Primary thoracic neuroblastoma in an adult: A rare case report
Neuroblastoma is one of the most common malignant tumors in childhood, which mainly occurs in adrenal glands and peripheral sympathetic nerve system. Neuroblastoma occurring in adulthood is rare, and adults with neuroblastoma arising from thorax are exceedingly rare. A case of neuroblastoma that ori...
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Veröffentlicht in: | Medicine (Baltimore) 2019-07, Vol.98 (30), p.e16564-e16564 |
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description | Neuroblastoma is one of the most common malignant tumors in childhood, which mainly occurs in adrenal glands and peripheral sympathetic nerve system. Neuroblastoma occurring in adulthood is rare, and adults with neuroblastoma arising from thorax are exceedingly rare. A case of neuroblastoma that originated from thorax was reported, and was treated by resection operation.
A 46-year-old woman was admitted to our hospital with left side chest pain for 5 days. Laboratory examinations were all normal. Chest computerized tomogram (CT) showed a lesion with clear boundary that was located at the left dorsal pleura. The nature of the mass was heterogeneous, showing slight heterogeneous enhancement after contrast and there was no obvious necrosis.
Based on the morphologic and immunohistochemical features, the tumor diagnosis was favorable for neuroblastoma.
A resection operation was carried out.
Three years postoperative, no sign of recurrence or metastasis has been observed.
Primary neuroblastoma in adulthood is rare and has poor prognosis. Resection can be an important treatment option, and combining with other methods like chemotherapy, stem cell transplantation, the survival rate may be improved. |
doi_str_mv | 10.1097/MD.0000000000016564 |
format | Article |
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A 46-year-old woman was admitted to our hospital with left side chest pain for 5 days. Laboratory examinations were all normal. Chest computerized tomogram (CT) showed a lesion with clear boundary that was located at the left dorsal pleura. The nature of the mass was heterogeneous, showing slight heterogeneous enhancement after contrast and there was no obvious necrosis.
Based on the morphologic and immunohistochemical features, the tumor diagnosis was favorable for neuroblastoma.
A resection operation was carried out.
Three years postoperative, no sign of recurrence or metastasis has been observed.
Primary neuroblastoma in adulthood is rare and has poor prognosis. Resection can be an important treatment option, and combining with other methods like chemotherapy, stem cell transplantation, the survival rate may be improved.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000016564</identifier><identifier>PMID: 31348281</identifier><language>eng</language><publisher>United States: the Author(s). Published by Wolters Kluwer Health, Inc</publisher><subject>Clinical Case Report ; Female ; Humans ; Middle Aged ; Neuroblastoma - pathology ; Neuroblastoma - surgery ; Thoracic Neoplasms - pathology ; Thoracic Neoplasms - surgery ; Thoracic Surgical Procedures - methods ; Treatment Outcome</subject><ispartof>Medicine (Baltimore), 2019-07, Vol.98 (30), p.e16564-e16564</ispartof><rights>the Author(s). Published by Wolters Kluwer Health, Inc.</rights><rights>Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3556-6cc5acac48b8510b2deb4f054ba4601d5a10c5d3e10cf5097186849819dc33ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709284/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709284/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31348281$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tan, Yan-Bin</creatorcontrib><creatorcontrib>Li, Jin-Fan</creatorcontrib><creatorcontrib>Li, Wen-Shan</creatorcontrib><creatorcontrib>Yang, Run-Lin</creatorcontrib><title>Primary thoracic neuroblastoma in an adult: A rare case report</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>Neuroblastoma is one of the most common malignant tumors in childhood, which mainly occurs in adrenal glands and peripheral sympathetic nerve system. Neuroblastoma occurring in adulthood is rare, and adults with neuroblastoma arising from thorax are exceedingly rare. A case of neuroblastoma that originated from thorax was reported, and was treated by resection operation.
A 46-year-old woman was admitted to our hospital with left side chest pain for 5 days. Laboratory examinations were all normal. Chest computerized tomogram (CT) showed a lesion with clear boundary that was located at the left dorsal pleura. The nature of the mass was heterogeneous, showing slight heterogeneous enhancement after contrast and there was no obvious necrosis.
Based on the morphologic and immunohistochemical features, the tumor diagnosis was favorable for neuroblastoma.
A resection operation was carried out.
Three years postoperative, no sign of recurrence or metastasis has been observed.
Primary neuroblastoma in adulthood is rare and has poor prognosis. Resection can be an important treatment option, and combining with other methods like chemotherapy, stem cell transplantation, the survival rate may be improved.</description><subject>Clinical Case Report</subject><subject>Female</subject><subject>Humans</subject><subject>Middle Aged</subject><subject>Neuroblastoma - pathology</subject><subject>Neuroblastoma - surgery</subject><subject>Thoracic Neoplasms - pathology</subject><subject>Thoracic Neoplasms - surgery</subject><subject>Thoracic Surgical Procedures - methods</subject><subject>Treatment Outcome</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkElPwzAQhS0EgrL8AiSUI5eAdyccKqGWTaKCA5wtx5nSgBsXO6Hi32Mou2VppPE3b54fQvsEHxFcquPJ-Aj_HCKF5GtoQASTuSglX0cDjKnIVan4FtqO8TFBTFG-ibYYYbygBRmg4W1o5ia8Zt3MB2Mbm7XQB185Ezs_N1nTZibdunfdSXaaBRMgsyZCFmDhQ7eLNqbGRdj7rDvo_vzsbnSZX99cXI1Or3PLhJC5tFYYaywvqkIQXNEaKj7FgleGS0xqYQi2omaQylSkz5FCFrwsSFlbxiywHTRc6S76ag61hbYLxunFyrz2ptF_X9pmph_8i5YKl7TgSeDwUyD45x5ip-dNtOCcacH3UVMqhVIq5ZNQtkJt8DEGmH6vIVi_J68nY_0_-TR18Nvh98xX1AngK2DpXQchPrl-CUHPwLhu9qEnVElzikmJFZU4f-9I9gY6zo4U</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Tan, Yan-Bin</creator><creator>Li, Jin-Fan</creator><creator>Li, Wen-Shan</creator><creator>Yang, Run-Lin</creator><general>the Author(s). Published by Wolters Kluwer Health, Inc</general><general>Wolters Kluwer Health</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190701</creationdate><title>Primary thoracic neuroblastoma in an adult: A rare case report</title><author>Tan, Yan-Bin ; Li, Jin-Fan ; Li, Wen-Shan ; Yang, Run-Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3556-6cc5acac48b8510b2deb4f054ba4601d5a10c5d3e10cf5097186849819dc33ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Clinical Case Report</topic><topic>Female</topic><topic>Humans</topic><topic>Middle Aged</topic><topic>Neuroblastoma - pathology</topic><topic>Neuroblastoma - surgery</topic><topic>Thoracic Neoplasms - pathology</topic><topic>Thoracic Neoplasms - surgery</topic><topic>Thoracic Surgical Procedures - methods</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tan, Yan-Bin</creatorcontrib><creatorcontrib>Li, Jin-Fan</creatorcontrib><creatorcontrib>Li, Wen-Shan</creatorcontrib><creatorcontrib>Yang, Run-Lin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tan, Yan-Bin</au><au>Li, Jin-Fan</au><au>Li, Wen-Shan</au><au>Yang, Run-Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary thoracic neuroblastoma in an adult: A rare case report</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>98</volume><issue>30</issue><spage>e16564</spage><epage>e16564</epage><pages>e16564-e16564</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>Neuroblastoma is one of the most common malignant tumors in childhood, which mainly occurs in adrenal glands and peripheral sympathetic nerve system. Neuroblastoma occurring in adulthood is rare, and adults with neuroblastoma arising from thorax are exceedingly rare. A case of neuroblastoma that originated from thorax was reported, and was treated by resection operation.
A 46-year-old woman was admitted to our hospital with left side chest pain for 5 days. Laboratory examinations were all normal. Chest computerized tomogram (CT) showed a lesion with clear boundary that was located at the left dorsal pleura. The nature of the mass was heterogeneous, showing slight heterogeneous enhancement after contrast and there was no obvious necrosis.
Based on the morphologic and immunohistochemical features, the tumor diagnosis was favorable for neuroblastoma.
A resection operation was carried out.
Three years postoperative, no sign of recurrence or metastasis has been observed.
Primary neuroblastoma in adulthood is rare and has poor prognosis. Resection can be an important treatment option, and combining with other methods like chemotherapy, stem cell transplantation, the survival rate may be improved.</abstract><cop>United States</cop><pub>the Author(s). Published by Wolters Kluwer Health, Inc</pub><pmid>31348281</pmid><doi>10.1097/MD.0000000000016564</doi><oa>free_for_read</oa></addata></record> |
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subjects | Clinical Case Report Female Humans Middle Aged Neuroblastoma - pathology Neuroblastoma - surgery Thoracic Neoplasms - pathology Thoracic Neoplasms - surgery Thoracic Surgical Procedures - methods Treatment Outcome |
title | Primary thoracic neuroblastoma in an adult: A rare case report |
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