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Primary low‐grade neuroendocrine carcinoma of the skin: An exceedingly rare entity
Low‐grade neuroendocrine tumors (NETs), also known as carcinoid tumor, commonly arise from the gastrointestinal (GI) and pulmonary tracts, but rarely occur in the skin. Cutaneous NET typically occurs as metastases or high‐grade primary lesions, called Merkel cell carcinoma. In the few cases describe...
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Published in: | Journal of cutaneous pathology 2017-11, Vol.44 (11), p.978-981 |
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description | Low‐grade neuroendocrine tumors (NETs), also known as carcinoid tumor, commonly arise from the gastrointestinal (GI) and pulmonary tracts, but rarely occur in the skin. Cutaneous NET typically occurs as metastases or high‐grade primary lesions, called Merkel cell carcinoma. In the few cases described in literature, primary low‐grade neuroendocrine carcinomas of the skin (LGNECS) are usually indolent cutaneous nodules, presenting on the head and trunk of elderly patients. LGNECS tumors are histologically similar to its counterparts arising in other anatomic locations. As there is no NET cut‐off for the skin due to their rarity, the GI scale was used instead; low‐grade NETs have a Ki‐67 proliferative index of less than 3%. The distinction between primary and metastatic NET, however, is not absolute and can be difficult. A primary vs metastatic NET diagnosis relies on clinical exclusion of a NET in other, more common, anatomic locations. Here, we present a case of an LGNECS on the scalp of a 72‐year‐old female patient. Whole body imaging failed to identify any octreotide‐avid lesions elsewhere in the patient, aside from 2 positive cervical lymph nodes, which were confirmed with a node dissection and histologic evaluation. This is the 19th reported case of LGNECS and the 2nd reported case of LGNECS with nodal metastasis. |
doi_str_mv | 10.1111/cup.13028 |
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Cutaneous NET typically occurs as metastases or high‐grade primary lesions, called Merkel cell carcinoma. In the few cases described in literature, primary low‐grade neuroendocrine carcinomas of the skin (LGNECS) are usually indolent cutaneous nodules, presenting on the head and trunk of elderly patients. LGNECS tumors are histologically similar to its counterparts arising in other anatomic locations. As there is no NET cut‐off for the skin due to their rarity, the GI scale was used instead; low‐grade NETs have a Ki‐67 proliferative index of less than 3%. The distinction between primary and metastatic NET, however, is not absolute and can be difficult. A primary vs metastatic NET diagnosis relies on clinical exclusion of a NET in other, more common, anatomic locations. Here, we present a case of an LGNECS on the scalp of a 72‐year‐old female patient. Whole body imaging failed to identify any octreotide‐avid lesions elsewhere in the patient, aside from 2 positive cervical lymph nodes, which were confirmed with a node dissection and histologic evaluation. This is the 19th reported case of LGNECS and the 2nd reported case of LGNECS with nodal metastasis.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/cup.13028</identifier><identifier>PMID: 28815668</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Carcinoid Tumor - pathology ; cutaneous carcinoid ; Female ; Geriatrics ; Humans ; low‐grade neuroendocrine carcinomas of the skin ; Lymph nodes ; Lymphatic Metastasis - pathology ; Metastases ; Metastasis ; neuroendocrine skin ; Neuroendocrine tumors ; Nodules ; Octreotide ; primary cutaneous neuroendocrine ; Scalp ; Scalp - pathology ; Skin ; Skin cancer ; Skin Neoplasms - pathology ; Tumors</subject><ispartof>Journal of cutaneous pathology, 2017-11, Vol.44 (11), p.978-981</ispartof><rights>2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3868-934283a7b672c098869c83d86905698533b93cc67bca6b1be29e9a8b9822922e3</citedby><cites>FETCH-LOGICAL-c3868-934283a7b672c098869c83d86905698533b93cc67bca6b1be29e9a8b9822922e3</cites><orcidid>0000-0002-7982-5253</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28815668$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Tiffany Y.</creatorcontrib><creatorcontrib>Morrison, Annie O.</creatorcontrib><creatorcontrib>Susa, Joe</creatorcontrib><creatorcontrib>Cockerell, Clay J.</creatorcontrib><title>Primary low‐grade neuroendocrine carcinoma of the skin: An exceedingly rare entity</title><title>Journal of cutaneous pathology</title><addtitle>J Cutan Pathol</addtitle><description>Low‐grade neuroendocrine tumors (NETs), also known as carcinoid tumor, commonly arise from the gastrointestinal (GI) and pulmonary tracts, but rarely occur in the skin. Cutaneous NET typically occurs as metastases or high‐grade primary lesions, called Merkel cell carcinoma. In the few cases described in literature, primary low‐grade neuroendocrine carcinomas of the skin (LGNECS) are usually indolent cutaneous nodules, presenting on the head and trunk of elderly patients. LGNECS tumors are histologically similar to its counterparts arising in other anatomic locations. As there is no NET cut‐off for the skin due to their rarity, the GI scale was used instead; low‐grade NETs have a Ki‐67 proliferative index of less than 3%. The distinction between primary and metastatic NET, however, is not absolute and can be difficult. A primary vs metastatic NET diagnosis relies on clinical exclusion of a NET in other, more common, anatomic locations. Here, we present a case of an LGNECS on the scalp of a 72‐year‐old female patient. Whole body imaging failed to identify any octreotide‐avid lesions elsewhere in the patient, aside from 2 positive cervical lymph nodes, which were confirmed with a node dissection and histologic evaluation. This is the 19th reported case of LGNECS and the 2nd reported case of LGNECS with nodal metastasis.</description><subject>Aged</subject><subject>Carcinoid Tumor - pathology</subject><subject>cutaneous carcinoid</subject><subject>Female</subject><subject>Geriatrics</subject><subject>Humans</subject><subject>low‐grade neuroendocrine carcinomas of the skin</subject><subject>Lymph nodes</subject><subject>Lymphatic Metastasis - pathology</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>neuroendocrine skin</subject><subject>Neuroendocrine tumors</subject><subject>Nodules</subject><subject>Octreotide</subject><subject>primary cutaneous neuroendocrine</subject><subject>Scalp</subject><subject>Scalp - pathology</subject><subject>Skin</subject><subject>Skin cancer</subject><subject>Skin Neoplasms - pathology</subject><subject>Tumors</subject><issn>0303-6987</issn><issn>1600-0560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kLtOwzAUhi0EoqUw8ALIEhNDWl8ax2arKm5SJTq0s-U4pyUldYqTqGTjEXhGngRDgI2z_Mun75zzI3ROyZCGGdlmN6ScMHmA-lQQEpFYkEPUJ5zwSCiZ9NBJVW0IoUKK-Bj1mJQ0FkL20WLu863xLS7K_cfb-9qbDLCDxpfgstL63AG2xtvclVuDyxWunwBXz7m7xhOH4dUCZLlbFy32xgMGV-d1e4qOVqao4OwnB2h5e7OY3kezx7uH6WQWWS6FjBQfM8lNkoqEWaKkFMpKnoUI9ysZc54qbq1IUmtESlNgCpSRqZKMKcaAD9Bl59358qWBqtabsvEurNRUxWwsOYvHgbrqKOvLqvKw0rvuZ02J_upPh_70d3-BvfgxNukWsj_yt7AAjDpgnxfQ_m_S0-W8U34CsIx5mw</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Chen, Tiffany Y.</creator><creator>Morrison, Annie O.</creator><creator>Susa, Joe</creator><creator>Cockerell, Clay J.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</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>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><orcidid>https://orcid.org/0000-0002-7982-5253</orcidid></search><sort><creationdate>201711</creationdate><title>Primary low‐grade neuroendocrine carcinoma of the skin: An exceedingly rare entity</title><author>Chen, Tiffany Y. ; Morrison, Annie O. ; Susa, Joe ; Cockerell, Clay J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3868-934283a7b672c098869c83d86905698533b93cc67bca6b1be29e9a8b9822922e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Carcinoid Tumor - pathology</topic><topic>cutaneous carcinoid</topic><topic>Female</topic><topic>Geriatrics</topic><topic>Humans</topic><topic>low‐grade neuroendocrine carcinomas of the skin</topic><topic>Lymph nodes</topic><topic>Lymphatic Metastasis - pathology</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>neuroendocrine skin</topic><topic>Neuroendocrine tumors</topic><topic>Nodules</topic><topic>Octreotide</topic><topic>primary cutaneous neuroendocrine</topic><topic>Scalp</topic><topic>Scalp - pathology</topic><topic>Skin</topic><topic>Skin cancer</topic><topic>Skin Neoplasms - pathology</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Tiffany Y.</creatorcontrib><creatorcontrib>Morrison, Annie O.</creatorcontrib><creatorcontrib>Susa, Joe</creatorcontrib><creatorcontrib>Cockerell, Clay J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of cutaneous pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Tiffany Y.</au><au>Morrison, Annie O.</au><au>Susa, Joe</au><au>Cockerell, Clay J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary low‐grade neuroendocrine carcinoma of the skin: An exceedingly rare entity</atitle><jtitle>Journal of cutaneous pathology</jtitle><addtitle>J Cutan Pathol</addtitle><date>2017-11</date><risdate>2017</risdate><volume>44</volume><issue>11</issue><spage>978</spage><epage>981</epage><pages>978-981</pages><issn>0303-6987</issn><eissn>1600-0560</eissn><abstract>Low‐grade neuroendocrine tumors (NETs), also known as carcinoid tumor, commonly arise from the gastrointestinal (GI) and pulmonary tracts, but rarely occur in the skin. Cutaneous NET typically occurs as metastases or high‐grade primary lesions, called Merkel cell carcinoma. In the few cases described in literature, primary low‐grade neuroendocrine carcinomas of the skin (LGNECS) are usually indolent cutaneous nodules, presenting on the head and trunk of elderly patients. LGNECS tumors are histologically similar to its counterparts arising in other anatomic locations. As there is no NET cut‐off for the skin due to their rarity, the GI scale was used instead; low‐grade NETs have a Ki‐67 proliferative index of less than 3%. The distinction between primary and metastatic NET, however, is not absolute and can be difficult. A primary vs metastatic NET diagnosis relies on clinical exclusion of a NET in other, more common, anatomic locations. Here, we present a case of an LGNECS on the scalp of a 72‐year‐old female patient. Whole body imaging failed to identify any octreotide‐avid lesions elsewhere in the patient, aside from 2 positive cervical lymph nodes, which were confirmed with a node dissection and histologic evaluation. This is the 19th reported case of LGNECS and the 2nd reported case of LGNECS with nodal metastasis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>28815668</pmid><doi>10.1111/cup.13028</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-7982-5253</orcidid></addata></record> |
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subjects | Aged Carcinoid Tumor - pathology cutaneous carcinoid Female Geriatrics Humans low‐grade neuroendocrine carcinomas of the skin Lymph nodes Lymphatic Metastasis - pathology Metastases Metastasis neuroendocrine skin Neuroendocrine tumors Nodules Octreotide primary cutaneous neuroendocrine Scalp Scalp - pathology Skin Skin cancer Skin Neoplasms - pathology Tumors |
title | Primary low‐grade neuroendocrine carcinoma of the skin: An exceedingly rare entity |
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