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Native and transplant kidney pathology
Case 8
Erik Heyerdahl StrømDept. of Pathology
Oslo University Hospital RikshospitaletOslo, Norway
ECP Helsinki 30 August 2011
Clinical historyCaucasian male 22 years.
• mild edema of lower extremities• hematuria• proteinuria, increasing to nephrotic level• moderate hypertension• slightly reduced renal function
Suspicion of chronic glomerulonephritisKidney biopsy was performed
PAS
Silver staining
Silver staining
Biopsy diagnosis
Glomerular lipid-containing deposits
suggestive of
Lecithin:cholesterol acyltransferase (LCAT) deficiency
Clinical follow-up
• Lipid metabolism:– Very low HDL, low LDL, elevated cholesterol
and triglycerides
• Corneal opacities
Genetic testing
Compound heterozygous:
Two mutations (R244H and M252K)
in exon 6 of the LCAT-gene, located on chromosome 16.
Final diagnosis: Familial LCAT-deficiency
Familial LCAT deficiency
Familial LCAT deficiency
• autosomal recessive disease
• due to a defect in esterification of plasma cholesterol– severe reduction of HDL– elevation of free cholesterol, triglycerides and
phospholipids
Familial LCAT deficiency
lipid-containing depositions within several organs:
• kidney– proteinuria, renal failure
• cornea– decreased vision
• erythrocytes– anemia due to defect of cytoplasmic membrane
• aorta and muscular arteries– premature atherosclerotic vascular disease?
Familial LCAT deficiencyGenetics
>70 different mutations described
Familial LCAT deficiency
Milder disease (”Fish-eye disease”)
Kluivenhoven JA: J Lipid Res 2004
”Fish eye”
Corneal opacities:
* multiple small greyish spots “foggy” discoloration; band-like at the periphery
* impaired vision
* present from early childhood in LCAT deficiency
Cornea in LCAT disease
Cornea in LCAT disease
Pathogenesis of renal lesion
• Heterogeneous lesions may be due to several mechanisms of disease
– deposition of different types of lipid containing molecules, incl. abnormal lipoproteins: Lipoprotein X (Lp-X)
– capillary wall impairment
– complement activation?
Differential diagnosis
• renal lesions in chronic liver diseases– ”hepatic glomerulosclerosis” (Sagaguchi H 1965)– Alagilles’s syndrome (hypoplasia of intrahepatic
bile ducts)
• other lipidoses
Case history
• Transplanted at 28 yrs, 6 yrs after initial diagnosis
• Received kidney from his father, who was heterozygous for LCAT mutation
Two days after transplantation
Biopsy proven acute rejection Banff IA
Biopsy two days after transplantation
Protocol biopsy 6 weeks after transplantation
CD 68
Protocol biopsy one year after transplantation
Recurrence of LCAT deficiency in renal graft
• Documented in graft
- 7 weeks after transplantation
- more than 5 years graft survival
What is the significance of the changes in the 2 days post transplant biopsy?
1) Unspecific changes?- probably not
2) Donor derived changes?- probably not
3) Recurrence of disease?- most likely
Why present this case?
Ultrastructural morphology is quite suggestive of LCAT-deficiency
Early recurrence in transplant
Coworkers:
Dr. Ståle Sund, Dept. of Pathology, Førde CentralHospital, Norway
Dr. Morten Reier-Nilsen, Dept. of Medicine, Drammen Hospital, Norway
Dr. Christina Dørje, Dept. of Nephrology, Oslo University Hospital, Norway
Dr. Trond P. Leren, Dept. of Medical Genetics, Oslo University Hospital, Norway
Ultrastruct Pathol 2011:35: 139–45