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An interesting case of hemiparesis
Prof.Dr.G.Sundaramurthy’s unit
-Dr.K.Senthamizh selvan
CLINICAL SCENARIO• Venkatesan
• 40yrs /male
• kanchipuram
• manual labourer
Presenting complaints :
- weakness of left UL,LL
- slurring of speech for past 10
days
HISTORY OF PRESENT ILLNESS• H/O weakness of left UL and LL for the past
10 days ,insidious onset ,progressive in nature H/O difficulty in raising his arm H/O difficulty in buttoning his shirts H/O difficulty in climbing stairs H/O difficulty in holding his slippers • No H/O difficulty in turning side to side in
bed,or getting up from bed • No H/O diminished/altered perception of
clothes,hot & cold objects
• No H/O of unsteadiness or fall while washing his face
• No H/O involuntary movements
• No H/O disturbance in memory,emotional changes
• No H/O altered smell perception
• No H/O diminished visual perception
• No H/O double vision
• No H/O impaired sensation over face
• No H/O difficulty in mastication
• H/O of deviation of angle of mouth to R side associated with slurring of speech
• No H/O of hard of hearing ,tinnitus ,giddiness
• H/O difficulty in swallowing food , associated with nasal regurgitation
• No H/O of change in voice
• No H/O difficulty in turning head to opposite side or shrugging shoulders
• No H/O difficulty in moving the tongue
• No H/O bladder and bowel disturbance
• H/O headache ,diffuse ,dull in character ,not associated with blurring of vision ,vomiting ,no postural variation ,no aggravating and relieving factors.
• No H/O fever , seizures , recent head trauma
• No H/O chest pain,palpitation , breathlessness, syncope
PAST HISTORY Not a K/C SHT,DM,PT,CAHD,RHD,epileptic
PERSONAL HISTORY :
• Mixed diet
• occasional smoker and alcoholic
FAMILY HISTORY :
Not contributory
ON EXAMINATION • Conscious
• Responds to simple commands
• Emaciated
• Afebrile
• Hydration fair
• pallor+/icterus-/cyanosis-/clubbing-/PE-
• No SGLA
• Vitals : BP-110/70 mmHg
PR-88/min ,regular
-- Papulo-nodular skin lesions with excoriations seen over arm, fore arm,trunk,back,medial aspect of thigh----suggestive of extensive scabies ? NORWEGIAN
SYSTEM EXAMINATION
• CVS: S1,S2+
No Murmur
• RS: NVBS +
No added sounds
• P/A : soft
No HSM
BS+
CNS EXAMINATON
HIGHER MENTAL FUNCTION:
- conscious
- oriented
- memory intact
- no emotional disturbance
CRANIAL NERVES
NERVE RIGHT LEFT
1 N N
2 -Visual acuity,field of vision & fundus
N N
3,4,6 EOM pupils
Full4 mm,reacting
Full4 mm,reacting
5 N N
7 N UMN palsy
8 N N
9,10 Gag&uvular movements impaired
Gag&uvular movements impaired
11 N N
12 N Deviated to left side
MOTOR SYSTEM RIGHT LEFT
Bulk N N
Tone UL LL
NN
Increased
Power UL LL
5/55/5
2/52/5
DTR ++ +++
Superficial reflexes + -
Plantar Flexor Extensor
SENSORY SYSTEM : all modalities clinically
normal
CEREBELLUM: could not be tested
NO meningeal signs
spine and cranium : normal
Problems
• Left hemiparesis,left UMN facial palsy
• B/L LMN 9&10th weakness
• LEFT LMN 12th nerve weakness
• Extensive scabetic lesions ? NORWEGIAN
IMPRESSION :
-CVA with brain stem involvement
- Demyelinating disease
- Retroviral disease
INVESTIGATIONS CBC : TC – 9800 cells/cumm DC- 56/40/4 ESR-25mm/hr Hb- 9 gm/dl MCV-82fl MCHC-30g/dl Platelet count -1.2lakh/cummRFT: Blood sugar-134 mg/dl Blood urea-24.8mg/dl S.creatinine-0.9mg/dl
S.Electrolytes : Na+ 130 K+ 4.4 Cl- 98 HCO3 - 23LFT: T.Bilirubin-1.2 D.Bilirubin-0.4 SGOT/SGPT-44/36 SAP-120ECG- ---WNL
X-RAY
CT BRAIN -CONTRAST
FINDINGS
----Thin walled cystic lesions in L frontal and B/L parietal lobe
----Enhancement of wall with central necrosis
----Eccentric target sign +
• Sputum AFB : Negative
• Mantoux :negative • HIV ELISA: POSITIVE
• VDRL: Non reactive • USG abdomen –no HSM, no intra abdominal lymphadenopathy
• ECHO: No RWMA Normal LV systolic function
• CSF analysis :
cell count – 50cells/cumm
lymphocytic predominance
total protein -110mg /dl
glucose -44mg/dl
ADA –low titres
Cob web –absent
TOXOPLASMA SEROLOGY :
IgG antibody positive in hightitres>500IU/L.
IgM- 1wk to 1month ,rarely 1 year,
-Typically absent in reactivated disesae
IgG-1month , persists life long,
-In its absence infection is less likely
Problems • Rapidly progressing neurological signs;
• Multiple ring enhancing lesions in CT brain
• HIV-ELISA positivity
• Toxoplasma antibody positivity
Further approach to our patient
• Neurophysician opinion : -Retroviral disease -CNS toxoplasmosis -To consider the possibility of tuberculoma • Dermatologist opinion for extensive scabies : -T.ivermectin 200mic/kg - 5%permethrin lotion
• Pt was registered in ART centre ,GSH CD4 count :96 cells/cumm
TREATMENT GIVEN - Inj. Mannitol 175ml iv tds - Inj.Lasix 20mg iv bd - T.pyrimethamine 100mg/d loading dose,followed by 50mg/d - T.sulfadiazine 4g/d - T.folic acid 10mg/d - T.septran DS 1BD -supportive care -physiotherapy
-Patient improved symptomatically after 5 days
-He was discharged at his request,advised to review after 6 weeks
REPEAT CT AFTER 6 WEEKS
TOXOPLASMA Vs TUBERCULOMA
Favouring toxoplasma
• M C ring enhancing lesions
in HIV (50-70%)
• Toxoplasma serology +
• clinical response to treatment
• Rapid radiological clearance
Against tuberculoma
• No past H/O of PT,ATT
• Normal chest x-ray
• Normal USG abd
• Sputum AFB ,Mantoux -ve
• CSF :AFB –ve
absent cob web
ADA in low titres
• Rapid radiological clearance
FINAL DIAGNOSIS
RETRO VIRAL DISEASE
CEREBRAL TOXOPLASMOSIS NORWEGIAN SCABIES
• Pt was started on ART
• Along with maintenance dose of
T.pyrimethamine 25mg/d
T.sulfadiazine 2g/d
T.folic acid 10mg/d
T.septran DS 1od
• Referred to GHTM, Tambaram for further follow up ,as per his wish.
TOXOPLASMOSIS
• Toxoplasma gondii-protozoan parasite
• Definitive host-felines
• Intermediate host-humans ,mammals
• asymptomatic –in immuno competent
• symptomatic –AIDS,congenital toxoplasmosis
• Reactivation syndrome -10 times common in
pts with antibody to organism(underlying immune compromise reactivates latent infection)
Life cycle
Human infection
Humans enter life cycle of t.gondii
Ingesting meat infected with tissue cysts
Ingesting food contaminated with infectious oocyst(cat feces)
transplacental transmission
infected organ transplantation
blood transfusion
CLINICAL FEATURES
• In Immuno competent:
-asymptomatic
-symptomatic(fever,lymphadenopathy
non specific rash)
- rarely chorio-retinitis
CONGENITAL TOXOPLASMOSIS
Toxoplasmosis acquired
Immuno-competant Immuno-compromised
Prior to pregnancy No risk Moderate risk
During pregnancy Mild risk Maximum risk
• Infected babies -75%--no symptoms -15%--chorioretinitis -10% --CNS symptoms• Features : Fever Lymphadenopathy Encephalitis seizures Anemia Microcephaly Non specific skin rash.
IMMUNO COMPROMISED ADULTS usually present with:• head ache • fever • seizures• focal deficits• ataxia• cognitive dysfunction• neuro psychiatric manifestations• visual disturances
Unusual presentations :
-myocarditis
-pneumonitis
-disseminated toxoplasmosis
WORK UP
• Base line investigations
• Toxoplasma serology:
• SABIN –FELDMAN DYE TEST: -sensitive &specific neutralization test -detects IgG antibody• Detection of toxoplasma antigen in body
fluids by ELISA• IFA,IHA,Double sandwich IgM ELISA • PCR : - demonstrates genome in body fluids,
CSF,amniotic fluid,BAL. -40% sensitive in CSF.
• CSF analysis: -mild mono nuclear pleocytosis -increased protein -low glucose -IgG antibody • CT BRAIN –contrast Can show single lesion• MRI brain-more sensitive -multiple lesions ,MC sites basal
ganglia and cortico medullary junction -single lesion –suspect diagnosis
ECCENTRIC TARGET SIGN
• MR-spectroscopy
• Tissue diagnosis
TREATMENT
• Immuno compromised
• Immuno competant:
Asymptomatic , age <5
symptomatic
pregnancy
vital organ dysfunction
OP TREATMENT: - Immuno competent - ocular toxoplasmosisIP TREATMENT: -Immuno compromised -CNS toxoplasmosis -Toxoplasmic pneumonitis/myocarditis -Disseminated toxoplasmosis
TREATMENT OPTIONS :
for 6 wks
Drugs Initial therapy for 6 wks
maintenance
pyrimethamine 100mg loading dose,50mg/d
25mg/d
sulfadiazine 4g/d 2g/d
Folinic acid 10mg/d 10mg/d
• In case of sulfa allergy :(sulfadiazine replaced )
-tmp 5mg/kg+smx 25mg/kg od
-clindamycin 600mg tds
-dapsone 100mg od
-atovaquone 750 mg qid
• In case of seizures – carbamazepine and phenytoin
In Pregnancy
Drugs Amniotic fluid antibody + Amniotic fluid antibody -
Spiramycin 1g po tds 1g po tds
Pyrimethamine 50mg/d 25mg/d
sulfadiazine 4g/d 3g/d
Folinic acid 10mg/d 10mg/d
Treatment duration
---- maintenance regimen is continued till patient’s CD4 count is >200 for 6 continuous months , while on ART
Role of steroids
Steriods are indicated if :
- midline shift
-increased ICT
- rapid deterioration within 48 hrs
Primary prophylaxis
In immunocompromised• If CD4 <100• Toxoplasma antibody –negative -----primary prophylaxis for toxoplasmosis
is to be given tmp(10mg/kg/d)+smx(50mg/kg/d) ------can be discontinued if CD> 200 for 3
continuous months ,while on ART
Health advise
• Immuno compromised • sero negative for toxoplasma
- proper cooking of meat -washing vegetables -personal hygiene
Carry home points
• Toxoplasmosis is the most common cause for SOL brain in HIV
• Most common cause for FND in HIV
• All HIV pts should have baseline screening for toxoplasma
• Negative serology--- consider other causes ,though it doesn’t R/O the disease
• IgM antibody not useful in HIV setting • Health advise and primary prophylaxis –prevents the disease.
THANK YOU