5q Minus Myelodysplasia Associated with Multiple Epithelioid Granulomas within Conventional Renal Cell Carcinoma

A 69-year-old Caucasian female, with a previous diagnosis of 5q minus myelodysplastic syndrome, presented with conventional renal cell carcinoma (RCC) associated with multiple-epithelioid nonnecrotizing granulomas. Two previous reports of sarcoidosis, primarily involving the lung and skin, have been...

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Main Authors: Rahul G. Matnani, Roshan K. Patel, Stephen E. Strup, Rouzan G. Karabakhtsian
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Case Reports in Pathology
Online Access:http://dx.doi.org/10.1155/2012/138126
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author Rahul G. Matnani
Roshan K. Patel
Stephen E. Strup
Rouzan G. Karabakhtsian
author_facet Rahul G. Matnani
Roshan K. Patel
Stephen E. Strup
Rouzan G. Karabakhtsian
author_sort Rahul G. Matnani
collection DOAJ
description A 69-year-old Caucasian female, with a previous diagnosis of 5q minus myelodysplastic syndrome, presented with conventional renal cell carcinoma (RCC) associated with multiple-epithelioid nonnecrotizing granulomas. Two previous reports of sarcoidosis, primarily involving the lung and skin, have been described in patients with 5q minus myelodysplasia. A cluster of closely linked genes encoding for cytokines such as IL-4, IL-5, and IL-3 are present on chromosome 5q. Hence, in sarcoidosis, cytokine imbalances associated with the deletion of these cytokine genes have been postulated. However, an occurrence of epithelioid granulomas within a carcinoma, in preexisting clonal myelodysplastic syndrome, has not been described. The patient, in the current study, had long standing 5q minus deletion, clinically characterized by refractory anemia associated with hypolobated megakaryocytes. However, the patient's history was negative for sarcoidosis and the extensive nonnecrotizing epithelioid granulomas were confined within RCC. Due to the absence of Th-2 cytokines, such as IL-4 and IL-5, in a subset of 5q minus myelodysplastic syndrome, proinflammatory Th-1 cytokines such as IFN-γ and TNF-α may be exaggerated in an environment conducive to antigen expression. Hence, we propose a greater susceptibility for the development of granulomas, at least in a subset of patients with 5q minus myelodysplasia.
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spelling doaj-art-313d381e677243e497ffad22fa603b3e2025-08-20T03:55:01ZengWileyCase Reports in Pathology2090-67812090-679X2012-01-01201210.1155/2012/1381261381265q Minus Myelodysplasia Associated with Multiple Epithelioid Granulomas within Conventional Renal Cell CarcinomaRahul G. Matnani0Roshan K. Patel1Stephen E. Strup2Rouzan G. Karabakhtsian3Department of Pathology and Laboratory Medicine, College of Medicine, Chandler Medical Center, University of Kentucky, 800 Rose Street, Lexington, KY 40536-0298, USADepartment of Pathology and Laboratory Medicine, College of Medicine, Chandler Medical Center, University of Kentucky, 800 Rose Street, Lexington, KY 40536-0298, USADivision of Urology, Department of Surgery, College of Medicine, Chandler Medical Center, University of Kentucky, 800 Rose Street, Lexington, KY 40536-0293, USADepartment of Pathology and Laboratory Medicine, College of Medicine, Chandler Medical Center, University of Kentucky, 800 Rose Street, Lexington, KY 40536-0298, USAA 69-year-old Caucasian female, with a previous diagnosis of 5q minus myelodysplastic syndrome, presented with conventional renal cell carcinoma (RCC) associated with multiple-epithelioid nonnecrotizing granulomas. Two previous reports of sarcoidosis, primarily involving the lung and skin, have been described in patients with 5q minus myelodysplasia. A cluster of closely linked genes encoding for cytokines such as IL-4, IL-5, and IL-3 are present on chromosome 5q. Hence, in sarcoidosis, cytokine imbalances associated with the deletion of these cytokine genes have been postulated. However, an occurrence of epithelioid granulomas within a carcinoma, in preexisting clonal myelodysplastic syndrome, has not been described. The patient, in the current study, had long standing 5q minus deletion, clinically characterized by refractory anemia associated with hypolobated megakaryocytes. However, the patient's history was negative for sarcoidosis and the extensive nonnecrotizing epithelioid granulomas were confined within RCC. Due to the absence of Th-2 cytokines, such as IL-4 and IL-5, in a subset of 5q minus myelodysplastic syndrome, proinflammatory Th-1 cytokines such as IFN-γ and TNF-α may be exaggerated in an environment conducive to antigen expression. Hence, we propose a greater susceptibility for the development of granulomas, at least in a subset of patients with 5q minus myelodysplasia.http://dx.doi.org/10.1155/2012/138126
spellingShingle Rahul G. Matnani
Roshan K. Patel
Stephen E. Strup
Rouzan G. Karabakhtsian
5q Minus Myelodysplasia Associated with Multiple Epithelioid Granulomas within Conventional Renal Cell Carcinoma
Case Reports in Pathology
title 5q Minus Myelodysplasia Associated with Multiple Epithelioid Granulomas within Conventional Renal Cell Carcinoma
title_full 5q Minus Myelodysplasia Associated with Multiple Epithelioid Granulomas within Conventional Renal Cell Carcinoma
title_fullStr 5q Minus Myelodysplasia Associated with Multiple Epithelioid Granulomas within Conventional Renal Cell Carcinoma
title_full_unstemmed 5q Minus Myelodysplasia Associated with Multiple Epithelioid Granulomas within Conventional Renal Cell Carcinoma
title_short 5q Minus Myelodysplasia Associated with Multiple Epithelioid Granulomas within Conventional Renal Cell Carcinoma
title_sort 5q minus myelodysplasia associated with multiple epithelioid granulomas within conventional renal cell carcinoma
url http://dx.doi.org/10.1155/2012/138126
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AT stephenestrup 5qminusmyelodysplasiaassociatedwithmultipleepithelioidgranulomaswithinconventionalrenalcellcarcinoma
AT rouzangkarabakhtsian 5qminusmyelodysplasiaassociatedwithmultipleepithelioidgranulomaswithinconventionalrenalcellcarcinoma