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Arch Iran Med. 2020;23(6): 409-411.
doi: 10.34172/aim.2020.35
  Abstract View: 222
  PDF Download: 73

Case Report

Collagenofibrotic Glomerulopathy: Report a Rare Case

Rakesh Agarwal 1 * , Rashmi Baid 2, Jotideb Mukhopadhyay 1

1 Institute of Post-Graduate Medical Education and Research and Seth Sukhlal Karnani Memorial Hospital, Kolkata, India
2 Lilavati Hospital & Research Centre, Mumbai, India
*Corresponding Author: Rakesh Agarwal, 243, G.T Road(N), Laxmi Niketan, Flat-2E, Liluah, Howrah-711204, Email: dr.agarwal.rakesh@hotmail.com

Abstract

Collagenofibrotic glomerulopathy is a rare clinical entity with fewer than 40 cases reported worldwide. We describe a case of adult onset nephrotic syndrome with partial villous atrophy of the intestine who was diagnosed with this rare entity. Collagenofibrotic glomerulopathy is characterized by subendothelial and mesangial collagen type III deposition and increased procollagen III peptide levels. Extra renal involvement has been described in the form of hypertension, anemia and microangiopathic hemolytic anemia but villous atrophy has not been associated with this condition so far, possibly reflecting the paucity of literature. We describe this case and review the condition in this report.
Keywords: Collaagenofibrotic glomerulopathy, Nephrotic syndrome
Cite this article as: Agarwal R, Baid R, Mukhopadhyay J. Collagenofibrotic glomerulopathy: report a rare case. Arch Iran Med. 2020;23(6):409–411. doi: 10.34172/aim.2020.35.
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Submitted: 29 Jul 2018
Accepted: 11 Feb 2019
ePublished: 01 Jun 2020
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