Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell Carcinoma

Renal cell carcinoma (RCC) is the predominant renal malignancy in adults. Of the four general subtypes, papillary renal cell carcinoma (P-RCC) is the second most common and can be subdivided into type I, type II, and a mixture of type I and II. Focal segmental glomerulosclerosis (FSGS) is the most c...

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Main Authors: Dominik Dabrowski, Ekin Ozluk, Silvia Barbeito, Eric X. Wei
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Case Reports in Pathology
Online Access:http://dx.doi.org/10.1155/2020/8811905
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author Dominik Dabrowski
Ekin Ozluk
Silvia Barbeito
Eric X. Wei
author_facet Dominik Dabrowski
Ekin Ozluk
Silvia Barbeito
Eric X. Wei
author_sort Dominik Dabrowski
collection DOAJ
description Renal cell carcinoma (RCC) is the predominant renal malignancy in adults. Of the four general subtypes, papillary renal cell carcinoma (P-RCC) is the second most common and can be subdivided into type I, type II, and a mixture of type I and II. Focal segmental glomerulosclerosis (FSGS) is the most common glomerulopathy at all ages, and it can be seen as a paraneoplastic syndrome. RCC, in general, is known to present with many paraneoplastic syndromes, and glomerulopathies are among these. Rarely, RCC and glomerulopathies may overlap in the same patient. Here, we report a 58-year-old male with a past medical history of FSGS and chronic kidney disease (CKD), stage III, who was found to have an incidental renal mass that was later diagnosed as type II P-RCC. The histology showed pseudostratified tumor cells with an eosinophilic cytoplasm that formed papillary configurations and displayed areas of necrosis. The prior FSGS diagnosis exhibited segmental sclerosis, refractory tufts, and capillary membrane wrinkling. A period of 1.5 years elapsed between the diagnosis of the glomerulopathy and the malignancy. The tumor was found to be at stage TIb. To our knowledge, this may be the first reported case of usual-type FSGS as paraneoplastic glomerulopathy (PG) preceding P-RCC. Because FSGS only sparingly affects the kidney and is a common glomerulopathy in adults, it is reasonable to complete comprehensive diagnostic studies and commence medically necessary treatment, especially in the background of other renal comorbidities. These preexisting comorbidities may be associated with malignancy very early in its course. The probability of RCC-associated paraneoplastic glomerulopathy is low, which means an already incidentally found renal mass may conceal a serpentine paraneoplastic syndrome. A more developed understanding of these manifestations can lead experienced clinicians to suspect and possibly uncover an insidious RCC before it advances.
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spelling doaj-art-0842e99e7b4f4e16b2859b20179fb15c2025-02-03T05:51:16ZengWileyCase Reports in Pathology2090-67812090-679X2020-01-01202010.1155/2020/88119058811905Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell CarcinomaDominik Dabrowski0Ekin Ozluk1Silvia Barbeito2Eric X. Wei3Department of Pathology and Translational Pathobiology, LSU Health Shreveport, USADepartment of Pathology and Translational Pathobiology, LSU Health Shreveport, USADepartment of Radiology, LSU Health Shreveport, USADepartment of Pathology and Translational Pathobiology, LSU Health Shreveport, USARenal cell carcinoma (RCC) is the predominant renal malignancy in adults. Of the four general subtypes, papillary renal cell carcinoma (P-RCC) is the second most common and can be subdivided into type I, type II, and a mixture of type I and II. Focal segmental glomerulosclerosis (FSGS) is the most common glomerulopathy at all ages, and it can be seen as a paraneoplastic syndrome. RCC, in general, is known to present with many paraneoplastic syndromes, and glomerulopathies are among these. Rarely, RCC and glomerulopathies may overlap in the same patient. Here, we report a 58-year-old male with a past medical history of FSGS and chronic kidney disease (CKD), stage III, who was found to have an incidental renal mass that was later diagnosed as type II P-RCC. The histology showed pseudostratified tumor cells with an eosinophilic cytoplasm that formed papillary configurations and displayed areas of necrosis. The prior FSGS diagnosis exhibited segmental sclerosis, refractory tufts, and capillary membrane wrinkling. A period of 1.5 years elapsed between the diagnosis of the glomerulopathy and the malignancy. The tumor was found to be at stage TIb. To our knowledge, this may be the first reported case of usual-type FSGS as paraneoplastic glomerulopathy (PG) preceding P-RCC. Because FSGS only sparingly affects the kidney and is a common glomerulopathy in adults, it is reasonable to complete comprehensive diagnostic studies and commence medically necessary treatment, especially in the background of other renal comorbidities. These preexisting comorbidities may be associated with malignancy very early in its course. The probability of RCC-associated paraneoplastic glomerulopathy is low, which means an already incidentally found renal mass may conceal a serpentine paraneoplastic syndrome. A more developed understanding of these manifestations can lead experienced clinicians to suspect and possibly uncover an insidious RCC before it advances.http://dx.doi.org/10.1155/2020/8811905
spellingShingle Dominik Dabrowski
Ekin Ozluk
Silvia Barbeito
Eric X. Wei
Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell Carcinoma
Case Reports in Pathology
title Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell Carcinoma
title_full Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell Carcinoma
title_fullStr Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell Carcinoma
title_full_unstemmed Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell Carcinoma
title_short Focal Segmental Glomerulosclerosis Preceding Type 2 Papillary Renal Cell Carcinoma
title_sort focal segmental glomerulosclerosis preceding type 2 papillary renal cell carcinoma
url http://dx.doi.org/10.1155/2020/8811905
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AT silviabarbeito focalsegmentalglomerulosclerosisprecedingtype2papillaryrenalcellcarcinoma
AT ericxwei focalsegmentalglomerulosclerosisprecedingtype2papillaryrenalcellcarcinoma