Intraepidermal Merkel cell carcinoma: A case series of a rare entity with clinical follow up
Background Merkel cell carcinoma (MCC) is a rare but aggressive cutaneous carcinoma. MCC typically involves dermis and although epidermotropism has been reported, MCC strictly intraepidermal or in situ (MCCIS) is exceedingly rare. Most of the cases of MCCIS described so far have other associated les...
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Veröffentlicht in: | Journal of cutaneous pathology 2017-08, Vol.44 (8), p.684-691 |
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creator | Jour, George Aung, Phyu P. Rozas‐Muñoz, Eduardo Curry, Johnathan L. Prieto, Victor Ivan, Doina |
description | Background
Merkel cell carcinoma (MCC) is a rare but aggressive cutaneous carcinoma. MCC typically involves dermis and although epidermotropism has been reported, MCC strictly intraepidermal or in situ (MCCIS) is exceedingly rare. Most of the cases of MCCIS described so far have other associated lesions, such as squamous or basal cell carcinoma, actinic keratosis and so on. Herein, we describe 3 patients with MCC strictly in situ, without a dermal component.
Methods
Our patients were elderly. 2 of the lesions involved the head and neck area and 1 was on a finger. All tumors were strictly intraepidermal in the diagnostic biopsies, and had histomorphologic features and an immunohistochemical profile supporting the diagnosis of MCC. Excisional biopsies were performed in 2 cases and failed to reveal dermal involvement by MCC or other associated malignancies.
Results and Conclusion
Our findings raise the awareness that MCC strictly in situ does exist and it should be included in the differential diagnosis of Paget's or extramammary Paget's disease, pagetoid squamous cell carcinoma, melanoma and other neoplasms that typically show histologically pagetoid extension of neoplastic cells. Considering the limited number of cases reported to date, the diagnosis of isolated MCCIS should not warrant a change in management from the typical MCC. |
doi_str_mv | 10.1111/cup.12966 |
format | Article |
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Merkel cell carcinoma (MCC) is a rare but aggressive cutaneous carcinoma. MCC typically involves dermis and although epidermotropism has been reported, MCC strictly intraepidermal or in situ (MCCIS) is exceedingly rare. Most of the cases of MCCIS described so far have other associated lesions, such as squamous or basal cell carcinoma, actinic keratosis and so on. Herein, we describe 3 patients with MCC strictly in situ, without a dermal component.
Methods
Our patients were elderly. 2 of the lesions involved the head and neck area and 1 was on a finger. All tumors were strictly intraepidermal in the diagnostic biopsies, and had histomorphologic features and an immunohistochemical profile supporting the diagnosis of MCC. Excisional biopsies were performed in 2 cases and failed to reveal dermal involvement by MCC or other associated malignancies.
Results and Conclusion
Our findings raise the awareness that MCC strictly in situ does exist and it should be included in the differential diagnosis of Paget's or extramammary Paget's disease, pagetoid squamous cell carcinoma, melanoma and other neoplasms that typically show histologically pagetoid extension of neoplastic cells. Considering the limited number of cases reported to date, the diagnosis of isolated MCCIS should not warrant a change in management from the typical MCC.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/cup.12966</identifier><identifier>PMID: 28543532</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Basal cell carcinoma ; Biopsy ; Carcinoma, Merkel Cell - pathology ; Dermis ; Differential diagnosis ; divergent differentiation ; Geriatrics ; Head and neck ; Head and Neck Neoplasms - pathology ; Humans ; Keratosis ; Male ; Melanoma ; Merkel cell carcinoma in situ ; Middle Aged ; Neoplasia ; Paget's disease ; Skin ; Skin Neoplasms - pathology ; Squamous cell carcinoma ; Tumors</subject><ispartof>Journal of cutaneous pathology, 2017-08, Vol.44 (8), p.684-691</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-c3536-3ff2562656e2489c424529452715c9312062cbf3c312d9a44f81e660bdf085063</citedby><cites>FETCH-LOGICAL-c3536-3ff2562656e2489c424529452715c9312062cbf3c312d9a44f81e660bdf085063</cites><orcidid>0000-0001-8916-8966</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcup.12966$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcup.12966$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28543532$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jour, George</creatorcontrib><creatorcontrib>Aung, Phyu P.</creatorcontrib><creatorcontrib>Rozas‐Muñoz, Eduardo</creatorcontrib><creatorcontrib>Curry, Johnathan L.</creatorcontrib><creatorcontrib>Prieto, Victor</creatorcontrib><creatorcontrib>Ivan, Doina</creatorcontrib><title>Intraepidermal Merkel cell carcinoma: A case series of a rare entity with clinical follow up</title><title>Journal of cutaneous pathology</title><addtitle>J Cutan Pathol</addtitle><description>Background
Merkel cell carcinoma (MCC) is a rare but aggressive cutaneous carcinoma. MCC typically involves dermis and although epidermotropism has been reported, MCC strictly intraepidermal or in situ (MCCIS) is exceedingly rare. Most of the cases of MCCIS described so far have other associated lesions, such as squamous or basal cell carcinoma, actinic keratosis and so on. Herein, we describe 3 patients with MCC strictly in situ, without a dermal component.
Methods
Our patients were elderly. 2 of the lesions involved the head and neck area and 1 was on a finger. All tumors were strictly intraepidermal in the diagnostic biopsies, and had histomorphologic features and an immunohistochemical profile supporting the diagnosis of MCC. Excisional biopsies were performed in 2 cases and failed to reveal dermal involvement by MCC or other associated malignancies.
Results and Conclusion
Our findings raise the awareness that MCC strictly in situ does exist and it should be included in the differential diagnosis of Paget's or extramammary Paget's disease, pagetoid squamous cell carcinoma, melanoma and other neoplasms that typically show histologically pagetoid extension of neoplastic cells. Considering the limited number of cases reported to date, the diagnosis of isolated MCCIS should not warrant a change in management from the typical MCC.</description><subject>Aged</subject><subject>Basal cell carcinoma</subject><subject>Biopsy</subject><subject>Carcinoma, Merkel Cell - pathology</subject><subject>Dermis</subject><subject>Differential diagnosis</subject><subject>divergent differentiation</subject><subject>Geriatrics</subject><subject>Head and neck</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>Humans</subject><subject>Keratosis</subject><subject>Male</subject><subject>Melanoma</subject><subject>Merkel cell carcinoma in situ</subject><subject>Middle Aged</subject><subject>Neoplasia</subject><subject>Paget's disease</subject><subject>Skin</subject><subject>Skin Neoplasms - pathology</subject><subject>Squamous cell carcinoma</subject><subject>Tumors</subject><issn>0303-6987</issn><issn>1600-0560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtLAzEQx4MoWh8Hv4AEvOhh2zw2011vpfiCih70JixpOsHUfZnsUvrtTa16EAxMZgI_fkz-hJxyNuTxjEzfDrnIAXbIgANjCVPAdsmASSYTyLPxATkMYckYhwzUPjkQmUqlkmJAXu_rzmts3QJ9pUv6gP4dS2qwjJf2xtVNpa_oJD4C0oDeYaCNpZp67ZFi3bluTVeue6OmdLUz0WGbsmxWtG-PyZ7VZcCT735EXm6un6d3yezx9n46mSUmLgGJtFYoEKAARZrlJhWpEnmsMVcml1wwEGZupYnjItdpajOOAGy-sCxTDOQRudh6W9989Bi6onJh8wVdY9OHgudMcoBMjSN6_gddNr2v43aREjymB6AidbmljG9C8GiL1rtK-3XBWbGJvIiRF1-RR_bs29jPK1z8kj8ZR2C0BVauxPX_pmL68rRVfgKx_4gE</recordid><startdate>201708</startdate><enddate>201708</enddate><creator>Jour, George</creator><creator>Aung, Phyu P.</creator><creator>Rozas‐Muñoz, Eduardo</creator><creator>Curry, Johnathan L.</creator><creator>Prieto, Victor</creator><creator>Ivan, Doina</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><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8916-8966</orcidid></search><sort><creationdate>201708</creationdate><title>Intraepidermal Merkel cell carcinoma: A case series of a rare entity with clinical follow up</title><author>Jour, George ; Aung, Phyu P. ; Rozas‐Muñoz, Eduardo ; Curry, Johnathan L. ; Prieto, Victor ; Ivan, Doina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-3ff2562656e2489c424529452715c9312062cbf3c312d9a44f81e660bdf085063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Basal cell carcinoma</topic><topic>Biopsy</topic><topic>Carcinoma, Merkel Cell - pathology</topic><topic>Dermis</topic><topic>Differential diagnosis</topic><topic>divergent differentiation</topic><topic>Geriatrics</topic><topic>Head and neck</topic><topic>Head and Neck Neoplasms - pathology</topic><topic>Humans</topic><topic>Keratosis</topic><topic>Male</topic><topic>Melanoma</topic><topic>Merkel cell carcinoma in situ</topic><topic>Middle Aged</topic><topic>Neoplasia</topic><topic>Paget's disease</topic><topic>Skin</topic><topic>Skin Neoplasms - pathology</topic><topic>Squamous cell carcinoma</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jour, George</creatorcontrib><creatorcontrib>Aung, Phyu P.</creatorcontrib><creatorcontrib>Rozas‐Muñoz, Eduardo</creatorcontrib><creatorcontrib>Curry, Johnathan L.</creatorcontrib><creatorcontrib>Prieto, Victor</creatorcontrib><creatorcontrib>Ivan, Doina</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><collection>MEDLINE - Academic</collection><jtitle>Journal of cutaneous pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jour, George</au><au>Aung, Phyu P.</au><au>Rozas‐Muñoz, Eduardo</au><au>Curry, Johnathan L.</au><au>Prieto, Victor</au><au>Ivan, Doina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intraepidermal Merkel cell carcinoma: A case series of a rare entity with clinical follow up</atitle><jtitle>Journal of cutaneous pathology</jtitle><addtitle>J Cutan Pathol</addtitle><date>2017-08</date><risdate>2017</risdate><volume>44</volume><issue>8</issue><spage>684</spage><epage>691</epage><pages>684-691</pages><issn>0303-6987</issn><eissn>1600-0560</eissn><abstract>Background
Merkel cell carcinoma (MCC) is a rare but aggressive cutaneous carcinoma. MCC typically involves dermis and although epidermotropism has been reported, MCC strictly intraepidermal or in situ (MCCIS) is exceedingly rare. Most of the cases of MCCIS described so far have other associated lesions, such as squamous or basal cell carcinoma, actinic keratosis and so on. Herein, we describe 3 patients with MCC strictly in situ, without a dermal component.
Methods
Our patients were elderly. 2 of the lesions involved the head and neck area and 1 was on a finger. All tumors were strictly intraepidermal in the diagnostic biopsies, and had histomorphologic features and an immunohistochemical profile supporting the diagnosis of MCC. Excisional biopsies were performed in 2 cases and failed to reveal dermal involvement by MCC or other associated malignancies.
Results and Conclusion
Our findings raise the awareness that MCC strictly in situ does exist and it should be included in the differential diagnosis of Paget's or extramammary Paget's disease, pagetoid squamous cell carcinoma, melanoma and other neoplasms that typically show histologically pagetoid extension of neoplastic cells. Considering the limited number of cases reported to date, the diagnosis of isolated MCCIS should not warrant a change in management from the typical MCC.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>28543532</pmid><doi>10.1111/cup.12966</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-8916-8966</orcidid></addata></record> |
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subjects | Aged Basal cell carcinoma Biopsy Carcinoma, Merkel Cell - pathology Dermis Differential diagnosis divergent differentiation Geriatrics Head and neck Head and Neck Neoplasms - pathology Humans Keratosis Male Melanoma Merkel cell carcinoma in situ Middle Aged Neoplasia Paget's disease Skin Skin Neoplasms - pathology Squamous cell carcinoma Tumors |
title | Intraepidermal Merkel cell carcinoma: A case series of a rare entity with clinical follow up |
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