed of
interlacing fibres. The mucous layer (endometrium) is soft and spongy and consists of tissue
resembling embryonic connective tissue. The surface consists of a single layer of ciliated
columnar epithelium and this characteristics makes it more likely to cause menorrhagia when
a myoma is located in this layer 7.
The anterior and posterior peritoneal reflections of the uterus form the uterovesical pouch
and the pouch of Douglas respectively. The lateral reflection forms the broad ligament
through which the ureters (pelvic portion), running posterior to the uterine artery, attain a
close lateral relation to the lateral vaginal fornix before entering the bladder. This makes the
ureters susceptible to compression by fibroid masses especially those located in the cervix
(cervical) or within the broad ligament (intra-ligamentary). The intrabdominal portion of the
ureter extending from the termination of the pelvis courses downwards and slightly medially
anterior to the psoas major muscle in the retroperitoneal space. The entire length spans a
distance of about 26-28cm with a diameter of approximately 3mm except at its areas of
constriction, these are: the junction of the pelvis and ureter; the pelvic brim and the entrance
4
into the bladder 18. The entire length of the ureters leading to the pelves and the renal
collecting systems can be dilated by backpressure effect secondary to compression of the
ureters. The kidney being an organ of excretion may lose its filtration and secretory abilities
in the event of obstruction. The kidneys are retroperitoneal in location and lie obliquely with
their upper poles more medial and posterior than the lower poles. The renal parenchyma is
composed of an outer cortex and an inner medulla. The collecting system is made up of
minor calyces combining to form two, three or more major calyces which in turn unite to
form the pelvis of the kidney. The pelvis most frequently is intrarenal but could partly or
entirely be extrarenal. The latter could be mistaken for hydronephrosis on ultrasound.
ULTRASONOGRAPHIC ANATOMY OF THE UPPER RENAL TRACT.
Ultrasound of the kidneys is done most preferrably with the patient prone or in oblique
position to allow demonstration of the entire length of the kidneys. With the liver and spleen
providing acoustic windows on the right and left respectively, the kidneys are seen to be oval
shaped on longitudinal scan and round on transverse scan. The parenchyma appears
relatively hypoechoic to that of the liver and spleen and this surrounds a dense echogenic fat
filled renal sinus.
The normal length is between 8-13cm . In the male, this averages 10.6cm on the left and
10.3cm on the right; while in the female the corresponding length is 10.2cm on the left and
9.94cm on the right respectively21. The parenchyma is composed of the centrally located
pyramids or medulla surrounded by the peripherally located cortex. The bases of the
triangular pyramids (medulla) are usually identified by bright dots denoting the arcuate
arteries and this area differentiates the cortex from the medulla on a good quality image. The
parenchyma is surrounded by the perinephric fat, which is seen as an echogenic rim. The
bright echogenic centre is largely produced by renal sinus fat with vessels and collecting
system contributing to it. The normal pelvicalyceal system is not easily seen but occasionally
5
in well-hydrated patients, it is seen as symmetrical anaechoic area occupying the centre of
the kidney (Fig.1a-c). An extrarenal pelvis, which is a normal variant may be demonstrated if
present.
The ureters, which arise from the renal pelves are difficult to demonstrate on ultrasound
when not dilated. The normal calibre is about 3mm 2. The entire length of the ureter may be
visualised in hydroureter secondary to distal compression of the ureter.22.
6
Liver
Cortex
Pyramid
Minor Calyx
Major Calyx
Pelvis
Papilla
Ureter
Fig. 1a Schematic diagram of the internal structure of the Kidney
Renal Column of cortex (of bertin)
Capsule
Cortex
Pyramids
Sinus echoes
Fig 1b Schematic diagram of the ultrasonographic appearance of the right kidney.
7
8
LITERATURE REVIEW
UTERINE FIBROIDS
Uterine myomas are benign clonal tumours that arise from the smooth-muscle cells of the
human uterus and are the most common pathological growth in the female reproductive tract.
It affects 20-25% of all women from the age of 25years onwards 1,5-7. The true clinical
prevalence may be higher with newer imaging techniques like the magnetic resonance
imaging (MRI). Careful pathological examination of surgical specimens suggests that the
prevalence is as high as 77% 23,24 and Entman in his study reported that the incidence of
fibroid had been estimated as high as 50% in autopsy series25. In the review carried out by
Aboyeji and Ijaiya 15, in Ilorin, it was found that fibroid constituted 13.4% of gynaecological
admission while 3.2%, 8.3% and 7.8% were the incidence recorded in Zaria, Ilesha and
Benin city respectively 26,27,28. These recorded incidences though low when compared to
figures from studies in Europe, may not be the actual incidence because of the low socio-
economic status in this enviroment which prevents patients from seeking medical treatment
in the hospitals. Other studies indicate a higher incidence in blacks when compared with
whites 2,24 . This claim has been disputed by Akinkugbe in Lagos, Nigeria 5.
The precise aetiology of uterine fibroid is not known. They are most often seen after
menarche and the majority atrophy after the menopause 29. Myoma has been reported in
female as young as 11yrs of age 1. Restriction mainly to the reproductive age suggests at least
a partial role for estrogen 2, but the occurrence of fibroid in just some women and not others,
since estrogen is produced in practically all women raises the possibility of genetic
predisposition 7,30. A study carried out on the heritability and risk factors of uterine fibroids
however concluded that reproductive and anthropometrical factors may have at least a large
role in pathogenesis of fibroids than genetic factors 14. Increased body mass index in obese
patients has been reported to increase the risk of uterine fibroid. This has led to the
postulation that body fat contributes to increase estrogen production via aromatization of
9
androgen31. Factors associated with reduced risk for fibroids include the use of oral
contraceptive and cigarette smoking. It has been reported that the use of oral contraceptive
for five consecutive years reduce the risk of fibroids by 17% and women who smoke 10
sticks of cigarette daily have an 18% lowered risk compared to non-smokers 13.
The pathogenesis of myoma involves the transformation of normal myocytes into abnormal
ones and their growth into clinically apparent tumour via clonal expansion 32,33. On histology,
they reveal a whorled pattern of smooth muscle and fibrous connective tissue in varying
proportions. Grossly, they are buff-colored, rounded, smooth and firm and usually lighter in
colour than the myometrium.
Uterine fibroids are usually asymptomatic.They may however present with menorrhagia and
hypermenorrhea which can lead to iron deficiency anaemia. It can also present with pain
secondary to degenerations within the tumour. The degeneration may be atrophic, hyaline,
cystic, calcific, septic, carneous(red), or myxomatous degenerations. Spontaneous abortion
and infertility are also frequent presentations by patients but the true incidence of
spontaneous abortion is unknown and the relationship with infertility remains controversial
13,20. Pressure symptoms can result from compression of surrounding structures like ureters,
bladder, rectum and blood vessels to produce ureteric obstruction with hydronephrosis, acute
urinary retention, constipation and oedema of the lower extremities respectively.
The urinary tract changes depend on the size and location of the uterine fibroid and are
reported to be commoner with anterior intramural, cervical and intraligamentary types. Also,
intraligamentary fibroids may stimulate erythropoietin production from the renal system
leading to polycythaemia 20.
The types of uterine fibroid depend on their locations as shown below in figure 2.
10
Subserosal
Submucosal
Intramural
Endometral LiningPedunculated
Cervix
Vagina
Subserosal
Submucosal
Intramural
Endometral LiningPedunculated
Cervix
Vagina
Subserosal
Submucosal
Intramural
Endometral LiningPedunculated
Cervix
Vagina
Subserosal
Submucosal
Intramural
Endometral LiningPedunculated
Cervix
Vagina
Subserosal
Submucosal
Intramural
Endometral LiningPedunculated
Cervix
Vagina
Fig. 2 Schematic Diagram showing the sites of Uterine Myomas. A, B, C are mixed types.
11
Uterine fibroids may be corporeal or cervical, the cervical constituting only a small fraction
of the total number 1. However, the close relationship of the ureters to the cervix makes the
cervical fibroids significant in terms of the possible urinary tract changes they can produce.
Depending on which layer of the uterus the corporeal fibroids arise from, they can further be
classified as subserous, interstitial (intramural) and submucous corresponding to growth just
beneath the serous coat, muscular wall and the mucosa respectively (Fig.2). Any of these
subtypes of myoma may acquire an extrauterine blood supply from omental vessels with its
pedicle becoming atrophied to form a parasitic fibroid. Intraligamentary fibroids are
subserous tumours arising laterally from within the two layers of the broad ligament. The
identification of any of these types of uterine fibroid, can readily be achieved by
ultrasonography.
Ultrasonography is cheap, readily available and relatively non-hazardous. It involves the use
of high frequency sound waves to visualise the body organs. A trans-abdominal ultrasound of
the pelvis requires a moderately full bladder to displace the small bowel into the abdominal
cavity and straighten out the body of the uterus (corpus uteri) relative to the cervix. The
distended bladder also provides an acoustic window whereby the pelvic organs can be seen.
A 3.5MHz transducer, most preferably sector is used. The ultrasound appearance of fibroid
varies considerably, but typically is seen as solid masses with a whorled stromal pattern 34.
Cystic degeneration is seen as an area of hypoechogenicity and calcifications seen as areas of
hyperechogenicity.These calcifications are most often amorphous in nature.However it has
been reported that ultrasound does not differentiate with consistent accuracy the difference
between uterine and ovarian masses moreso,if the fibroid is a subserous pedunculated type 10.
Other investigative modalities include conventional radiography, computed radiography and
magnetic resonance imaging35.
12
The presence of a fibroid mass may be suspected on a plain radiograph of an adult female
when a mass of soft tissue density with or without areas of calcification is seen. However,
plain radiography is contraindicated when there is possibility of pregnancy.
Magnetic resonance imaging (MRI) gives better visualization of individual myoma, but for
most clinical indications the extra cost is not justified. Moreover, it is yet to be readily
available in this environment.
Computed tomography (CT) will give individual characteristics of the fibroid but its use is
limited because of the high cost and the harmful effect of radiation .
Intravenous urography (IVU) is also used not in the diagnosis but in the work-up to show the
effects on the upper and lower urinary tracts. It reveals any ureteral deviation or compression
and identifies genitourinary anomaly 10. However, as in the other investigative modalities
utilizing ionizing radiation, the harmful effect of ionizing radiation is a limiting factor.
Reactions to contrast medium from the mildest to most severe types could occur. Moreover,
IVU depends on a functioning kidney, thus a compromised non-functioning kidney will not
be demonstrated. Ultrasound is usually the first radiological investigation of choice in this
situation. It is simple, non-invasive in nature and quickly ascertains presence and location
of the kidney and shows calyceal dilatation if present 19,36.
The complications of uterine fibroid include anaemia secondary to the abnormal uterine
bleeding 10, degenerative changes 2, infertility13,37, spontaneous abortions 13,37, abnormal lie
during pregnancy 1, obstruction during labour 1 and acute urinary retention secondary to
pressure effects38.
The management of uterine fibroid could be medical or surgical depending on the age, parity
and reproductive desirability of the patients. The surgical management could either be
myomectomy or hysterectomy 39.
13
PATHOPHYSIOLOGY OF OBSTRUCTION
In order to appreciate upper renal tract changes secondary to obstruction, an understanding of
the pathophysiology of obstructive uropathy is indispensable. Impedance to the flow of urine,
urinary tract dilatation, reduction in flow rate, varying intra-renal pressures and functional
impairment play sequential roles in producing these changes 19. These changes are
collectively referred to as obstructive uropathy.
Impedance to the flow of urine usually is as a result of compression of any part of the ureter
and this leads to increase in the renal pelvic pressure which normally is below 12mmHg with
mean being 6.5mmHg 40. The increased intraluminal pressure leads to more forceful
contractions of the muscles of the renal pelvis and ureter with resultant dilatation of the part
proximal to the obstruction.
In cases of chronic obstruction however, such as caused by pelvic masses like uterine fibroid,
hydrostatic pressure continues to rise despite ureteric dilatation. Energy is used preferentially
to maintain muscle tone rather than peristalsis and the ureter becomes a passive conduit 41.
There is gradual fall of pressure towards normal in addition to contributions from decrease
glomerular filtration rate and increase reabsorption of urine from the renal pelvis 42 .
Functional impairment may result following prolonged obstruction, causing hydronephrosis,
however, the function may still be preserved despite huge hydronephrosis according to
Green et al 43. On the other hand, hydronephrosis may be present without obstruction in
some patients in which there is congenital abnormal smooth muscle of the renal pelvis or
ureter causing ectasia 44.
Many investigative modalities can be used to diagnose obstructive changes.These include
intravenous urography, antegrade pyelogram, retrograde pyelogram, radionuclide studies,
perfusion pressure flow studies, cystometry, cystourethroscopy and of interest in this study
ultrasound.19.
14
The urographic studies are of greatest value in acute obstruction, permitting the site of
obstruction and anatomy of the urinary tract to be determined. The limitations however are
their invasiveness, reaction to contrast medium and radiation exposure.
Radionuclide studies are of most significance in assessing quantitatively and non-invasively
individual renal function 19. This procedure is becoming widely used in the developed
countries 45,46 .
Perfusion pressure flow study entails the percutaneous antegrade puncture of a dilated renal
pelvis or ureter and measurement of the pressure after perfusion with saline or contrast
medium. It is also invasive and reaction to contrast medium can occur. Furthermore,it gives
no information on renal function.
Ultrasound has been reported by Ellenbogen et al to be an effective screening test in patients
with obstruction 47. Ultrasound is cheap, non-invasive and non-hazardous. Ultrasound
overcomes many of the inherent limitations of excretory urography and provides an excellent
anatomic information of the renal systems with an added advantage of showing in most cases
the cause of obstruction 48. Ultrasound demonstrates dilated pelvicalyceal system as seen by
separation of the echogenic renal sinus complex. Hydronephrosis can exist in varying
degrees and duration, the residual parenchymal thickness serving as an important indicator of
severity 49.
The different grades of hydronephrosis are as follows:
Grade 0: central collecting system echoes compact and homogenous.
Grade 1: slight separation of the collecting system echoes with a central ovoid or
fusiform sonolucency.
Grade 2: further separation of collecting system echoes with a rounded sonolucency
seen centrally.
Grade 3: Major portion of the kidney replaced by a sonolucent sac.
The grades 2 and 3 are detected with 100% accuracy on ultrasound 47
15
Ultrasound, though an excellent screening modality has its own pitfalls. It could misdiagnose
a dilated renal pelvis not caused by an obstruction giving a false positive reading.It is also
operator dependent. However, these should not prevent ultrasound from being used as a
screening test in patients suspected of having features of obstruction.
16
AIMS AND OBJECTIVES
1. To determine the relationship between the size and location of the uterine fibroid mass
and the upper renal tract changes.
17
MATERIALS AND METHODS.
This study was carried out in the university of Ilorin Teaching Hospital between June 2004
and June 2005. The sample size was determined using Fisher’s formula. For population size
greater than 10,000:
n = z2 pq
d2
where: n = the desired sample size(when population is greater than 10,000)
z = standard normal deviate,usually set at 1.96
p = the proportion in the target population estimated to have a particular
characteristics.
q = 1.0 – p
d = degree of accuracy desired,usually set at 0.5 .
A total of seventy- six patients were used for the study as against One hundred and ten
patients calculated as stated above. The reason for this being that the ultrasound scan
machine at the maternity wing of the hospital broke down during the period of study leading
to reduction in the turn out of patients.
Patients clinically suspected or confirmed to have uterine fibroid referred to the radiology
department from June 2004 to June 2005 were included in this study.
Criteria for exclusion were:
1. Patients having uterine fibroid co-existing with pregnancy or other pelvic mass.
2. Patients with known renal pathology co-existing with uterine fibroid.
A concept/D Dynamic Imaging Ultrasound machine equipped with 3.5MHz and 5.0MHz
transducers was used for all the ultrasound scans.
All the patients were asked to take lots of fluid to achieve a full bladder needed for
evaluation of the pelvis organs. The uterus was scanned transabdominally in longitudinal and
tranverse planes with the patient in the supine position. The 5.0MHz transducer was used for
most patients while the 3.5MHz transducers was used for the obese patients. Localization of
18
a fibroid nodule was done by identifying any well circumscribed isoehoic or hypoehoic mass
lesion in any part of the uterine layer. Areas of cystic degeneration or calcification were
identified as hypoechoic or highly hyperechoic focus.
The location of the fibroid nodule was based on the uterine layer of origin, which are:
i) Submucus: fibroid intruding into or are contained in the endometrial cavity.
ii) Intramural/ Interstitial: fibroid located in the muscular wall.
iii) Subserous: fibroid located just below the serous layer.
iv) Mixed: combination of any of 1-3 above.
v) Cervical: fibroid located within the cervix.
For this study, the size was taken as the widest diameter of a fibroid mass. Some of the
patients for this study had more than one fibroid mass but the diameter of the largest fibroid
mass was taken to prevent any ambuiguity.
Patients were allowed to void and then placed in the prone position to assess the kidneys.
This was done for optimal visualization of the kidneys and to prevent false positive results in
assesement of calyceal dilatation. The longest distance between the upper and lower pole of
the right and left kidneys were measured to get their bipolar length (Fig. 3).
The renal parenchymal thickness assessed on longitudinal and transverse views was taken as
the distance between the echogenic edge of the central renal sinus to the echogenic renal
capsule (Figs. 4).
Degree of calyceal dilatation was graded as follows 49:
Grade 0: Central collecting system echoes compact and homogenous.
Grade 1: Slight separation of the collecting system echoes with a central ovoid or
fusiform sonolucency (Fig. 5).
Grade 2: Further separation of the collecting system echoes with a rounded
sonolucency centrally (Fig. 6).
Grade 3: Major portion of the kidney replaced by a sonolucent sac (Fig.7).
19
The right and left ureters were looked for and when visualised, the diameter of each was
taken and graded as below:
Grade 0: Non- visualised or ureter calibre less or equal to 3mm.
Grade 1: Ureter calibre between 4-6mm (Fig.7).
Grade 2: Ureter calibre between 7-9mm.
Grade 3: Ureter calibre greater than 10mm.
Data collected was collated and analysed using the EPINFO version 6.0. Data analysis was
done using descriptive analysis for mean and measure of dispersion, Chi square of
significance to compare proportions and Student’s t-test for comparism between the means of
two groups. The relationship between two variables was done by the Pearson correlation.
Sketch diagrams, histograms and pie charts used where necessary.
FIG.1 MEASUREMENT OF
RENAL LEANGH
20
Fig. 3 Longitudinal renal scan measuring the kidney bipolar lenght
Fig. 4 Longitudinal and transverse scans showing the measurement of the renal parenchyma thickness . Renal Parenchyma Thickness
Fig. 3 Longitudinal renal scan measuring the kidney bipolar lenght
Fig. 4 Longitudinal and transverse scans showing the measurement of the renal parenchyma thickness . Renal Parenchyma Thickness
Fig. 3 Longitudinal renal scan measuring the kidney bipolar lenght
Fig. 4 Longitudinal and transverse scans showing the measurement of the renal parenchyma thickness . Renal Parenchyma Thickness
Fig. 3 Longitudinal renal scan measuring the kidney bipolar lenght
Fig. 4 Longitudinal and transverse scans showing the measurement of the renal parenchyma thickness . Renal Parenchyma Thickness
Fig. 3 Longitudinal renal scan measuring the kidney bipolar lenght
Fig. 4 Longitudinal and transverse scans showing the measurement of the renal parenchyma thickness . Renal Parenchyma Thickness
21
Fig. 6 Longitudinal ultrasound scan of the kidney showing grade 2 hydrocalycosis.
Fig. 5 Longitudinal ultrasound scan of the kidney showing grade 1 hydrocalycosis.
Fig. 6 Longitudinal ultrasound scan of the kidney showing grade 2 hydrocalycosis.
Fig. 5 Longitudinal ultrasound scan of the kidney showing grade 1 hydrocalycosis.
Fig. 6 Longitudinal ultrasound scan of the kidney showing grade 2 hydrocalycosis.
Fig. 5 Longitudinal ultrasound scan of the kidney showing grade 1 hydrocalycosis.
Fig. 6 Longitudinal ultrasound scan of the kidney showing grade 2 hydrocalycosis.
Fig. 5 Longitudinal ultrasound scan of the kidney showing grade 1 hydrocalycosis.
Fig. 6 Longitudinal ultrasound scan of the kidney showing grade 2 hydrocalycosis.
Fig. 5 Longitudinal ultrasound scan of the kidney showing grade 1 hydrocalycosis.
22
Fig. 7 Longitudinal ultrasound scan of the kidney showing grade 3 hydrocalycosis and grade 2 hydroureter.Fig. 7 Longitudinal ultrasound scan of the kidney showing grade 3 hydrocalycosis and grade 2 hydroureter.Fig. 7 Longitudinal ultrasound scan of the kidney showing grade 3 hydrocalycosis and grade 2 hydroureter.Fig. 7 Longitudinal ultrasound scan of the kidney showing grade 3 hydrocalycosis and grade 2 hydroureter.Fig. 7 Longitudinal ultrasound scan of the kidney showing grade 3 hydrocalycosis and grade 2 hydroureter.
23
RESULTS
The result of this study has been analysed first, using the mean of each data for the entire
patients on one hand, and then using the mean of a data with the different fibroid locations
and their mean sizes.
A total of 76 clinically diagnosed uterine fibroid patients were recruited into the study over a
period of one year – June 2004 – June 2005.
Table 1 shows the age distribution of the patients.
The age of the patients was ranged between 19 and 70years (mean 33.8, SD+8.9 years).
Table 1: Age distribution of the patients.
Age(years)
Frequency
%
15-24
11
14.5
25-34
34
44.7
35-44
23
30.3
45-54
6
7.9
55+
2
2.6
Total
76
100.0
24
Table 2 shows the mean age by fibroid location.
The mean ages of submucus, intramural, subserous and cervical fibroid subjects were
30.4(SD+3.0), 34.4(SD+9.9), 39.4(SD+2.1) and 32.6(SD+10.4) years respectively.
Table 2: Mean age by fibroid location.
Mean Age (Years) Fibroid location
30.4 Submucous
34.4 Intramural
39.4 Subserous
32.6 Cervical
25
Table 3 and Figure 1 show the mean parity and mean parity by fibroid location respeactively.
The mean parity of the subjects was 2.18 (SD+2.40). Majority (82.9%) of the subjects had a
parity between 0-4, while 17.1% were between 5-9.
The mean parity for the submucus fibroid subjects was 1.8 (SD+2.6), 2.2(SD+2.5) for
intramural, 3.4(SD+1.6) for subserous, and 2(SD+2.0) for cervical fibroid subjects.
Table 3: Parity and mean age of the patients:
Parity
Mean age (years)
Frequency
%
0
28.4
31
40.8
1
34.8
9
11.8
2
31.8
4
5.3
3
34.4
7
9.2
4
34.3
12
15.8
5
45.0
5
6.6
6
43.2
5
6.6
7
48.0
1
1.3
9
54.0
2
2.6
Total
33.8
76
100.0
26
FIGURE 1: Pie chart showing the parity distribution of the patients.
Pie chart showing the Parity distribution of the subjects.
1
40%
2
12%
3
5%
4
9%
5
16%
6
7%
7
7%
8
1%
9
3%
KEY
1- Parity 0
2- Parity 1
3- Parity 2
4- Parity 3
5- Parity 4
6- Parity 5
7- Parity 6
8- Parity 7
9- Parity 9
27
Table 4 showed the frequency distribution of the subjects menarche age.
The mean of the menarche was 13.4 (SD+1.48) years. Majority of the subjects attained
menarche at between 12-14 years.
Table 4: The distribution of Menarche by patients.
Age of Menarche
Frequency
%
11 6
7.9
12 18
23.7
13 17
22.4
14 17
22.4
15 10
13.2
16 7
9.2
17 1
1.3
Total 76
100.0
28
The study revealed that the mean menstral flow duration was 6.9 (SD+1.6) days for
submucous fibroid, 5.1 (SD+1.8) days for the intramural fibroid, 6.4 (SD+0.6)days for
subserous and 5.2 (SD+0.4) for cervical fibroid. The mean duration of menstral flow in the
studied subjects was 5.6 (SD+1.8)days.
29
Table 5 show the frequency distribution of the fibroid locations and their mean sizes.
Table 5: Showing the distribution of the fibroid location and their mean sizes.
Fibroid location Frequency % Mean Size
Submucus 15 19.7 42.3
Intramural 51 67.1 47.4
Subserous 5 6.6 81.6
Cervical 5 6.6 40.8
TOTAL 76 100.0
30
The mean value of the right renal length was 108.9 (SD+12.9)mm, while that of the left renal
length was 109.1(SD+13.8)mm. There was no statistical significance(p >0.05) difference
between the right and left renal length when the fibroid location and size were used to
compare.
31
Table 6 shows the distribution of the degree of calyceal dilation.
Table 6: The distribution of the degree of calyceal dilatation.
Degree of
calyceal
dilatation
Total Right kidney % Left kidney %
Grade 0 81 41 53.9 40 52.6
Grade 1 48 22 28.9 26 34.2
Grade 2 20 12 15.8 8 10.5
Grade 3 3 1 1.3 2 2.6
TOTAL 152 76 100.0 76 100.0
A total of 41(53.9%) patients had normal calyces on the right while 28.9%, 15.8%, and 1.3%
had grades 1,2, and 3 respectively.
There was a weak correlation (r=0.4) between the mean right calyceal dilation (RCD) of 0.6
(SD+0.8)mm and mean fibroid size of 48.2 (SD+20.8)mm in this study.
For the submucous fibroid and intramural fibroids, weak correlations (r=0.3 and r=0.4
respectively) exist between RCD and these locations.
Subserous fibriod has no correlation with RCD while a strong correlation (r=0.6) exists with
the cervical fibroid.
Right calyceal dilatation correlated strongly (r=0.7) with the cervical mean fibroid size of
40.8(SD+13.3)mm and weakly (r=0.3) with mean fibroid sizes of 42.3(SD+11.8)mm and
32
47.4(SD+2.1)mm in the submucous and intramural locations respectively. However, there is
no relationship between RCD and the subserous mean fibroid size of 81.6(SD+17.6)mm.
On the left side, a total of 40(52.6%) patients had normal calyces while 34.2%, 10.5%, and
2.6% had grades 1,2, and 3 respectively.
The mean left calyceal dilation (LCD) was 0.6(SD+0.8)mm and this showed a weak
correlation (r=0.3)with the fibroid mean size of 48.2(SD+20.8)mm in this study.
The submucous fibroid showed a negative correlation (r= -0.3) with LCD.
The correlation (r=0.2) between LCD and the intramural fibroid is weakly positive while the
subserous fibroid showed a strong correlation(r=0.8).
There was no correlation (r=0.0) between the cervical fibroid and LCD.
A similar pattern of relationship as for LCD and fibroid locations is seen when LCD is
correlated with mean fibroid sizes.
No correlation exist with the cervical mean fibroid size of 40.8(SD+13.3)mm but a very
strong correlation(r=0.8) with the mean fibroid size of 81.6(SD+17.6)mm for the subserous
fibroid.
A weak correlation(r=0.2) with the intramural fibroid size of 47.4(SD+21)mm and a weak
negative correlation (r=-0.3) relationship with LCD and the submucous fibroid mean size of
42.3(SD+11.8)mm is shown.
33
Table 7 shows the grouping of the measured renal parenchymal thickness on the right and
left.
Table 7: The groupings of renal parenchyma thickness on the right and left.
Renal
parenchyma
thickness(mm)
Total Right Kidney
(No of cases)
% Left Kidney
(No of cases)
%
8.0- 12.9 2 2 2.6 0 0
13.0-17.9 53 29 38.2 24 31.6
18.0-22.9 95 44 57.9 51 67.1
>/23 2 1 1.3 1 1.3
Total 152 76 100.0 76 100.0
The mean right parenchymal thickness (RPT) was 18.1(SD+2.7)mm and showed a weak non
correlation with the mean fibroid size of 48.2(SD+ 20.8)mm.
Similarly, in the submucous, subserous and intramural fibroids, the mean RPT of
18.4(SD+2.2)mm, 17.4(SD+2.1)mm and 16.7(SD+4.9)mm respectively showed no
correlation (r= -0.1, -0.1 and -0.2 respectively) with these locations.
The strongest negative correlation (r= -0.7)was observed in the cervical location.
There is no demonstrable correlation between RPT and the various mean fibroid sizes.
The mean Left parenchyma thickness (LPT) was 18.8(SD+2.4)mm and this also showed a
weak non correlation relationship with the fibroid mean size of 48.2(SD+20.8)mm.
Likewise, in the cervical, subserous and intramural fibroids, the mean LPT of
19.5(SD+2.0)mm, 21.0(SD+1.8)mm and 18.6(SD+2.5)mm respectively showed negative
correlation (r= -0.3 -0.7 and -0.2 respectively) with these locations.
A weak correlation (r= 0.3)was observed in the submucous location.
34
There was no demonstrable correlation between LPT and mean fibroid sizes for the
intramural, subserous and cervical fibroid, however a weak correlation of r=0.3 was seen
with the submucous mean fibroid size.
35
Table 8 shows the distribution of the degree of ureteral dilatation.
Table 8: The distribution of the degree of ureteral dilatation.
Degree of
ureteral
dilatation(mm)
Total Right ureter
(No of cases)
% Left ureter
(No of cases)
%
0 133 62 81.6 71 93.4
1 17 12 15.8 5 6.6
2 2 2 2.6 0 0.0
Total 152 76 100.0 76 100.0
The mean right ureteral dilation (RUD) for this study was 0.2(SD+0.5)mm with a weak
correlation(r=0.4) with the mean fibroid size.
There is a strong correlation(r= 0.8) between RUD mean value of 1.4(SD+0.5)mm and the
subserous fibroid.
The intramural and cervical fibroids showed weak correlations (r= 0.3 and 0.2 respectively)
with mean RUD values each of 0.2(SD+0.4)mm.
The mean sizes of the intramural, subserous and cervical fibroids correlated with RUD while
no correlation was seen with the submucous fibroid.
The mean Left ureteral dilation (LUD) for this study was 0.0(SD+0.2)mm and shows a weak
correlation (r= 0.1) with the mean fibroid size.
There were no correlations (r= 0.0) of LUD with the subserous, cervical and submucous
fibroid locations. Intramural fibroid location however, has a weak correlation (r=0.1).
The mean sizes of the submucous, subserous and cervical fibroids also showed no correlation
with LUD, with a weak correlation (r= 0.1) seen with the mean size of the intramural fibroid.
36
Table 9 is a summary of all the tables, giving a descriptive statistics for each fibroid location.
Table 9. Descriptive statistics of the fibroid location.
KEY:
RPT – Right Renal Parenchymal Thickness
LPT – Left Renal Parenchymal Thickness
RCD – Right Calyceal dilatation
LCD – Left Calyceal dilatation
RUD – Right Ureteral Dilatation
LUD – Left Ureteral Dilatation
FS – Fibroid size
n – Number of cases
Location of
fibroid
n Mean
age
(years)
Mean
Menarche
(years)
Mean
Parity
Mean
Menstral
flow (days)
Mean
Right
renal length
(mm)
Mean
Left
renal length
(mm)
Mean
RPT
(mm)
Mean
LPT
(mm)
Mean
RCD
(mm)
Mean
LCD
(mm)
Mean
RUD
(mm)
Mean
LUD
(mm)
Mean
FS
(mm)
Submucous 15 30.4 12.7 1.8 6.9 108.8 108.8 18.4 18.7 0.5 0.4 0.0 0.0 42.3
Intramural 51 34.4 13.5 2.2 5.1 109.4 109.5 18.3 18.6 0.6 0.5 0.2 0.0 47.4
Subserous 5 39.4 14.6 3.4 6.4 108.4 112.4 17.4 21.0 1.0 1.8 1.4 0.0 81.6
Cervical 5 32.6 13.0 2.0 5.2 104.8 102.3 16.7 19.5 1.0 1.0 0.2 0.0 40.8
37
DISCUSSION
Uterine fibroid is a disease of women in the reproductive age group, it affects women from
the age of 25years onwards1,5-7. The mean age in this study was 33.8years. The submucus
variety is seen to present at an earlier age (30.4years) and this may be attributed to its
association with increased menstrual flow7 which makes the patient present to her
gynaecologist early.
Women who smoke 10 sticks of cigarettes daily have been said to have an 18% decreased
risk for fibroids13, but this could not be corroborated as most women in this enviroment do
not smoke and none of the patients had smoked before.
The use of oral contraceptives for five consecutive years has also been reported to reduce the
risk for fibroid by 17%12. Only one patient in this study used oral contraceptives
consecutively for eight years she had an intramural fibroid. The patient probably had fibroid
before she started taking the pills or she is a deviation from the norm.
The patients were mostly of low parity.This finding is in agreement with common finding
that fibroids are common in nulliparous or low parity women26,50. However, no conclusive
theory has been attributed to this but, a hypothesis put forward is that myoma formation may
be viewed as a response to injury, potentially from hypoxia in myometrial cells during
menstruation7. Nulliparous and low parous women (para0-2) constituted the largest
percentage(57.9%) in this study. On the other hand, a significant number of the women
(32.9%) were of high parity (para four and above) in this study. This is similar to findings
from other Nigerian authors15,27, which reflects the fact that most Nigerian women marry
early and are already grandmultiparous by age 30years.
The size of fibroid varies from tiny microscopic size to uterine size corresponding to or
greater than 12 weeks gestation10. In this study, the smallest size encountered was about
22mm and largest about 109mm with a mean size of 48.2mm.
38
Intramural fibroid remains the commonest with 67.1% in this study. This agrees with
previous documentations1-3. The relative ease at which intramural fibroid are picked on
ultrasound scan makes it easier to diagnose.
Hydronephrosis and hydroureters of various degrees(Grades 1-3) were observed in this study,
this as earlier stated, is due to the close relationship of the distal ureters to the lateral vagina
fornix which causes compression with resultant impedance to the flow of urine. Ellenbogen
et al47, in their study, highlighted the value of ultrasound scan as an effective screening test in
patients with obstruction.
A general overview of this study population shows that about half of the patients had no
calyceal dilatation. Grade 1 dilatation was the commonly observed. False- positive result has
been observed to be commoner with ultrasound appearance of grade 1 hydronephrosis51 and
some of the explanation for this includes: normal variant, increased urine flow, acute and
chronic inflammation and renal cystic disease. This study tried to minimise a false positive
result by ensuring that the patients emptied their urinary bladder before evaluation of the
renal system and excluded patients with renal disease from the study.
On the right side, calyceal dilatation (RCD) was related to cervical, submucus and the
intramural fibroids in terms of their location and sizes.
Left calyceal dilatation (LCD) showed a strong relationship with subserous fibroid in terms
of location and size. A weak relationship exist with submucus and intramural fibroids.
Cervical fibroid had no relationship with LCD.
The small number of patients seen with subserous and cervical fibroids could account for the
outcome of result. Another attributable factor may be the presence of the fibroid mass on
either the left or right half of the uterus as demonstrated on a transverse pelvic ultrasound
scan.
It has been reported that in the presence of various degrees of hydronephrosis, the residual
parenchymal thickness serves as an important indicator of its severity49. Dilatation of the
pelvicalyceal collecting system leads to gradual thinning of the surrounding renal
parenchyma and if this is prolonged, can result in functional impairment. It is also possible to
have a hugely dilated pelvicalyceal system with an apparently thin but merely attenuated and
potentially normal rim of parenchyma on its periphery19 .
39
Most of the patients in this study had renal parenchyma thickness between 13.0 to 22mm.
The highest grade of hydronephrosis (Grade 3) was seen to be associated with a significant
reduction in renal parenchymal thickness.
Correlation of the right and left parenchyma thickness (RPT and LPT) with fibroid locations
showed no relationship with any of them. The mean fibroid sizes have no relationship with
parenchyma thickness as well.
These findings, in line with previous studies, demonstrate that it is the degree of
hydronephrosis rather than the fibroid location and size that determines the residual
parenchymal thickness49.
The ureters when not dilated are difficult to visualise on ultrasound with a maximum calibre
of about 3mm 2. An attempt has been made to grade ureteral dilatation into four groups and
this shows a large percentage (87.5%) to be in the grade 0 group. This can be due to
peristaltic waves propelling bolus of urine along the ureter thereby making visualization of
the ureters difficult.
Right ureter dilatation (RUD) was more commonly encountered and showed a stronger
relationship with location and size of uterine fibroid compared to left ureter dilatation.
It is however interesting to note that calyceal and ureteral dilatation were strongly related to
the cervical fibroid on the right in terms of location and size ; and subserous fibroid showed a
strong relationship with ureteral dilatation on the right in terms of location and size but was
related to left side in terms of calyceal dilatation. The intramural fibroid also showed some
relationship with ureteral dilatation on the right with regards to location and size.
Ultrasound is invaluable as a screening test in patients with renal tract obstruction. It is
cheap, readily available, non-hazardous and non-invasive.
Ultrasound has been used to demonstrate the relationship between various location and size
of fibroid mass and upper renal tract changes. It should therefore be the first line of
investigation rather than subject all patients with uterine fibroid to intravenous urography to
determine involvement of the renal system. This will reduce the hazard of ionizing radiation
and inconveniences that patients are exposed to when they undergo such procedure and also
be cheaper for the patient in terms of cost.
40
LIMITATIONS
The break down of the ultrasound scanning machine at the maternity wing of the Hospital
prevented patients from going the extra mile of coming down to the General wing of the
Hospital to have their scan done. This accounted largely for the limited number of patients, in
addition to strike actions by hospital staff during the period of the study.
41
SUMMARY
The findings in seventy-six (76) patients to determine the relationship between location and
size of uterine fibroid mass and upper renal tract changes using ultrasound in the University
of Ilorin Teaching Hospital between a period of one year (June 2004-June 2005) has been
presented.
The study has shown the relationship of epidemiological, obstetrics and gynaecological
history in relation to the location and size of uterine fibroid. The observed upper renal tract
changes have also been highlighted with correlation with different fibroid locations and sizes.
It revealed that calyceal and ureteral dilatation were strongly related to the cervical fibroid on
the right in terms of location and size while fibroid in the subserous layer also has this strong
relationship with ureteral dilatation on the right in terms of location and size; but was related
to the left side in terms of calyceal dilatation.
There was no preference in the occurrence of calyceal dilatation on either side in regards of
location and size of the intramural and submucus fibroid. However, the intramural fibroid
showed some relationship with ureteral dilatation on the right in regards to location and size.
Ultrasound has been found to be useful as a screening test in patients with upper renal tract
changes secondary to uterine fibroid and this should be the first line of investigation.
42
REFERENCES
1. Novak E.R. & Woodruff. Myoma and other Benign Tumors of the uterus in Novaks
Gynaecologic and Obstetric pathology with clinical and endocrine relations. 8th
edition WB Saunders Company Philadelphia. 1979;260-279.
2. Varma T R. Diseases of the uterus. In: Clinical Gynaecology. Edward Arnold, A
division of Hodder & Stoughton London. 1991;458-469.
3. Sutton CJG.Treatment of large uterine fibroid. Commentaries Brit.
J.Obstet.Gynaecol.1996:103;495-496.
4. Fletcher HM, Fredrick J.An update on the management of uterine fibroids.Africa
Health. 1999, 21:5-8.
5. Akinkugbe A. Fibroids and their complications. In: A textbook of obstetrics and
gynaecology. Evans Brothers (Nigeria Publishers) Ltd.1996; pg 382-392.
6. Buttram VC, Reiter RC. Uterine leiomyoma: etiology, symptomatology, and
management. Fertil Steril 1981; 36:433-445.
7. Stewart EA. Uterine fibroids. The Lancet. 2001, 357:293-298.
8. Kjeruff KH, Langenberg P, Seidman JD, Strolley PD, Guzinski GM. Uterine
leiomyomas: racial differences in severity, symptoms and age at diagnosis. J Reprod.
Med 1996; 41:483-490.
9. Marchall LM, Spiegelman D, Barbieri RL. variation in the incidence of uterine
leiomyoma among premenopausal women by age and race. Obstet Gynecol 1997;
90:967-973
10. Conley G. Lacey. Disorders of the uterine corpus. In: Benson, Current Obstetric &
Gynaecologic Diagnosis & treatment. 5th Edition. LANGE medical publications/Los
Altos California. 1984; pg 258-263.
11. Ross RK, Pike MC, Vessey MP, Bull D, Yeasts D, Casagrande JT. Risk factors for
uterine fibroids, reduced risks associated with contraceptives, Brit. Med. J. 1986;
293:359-362.
12. Paraziini FL Vecchia C, Negri E, Ceccheti G, Fedele L; Epidemiologic characteristics
of women with uterine fibroids: a case control study. Obstet Gynecol. 1988; 72:853-
857.
13. Vollenhoven BJ, Lawrence AS, Healy DL, Uterine fibroids: A clinical reviw. Brit. J.
Obstet. Gynaecol. 1990; 97:285-298.
43
14. Luoto R, Kaprio J; Rutanen EM; Taipale P; Perola M; Koskenwuo M. Heritability
and risk factors of uterine fibroids. The finnish twin cohort study. Maturitas. 2000;
37:15-26
15. Aboyeji AP, Ijaiya MA. Uterine fibroids: A ten year review in Ilorin, Nigeria. Nig. J.
Med. 2002; 11:16-19.
16. Salder TW. Urogenital system: In: Langman’s Medical Embryology; 6th Edition;
Williams & Wilkins. Baltimore. 1990; pp 260-279.
17. Ellis H. The Urinary Tract: In: Clinical Anatomy. Revised 7th Edition; Blackwell
Scientific Publications Oxford. 1983;125-133.
18. Ryan S.P. Mc Nicholas M.M.J. The Ureters: Anatomy for Diagnostic Imaging WB
Saunders Company Ltd, Philadelphia. 1994; pp 189-190.
19. O’Reilly P.H. Role of modern radiological investigations in Obstructive Uropathy,
Brit. Med. J. 1982; 284:1847-1851.
20. Conley G. Lancey. The female reproductive organs, The uterus: In: Benson, current
Obstetric & Gynaecologic diagnosis and management. 5th Edition. Lange medical
publications Los Altos. 1984;41-42.
21. Ibe-Lambert K. Ultrasound measurement of renal sizes in normal Nigerians. A study
carried out in LUTH. Dissersatation submitted to National Postgraduate Medical
College of Nigeria. 1991. pg 63-74.
22. Sanders R.C. Renal failure In: Clinical sonography. A practical Guide. Sanders R.C.
3rd Edition. Lippincott Philadelphia. 1984; pp 308-320.
23. Craner SF, Patel A. The frequency of uterine leiomyomas. Am J Clin Pathol. 1990; 9:
435-438.
24. Fletcher HM, Fredrick J. An update on the management of uterine fibroids. Africa,
Health 1999; 21: 5-8.
44
25. Uterine leiomyoma and adenomyomatosis In:Jones HW, Wentz AC and Burnett LS.
Novak’s Textbook of Gynaecology. 11th edition, Williams and Wilkins, Baltimore.
1998; pg 443-454.
26. Emenbolu JO; Uterine fibromyomata: Presentation and management in Northern
Nigeria. Int. Journal Gynaecol Obstet 1987; 25:414-416.
27. Ogunniyi SO, Fasuba O.B; Uterine fibromyomata. Nig. Med. Pract. 1990; 19:93-95.
28. Omu AE, Ihejerika IJ, Tabowel G. Management of uterine fibroids at the University
of Benin Teaching Hospital. Trop. Doct. 1984, 82-85.
29. Lowe DG. Benign tumors of the uterus In: Dewhurst’s Textbook of Obstetrics and
Gynaecology for Postgraduates. 6th Edition Edmonds DK Ed Blackwell Science
London 1999; 553-555.
30. Cesen-Cummings K; Walker CL; Davis BJ. Lessons from pregnancy and parturition;
uterine leiomyomas result from discordant differentiation and dedifferentiation
responses in smooth muscles cells. Med Hypotheses. 2000; 55; pg 485-490.
31. Balen AH. Secondary Amenorrhea. In: Dewhurst’s Textbook of Obstetrics and
Gynaecology for postgraduates 6th Edition. Edmonds DK Ed Blackwell Science
London 1999;42-60.
32. Linder D, Gartler SM. Glucose-6-phosphate dehydrogenase Mosaicism: utilization as
a cell marker in the study of leiomyomas Science. 1965; 150: 67-69.
33. Marshal RD, Fejzo ML, Friedman AJ, et al. Analysis of androgen receptor DNA
reveals the independent clonal origins of uterine leiomyoma and the secondary nature
of cytogenetic aberrations in the development of leiomyoma. Genes chromosomes
cancer 1994; 11:1-6.
34. Lees W.R, Highman J.H. Gynaecological Imaging In:Textbook of Radiology and
Imaging. Sutton D. 6th Edition Churchill Livingstone, Edinburgh. 1999;1242-1245.
45
35. Karasick S; Lev-Toaff AS; Toaff ME. Imaging of uterine leiomyomas. Am. J.
Roentgenol. 1992; 158: 799-805.
36. Briggs N.D. Uterine Fibroids. Trop. J. Obs. Gynae 1995; 12: 63-65.
37. Iloabachie G.C. Submucus Fibroid polyp of the uterus, an underrated cause of
morbidity and mortality. Trop. J. Obs. Gynae 1991; 8: 47-48.
38. Grossman TG, Compton AA. Recurrent premenstrual acute urinary retention due to
uterine myomas. J Reprod Med. 1978; 20:340-342.
39. Ogunbode O. Environmental factors in the management of uterine fibroids, Trop. J.
Obs. Gynae 1987; 2: 119-120.
40. Sanders R.C. Haematuria In: Clinical sonography. A practical guide. Sanders R.C. 3rd
Edition. 1984 Lippincott Philadelphia. 1984; pp 330-334.
41. Rose J.G; Gillenwater JY, Wyker AT. The recovery of function of chronically
obstructed and infected ureters; Invest. Urol. 1976; 13:125-130.
42. Naber KG, Madsen PO. Renal function during acute total ureteral occlusion and the
role of lymphatics; an experimental study in dogs. J. Urol 1973; 109:330-338.
43. Green J, Vardy Y, Munichor M, Better OS. Extreme unilateral hydronephrosis with
normal glomerular filtration rate: physiological study in a case of obstructive
uropathy. J. Urol. 1986; 136: 361-365.
44. Hatch D. A. Ultrasound of kidney with Hydronephrosis. http:meddean.luc.edu /
lumen / medical / urology / ushydro. Htm;1996.
45. Buck C, Macleod MA, Blacklock NJ. The advantage of 99mTc-DTPA in dynamic
renal scintigraphy and measurement of renal function. Br J Urol 1980; 52:174-187.
46. Dubovsky EV, Bueschen AJ, Tobin M, Scott JW, Tauxe WN. In: Hollenberg NK,
Lange S, eds. Radionuchides in nephrology. Stuttgart: Georg Thieme Verlag, 1980
46
47. Ellenbogen PH, Scheible FW, Talner LB, Leopold GR. Sensitivity of Gray scale
ultrasound in detecting urinary tarct obstruction. Am J Roentgenol. 1978; 130:731-
733.
48. Amis E.S, Harrman D.S.; Renal ultrasonography. A practical overview, Radiol. Clin.
North Am. 1984; 22:315-332.
49. Elyaderani MK; Gabriele OF. Ultrasound of renal masses: Sem. Ultrasound. 1981;
5:21-43.
50. Sriiteri PK, MacDonald PC. Role of extraglandular estrogen in human endocrinology
In: Green RO, Astwood E.B (ed.). Handbook of physiology; Washington D.C. Am
Physio-Society 1973; 615-616.
51. Kamholtz RG, Craven JJ, Dorfman GS. Obstruction and the minimally dilated renal
collecting system, Ultrasound evaluation. Radiology 1989; 170:51-53.