Collagenofibrotic glomerulopathy: a systemic disease

T Yasuda, H Imai, Y Nakamoto, H Ohtani… - American journal of …, 1999 - Elsevier
T Yasuda, H Imai, Y Nakamoto, H Ohtani, A Komatsuda, H Wakui, AB Miura
American journal of kidney diseases, 1999Elsevier
Collagenofibrotic glomerulopathy is a recently discovered entity that is characterized by
massive accumulation of spiraled and frayed collagen fibrils in mesangial and
subendothelial areas, and elevated serum levels of procollagen III peptide. We report the
autopsy of a patient who received continuous ambulatory peritoneal dialysis (CAPD) therapy
for 7 years. Autopsy disclosed that massive accumulation of peculiar collagen fibers was
found not only in the kidney, but also in many organs including spleen, liver, myocardium …
Collagenofibrotic glomerulopathy is a recently discovered entity that is characterized by massive accumulation of spiraled and frayed collagen fibrils in mesangial and subendothelial areas, and elevated serum levels of procollagen III peptide. We report the autopsy of a patient who received continuous ambulatory peritoneal dialysis (CAPD) therapy for 7 years. Autopsy disclosed that massive accumulation of peculiar collagen fibers was found not only in the kidney, but also in many organs including spleen, liver, myocardium, and thyroid gland. Although the possibility remains that CAPD for 7 years might change or aggravate the deposition of abnormal collagen, the current case suggests a possibility that collagenofibrotic glomerulopathy is a systemic disorder with abnormal metabolism of type III collagen.
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