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Diagnose This (July 13,2020)

Fabry's disease, myelosomes, zebra bodies, X linked disease
What is your diagnosis?   The electron microscopic image depicts a podocyte with numerous myeloid bodies, myelinosomes, or "zebra" bodies as they are also known. This finding, taken in concert with the patient's clinical history was compatible with Fabry's disease. By light microscopy, a characteristic finding is the lacy, or foamy cytoplasm of the podocytes due to the lipid inclusions composed of globotriaosylceramide. Additionally, toluidine blue sections can be extremely helpful in identifying these inclusions. Fabry's disease is classified as a lysosomal storage disease caused by a deficiency in the alpha-galactosidase, an enzyme leading to the accumulation of globotriaosylceramide (GL3)...

Art of Medicine: Fabry

Fabry & Myelinosomes, Art of Medicine
The image above shows myelinosomes, also known as “zebra bodies” for their appearance on tangential sectioning.  Myelinosomes are seen in Fabry disease, a rare x-linked recessive genetic disorder caused by the defective activity of the enzyme alpha-galactosidase A.   Renal, cardiac, and cerebrovascular involvement is common and can be fatal by the 4th decade without enzyme replacement therapy.   Alpha galactosidase A deficiency results in accumulation of globotriaosylceramide within podocytes of glomeruli, tubules, myocytes, and endothelium.  Globotriaosylceramide accumulation results in the formation of myelinosomes. Since myelinosomes are lipid-derived, they are maintained on osmium fixation, but are lost with exposure to xylenes in...

Pushing Glass (March 23, 2018)

A-galactosidase A , pushing glass, arkana laboratories, kidney disease
These images are from the kidney biopsy of a 70-year-old woman with a history of hypertension and valvular heart disease presenting with renal failure and serum creatinine of 4 mg/dl. The findings are suggestive of a mutation in which of the following genes: A. Podocin B. Glucocerebrosidase C. a-galactosidase A D. Nephrin E. Phospholipase C Answer: C The images highlight podocytes loaded with numerous myelinosomes. There are only a few causes that can cause such accumulation, most notably Fabry disease. However, rare secondary causes to be considered include drugs such as chloroquine and chloroquine-like drugs (e.g., Plaquenil), amiodarone, aminoglycoside antibiotics,...

Fabry Disease in Female Carriers

A renal biopsy was performed on a 51 year old female with strong family history of Fabry disease and a known carrier of an alpha-glycosidase gene (GLA) pathogenic variant. At the time of the biopsy, the patient had no renal or extrarenal manifestations. The biopsy shows glomeruli with prominent visceral epithelial cells (podocytes) displaying ample vacuolated cytoplasm (Fig 1, H&E; Fig 2, Jones). Furthermore, electron microscopy shows numerous large, lamellated lipid vacuoles (myeloid bodies or zebra bodies) within the podocytes, characteristic of Fabry disease (Fig 3). Fabry disease is an X-linked disorder caused by GLA mutation and the resulting deficiency...

Fabry EM

Electron photomicrograph of a glomerular podocyte showing the characteristic electron dense laminated inclusions of Fabry disease. Fabry is a lysosomal storage disease with X-linked inheritance. Mutations in the gene for the enzyme alpha galactosidase A (GLA) result in accumulation of a glycolipid known as globotriaosylceramide (GL-3) in tissues including the kidney.