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Culturing of Retinal Pigment Epithelial Cells on an Ex Vivo Model of Aged Human Bruch's Membrane
Published on: April 12, 2018
Fundus changes in (type II) mesangiocapillary glomerulonephritis simulating drusen: a histopathological report
J Duvall-Young1, M K MacDonald, N M McKechnie
1Princess Alexandra Eye Pavilion, Royal Infirmary, Edinburgh.
The British Journal of Ophthalmology
|April 1, 1989
Summary
Histopathological examination revealed kidney-like deposits in the eye of a patient with dense deposit disease. This finding offers new insights into the ocular manifestations of this rare glomerulonephritis.
Area of Science:
- Ophthalmology
- Nephrology
- Pathology
Background:
- Type II mesangiocapillary glomerulonephritis, also known as dense deposit disease, is a rare kidney disorder.
- The characteristic renal lesion involves electron-lucent deposits within the glomerular basement membrane.
Observation:
- Histopathological examination of the eye in a patient with dense deposit disease was performed.
- The study focused on identifying any ocular manifestations related to the underlying condition.
Findings:
- For the first time, deposits morphologically similar to those pathognomonic for dense deposit disease in the kidney were found in Bruch's membrane of the eye.
- The clinical fundus appearance mimicked that of drusen, commonly seen in age-related macular degeneration.
Implications:
- This discovery suggests a potential systemic involvement of dense deposit disease beyond the kidneys.
- Understanding these ocular findings may lead to earlier diagnosis and improved management strategies for patients.
- Further research is warranted to elucidate the exact nature and origin of these deposits in Bruch's membrane.
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