Print ISSN: 2581-5725
Online ISSN: 2456-9267
CODEN : IACHCL
IP Archives of Cytology and Histopathology Research (ACHR) open access, peer-reviewed quarterly journal publishing since 2016 and is published under the Khyati Education and Research Foundation (KERF), is registered as a non-profit society (under the society registration act, 1860), Government of India with the vision of various accredited vocational courses in healthcare, education, paramedical, yoga, publication, teaching and research activity, with the aim of faster and better dissemination of knowledge, we will be publishing the article more...Case Report
Author Details :
Volume : 5, Issue : 3, Year : 2020
Article Page : 244-247
https://doi.org/10.18231/j.achr.2020.053
Abstract
Renal replacement lipomatosis (RRL) is a rare condition that occurs as an end result of renal atrophy or replacement of renal parenchyma by excessive lipomatous tissue in renal sinus and perinephric space. We reported a case of RRL presented in our tertiary health centre. Left Nephrectomy was performed kidney sent to our department for histopathology examination and after extensive literature search, a diagnosis of RRL was given. In majority of cases, RRL is associated with renal calculi. Idiopathic variety of RRL is not common. It is a rare entity and due to lack of experience the diagnosis may be missed. It has to be differentiated from other fat-containing tumors such as xanthogranulomatous pyelonephritis, renal lipomas, liposarcoma and angiomyolipoma.
Keywords: RRL (Renal Replacement Lipomatosis), Idiopathic, Nephrectomy, Adipose tissue.
How to cite : Khatrri J, Sanwalka M, Gupta S, Sakarwal N , Awasthi S, Renal replacement lipomatosis - A rare but also underdiagnosed entity. IP Arch Cytol Histopathol Res 2020;5(3):244-247
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