Primary <it>de novo </it>malignant giant cell tumor of kidney: a case report

<p>Abstract</p> <p>Background</p> <p>Osteoclast-like giant cell tumors are usually observed in osseous tissue or as tumors of tendon sheath, characterized by the presence of multinucleated giant cells and mononuclear stromal cells. It has been reported in various extrao...

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Main Authors: Torkian Bahman, Kanthan Rani
Format: Article
Language:English
Published: BMC 2004-06-01
Series:BMC Urology
Online Access:http://www.biomedcentral.com/1471-2490/4/7
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spelling doaj-4f3133392e8745a581def12ccf8ef8862020-11-25T00:20:20ZengBMCBMC Urology1471-24902004-06-0141710.1186/1471-2490-4-7Primary <it>de novo </it>malignant giant cell tumor of kidney: a case reportTorkian BahmanKanthan Rani<p>Abstract</p> <p>Background</p> <p>Osteoclast-like giant cell tumors are usually observed in osseous tissue or as tumors of tendon sheath, characterized by the presence of multinucleated giant cells and mononuclear stromal cells. It has been reported in various extraosseous sites including breast, skin, soft tissue, salivary glands, lung, pancreas, female genital tract, thyroid, larynx and heart. However, extraosseus occurrence of such giant cell tumors in the kidney is extremely rare and is usually found in combination with a conventional malignancy. De-novo primary malignant giant cell tumors of the kidney are unusual lesions and to our knowledge this is the second such case.</p> <p>Case Presentation</p> <p>We report a rare case of extraosseous primary denovo malignant giant cell tumor of the renal parenchyma in a 39-year-old Caucasian female to determine the histogenesis of this neoplasm with a detailed literature review.</p> <p>Conclusion</p> <p>Primary <it>denovo </it>malignant giant cell tumor of the kidney is extremely rare. The cellular origin of this tumor is favored to be a pluripotential mesenchymal stromal cell of the mononuclear/phagocytic cellular lineage. Awareness of this neoplasm is important in the pathological interpretation of unusual findings at either fine needle aspiration or frozen section of solid renal masses.</p> http://www.biomedcentral.com/1471-2490/4/7
collection DOAJ
language English
format Article
sources DOAJ
author Torkian Bahman
Kanthan Rani
spellingShingle Torkian Bahman
Kanthan Rani
Primary <it>de novo </it>malignant giant cell tumor of kidney: a case report
BMC Urology
author_facet Torkian Bahman
Kanthan Rani
author_sort Torkian Bahman
title Primary <it>de novo </it>malignant giant cell tumor of kidney: a case report
title_short Primary <it>de novo </it>malignant giant cell tumor of kidney: a case report
title_full Primary <it>de novo </it>malignant giant cell tumor of kidney: a case report
title_fullStr Primary <it>de novo </it>malignant giant cell tumor of kidney: a case report
title_full_unstemmed Primary <it>de novo </it>malignant giant cell tumor of kidney: a case report
title_sort primary <it>de novo </it>malignant giant cell tumor of kidney: a case report
publisher BMC
series BMC Urology
issn 1471-2490
publishDate 2004-06-01
description <p>Abstract</p> <p>Background</p> <p>Osteoclast-like giant cell tumors are usually observed in osseous tissue or as tumors of tendon sheath, characterized by the presence of multinucleated giant cells and mononuclear stromal cells. It has been reported in various extraosseous sites including breast, skin, soft tissue, salivary glands, lung, pancreas, female genital tract, thyroid, larynx and heart. However, extraosseus occurrence of such giant cell tumors in the kidney is extremely rare and is usually found in combination with a conventional malignancy. De-novo primary malignant giant cell tumors of the kidney are unusual lesions and to our knowledge this is the second such case.</p> <p>Case Presentation</p> <p>We report a rare case of extraosseous primary denovo malignant giant cell tumor of the renal parenchyma in a 39-year-old Caucasian female to determine the histogenesis of this neoplasm with a detailed literature review.</p> <p>Conclusion</p> <p>Primary <it>denovo </it>malignant giant cell tumor of the kidney is extremely rare. The cellular origin of this tumor is favored to be a pluripotential mesenchymal stromal cell of the mononuclear/phagocytic cellular lineage. Awareness of this neoplasm is important in the pathological interpretation of unusual findings at either fine needle aspiration or frozen section of solid renal masses.</p>
url http://www.biomedcentral.com/1471-2490/4/7
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