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Extraskeletal Mesenchymal Chondrosarcoma of Central Nervous System - A Rare but Aggressive Tumor: Analysis of Five Cases
Background: Extraskeletal mesenchymal chondrosarcoma (MCS) of the central nervous system (CNS) is extremely rare. Herein, we present the clinicopathological features of five CNS extraskeletal MCS. Material and Methods: Over the past 10 years, five cases of CNS MCS have been retrieved from in the arc...
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Published in: | Neurology India 2022-01, Vol.70 (1), p.285-288 |
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description | Background: Extraskeletal mesenchymal chondrosarcoma (MCS) of the central nervous system (CNS) is extremely rare. Herein, we present the clinicopathological features of five CNS extraskeletal MCS.
Material and Methods: Over the past 10 years, five cases of CNS MCS have been retrieved from in the archives of histopathology department. All biopsies were stained with vimentin, S-100, CD99, desmin, GFAP, INI1, WT1, STAT6, and EMA.
Results: There were four males and one female patient in the age group of 1.5-35 years. The clinical and radiological impression was meningioma in three cases, glomus jugulare and primitive neuroectodermal tumor in one case each. All showed classic biphasic morphology, areas of undifferentiated small blue round cells sharply demarcated from the island of cartilage. Three patients experienced multiple recurrences and died subsequently.
Conclusion: Extraskeletal MCS of CNS is rare and favors children and young adults. They show aggressive behavior and tend to recur despite surgery and radiotherapy. |
doi_str_mv | 10.4103/0028-3886.338726 |
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Material and Methods: Over the past 10 years, five cases of CNS MCS have been retrieved from in the archives of histopathology department. All biopsies were stained with vimentin, S-100, CD99, desmin, GFAP, INI1, WT1, STAT6, and EMA.
Results: There were four males and one female patient in the age group of 1.5-35 years. The clinical and radiological impression was meningioma in three cases, glomus jugulare and primitive neuroectodermal tumor in one case each. All showed classic biphasic morphology, areas of undifferentiated small blue round cells sharply demarcated from the island of cartilage. Three patients experienced multiple recurrences and died subsequently.
Conclusion: Extraskeletal MCS of CNS is rare and favors children and young adults. They show aggressive behavior and tend to recur despite surgery and radiotherapy.</description><identifier>ISSN: 0028-3886</identifier><identifier>EISSN: 1998-4022</identifier><identifier>DOI: 10.4103/0028-3886.338726</identifier><language>eng</language><publisher>Mumbai: Wolters Kluwer India Pvt. Ltd</publisher><subject>Bone cancer ; Brain cancer ; Case studies ; Central nervous system diseases ; Chondrosarcoma ; Nervous system ; Rare diseases</subject><ispartof>Neurology India, 2022-01, Vol.70 (1), p.285-288</ispartof><rights>COPYRIGHT 2022 Medknow Publications and Media Pvt. Ltd.</rights><rights>2022. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c444e-6e875154ea90fd2cf9a036d855810c5a2eeb317d0df20c41f180da13045bd4a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2635195887?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25751,27922,27923,37010,44588</link.rule.ids></links><search><creatorcontrib>Chatterjee, Debajyoti</creatorcontrib><creatorcontrib>Radotra, Bishan</creatorcontrib><creatorcontrib>Madan, Renu</creatorcontrib><creatorcontrib>Gupta, Sunil</creatorcontrib><title>Extraskeletal Mesenchymal Chondrosarcoma of Central Nervous System - A Rare but Aggressive Tumor: Analysis of Five Cases</title><title>Neurology India</title><description>Background: Extraskeletal mesenchymal chondrosarcoma (MCS) of the central nervous system (CNS) is extremely rare. Herein, we present the clinicopathological features of five CNS extraskeletal MCS.
Material and Methods: Over the past 10 years, five cases of CNS MCS have been retrieved from in the archives of histopathology department. All biopsies were stained with vimentin, S-100, CD99, desmin, GFAP, INI1, WT1, STAT6, and EMA.
Results: There were four males and one female patient in the age group of 1.5-35 years. The clinical and radiological impression was meningioma in three cases, glomus jugulare and primitive neuroectodermal tumor in one case each. All showed classic biphasic morphology, areas of undifferentiated small blue round cells sharply demarcated from the island of cartilage. Three patients experienced multiple recurrences and died subsequently.
Conclusion: Extraskeletal MCS of CNS is rare and favors children and young adults. They show aggressive behavior and tend to recur despite surgery and radiotherapy.</description><subject>Bone cancer</subject><subject>Brain cancer</subject><subject>Case studies</subject><subject>Central nervous system diseases</subject><subject>Chondrosarcoma</subject><subject>Nervous system</subject><subject>Rare diseases</subject><issn>0028-3886</issn><issn>1998-4022</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkU1v1DAQhiMEEkvhztES5yz-TBxuIWqhUgEJytnyOuNtuklcPEm3--9xtBSotPLB9vh5RrbfLHvL6FoyKt5TynUutC7WQuiSF8-yFasqnUvK-fNs9ff4ZfYK8TZthWB8lT2cP0zR4g56mGxPvgDC6G4OQ1o3N2FsY0AbXRgsCZ40MCa4J18h3ocZyY8DTjCQnNTku41ANvNE6u02AmJ3D-R6HkL8QOrR9gfscOlwsdQbi4Cvsxfe9ghv_sxn2c-L8-vmc3717dNlU1_lTkoJeQG6VExJsBX1LXe-slQUrVZKM-qU5QAbwcqWtp5TJ5lnmraWCSrVppVWirPs3bHvXQy_ZsDJ3IY5piuh4YVQrFJal_-ore3BdKMP6aFu6NCZuqiULHVVVonKT1BbGCH9ShjBd6n8hF-f4NNoYejcSYEeBZf-HSN4cxe7wcaDYdQsMZslR7PkaI4xJ-XjUdmHfoKIu37eQzQDtLsx7J94-X-e4VqZx-zFb4AErgk</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Chatterjee, Debajyoti</creator><creator>Radotra, Bishan</creator><creator>Madan, Renu</creator><creator>Gupta, Sunil</creator><general>Wolters Kluwer India Pvt. 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Herein, we present the clinicopathological features of five CNS extraskeletal MCS.
Material and Methods: Over the past 10 years, five cases of CNS MCS have been retrieved from in the archives of histopathology department. All biopsies were stained with vimentin, S-100, CD99, desmin, GFAP, INI1, WT1, STAT6, and EMA.
Results: There were four males and one female patient in the age group of 1.5-35 years. The clinical and radiological impression was meningioma in three cases, glomus jugulare and primitive neuroectodermal tumor in one case each. All showed classic biphasic morphology, areas of undifferentiated small blue round cells sharply demarcated from the island of cartilage. Three patients experienced multiple recurrences and died subsequently.
Conclusion: Extraskeletal MCS of CNS is rare and favors children and young adults. They show aggressive behavior and tend to recur despite surgery and radiotherapy.</abstract><cop>Mumbai</cop><pub>Wolters Kluwer India Pvt. Ltd</pub><doi>10.4103/0028-3886.338726</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bone cancer Brain cancer Case studies Central nervous system diseases Chondrosarcoma Nervous system Rare diseases |
title | Extraskeletal Mesenchymal Chondrosarcoma of Central Nervous System - A Rare but Aggressive Tumor: Analysis of Five Cases |
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