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Cancer and hidradenitis suppurativa
Patients with hidradenitis suppurativa (HS) have an increased risk of developing cancer. This includes not only hematologic malignancies and solid tumors but also cutaneous squamous cell carcinoma (SCC) originating within the HS lesions. The development of SCC is most commonly associated with Caucas...
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Published in: | Clinics in dermatology 2024-11, Vol.42 (6), p.585-601 |
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description | Patients with hidradenitis suppurativa (HS) have an increased risk of developing cancer. This includes not only hematologic malignancies and solid tumors but also cutaneous squamous cell carcinoma (SCC) originating within the HS lesions. The development of SCC is most commonly associated with Caucasian men who smoke and have severe gluteal or perianal lesions of more than 25 years. Other factors that have occasionally been associated with HS-related SCC include treatment with a tumor necrosis factor-alpha inhibitor (such as infliximab and adalimumab), genodermatoses (such as keratitis-ichthyosis-deafness syndrome and Dowling-Degos disease), and paraneoplastic syndromes (such as hypercalcemia, hypercalcemia-leukocytosis, and paraneoplastic neuropathy). The tumor may demonstrate the presence of human papillomavirus; even after treatment, patients have a poor prognosis because cancer metastasis, recurrence, or both commonly occur. The potential role of human papillomavirus vaccination for cancer prevention and early treatment of SCC with targeted therapy (with an epidermal growth factor inhibitor such as cetuximab) and/or checkpoint inhibitor immunotherapy (such as cemiplimab and pembrolizumab) remains to be determined. Rarely, HS lesions have mimicked cutaneous metastases in patients with visceral malignancy by demonstrating an increased uptake of fluorine-18 fluorodeoxyglucose on positron emission tomography and/or computed tomography scans. Primary cancers (such as cutaneous SCC and mucinous adenocarcinoma) and breast cancer skin metastases can masquerade as HS lesions. When a lesion is located at a current or earlier site of HS that is new or rapidly growing and/or does not respond to HS-directed therapy, prompt evaluation to establish or exclude the diagnosis of cancer should be considered. |
doi_str_mv | 10.1016/j.clindermatol.2024.09.014 |
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This includes not only hematologic malignancies and solid tumors but also cutaneous squamous cell carcinoma (SCC) originating within the HS lesions. The development of SCC is most commonly associated with Caucasian men who smoke and have severe gluteal or perianal lesions of more than 25 years. Other factors that have occasionally been associated with HS-related SCC include treatment with a tumor necrosis factor-alpha inhibitor (such as infliximab and adalimumab), genodermatoses (such as keratitis-ichthyosis-deafness syndrome and Dowling-Degos disease), and paraneoplastic syndromes (such as hypercalcemia, hypercalcemia-leukocytosis, and paraneoplastic neuropathy). The tumor may demonstrate the presence of human papillomavirus; even after treatment, patients have a poor prognosis because cancer metastasis, recurrence, or both commonly occur. The potential role of human papillomavirus vaccination for cancer prevention and early treatment of SCC with targeted therapy (with an epidermal growth factor inhibitor such as cetuximab) and/or checkpoint inhibitor immunotherapy (such as cemiplimab and pembrolizumab) remains to be determined. Rarely, HS lesions have mimicked cutaneous metastases in patients with visceral malignancy by demonstrating an increased uptake of fluorine-18 fluorodeoxyglucose on positron emission tomography and/or computed tomography scans. Primary cancers (such as cutaneous SCC and mucinous adenocarcinoma) and breast cancer skin metastases can masquerade as HS lesions. When a lesion is located at a current or earlier site of HS that is new or rapidly growing and/or does not respond to HS-directed therapy, prompt evaluation to establish or exclude the diagnosis of cancer should be considered.</description><identifier>ISSN: 0738-081X</identifier><identifier>ISSN: 1879-1131</identifier><identifier>EISSN: 1879-1131</identifier><identifier>DOI: 10.1016/j.clindermatol.2024.09.014</identifier><identifier>PMID: 39260459</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Carcinoma, Squamous Cell - diagnosis ; Carcinoma, Squamous Cell - etiology ; Carcinoma, Squamous Cell - therapy ; Female ; Hidradenitis Suppurativa - complications ; Hidradenitis Suppurativa - therapy ; Humans ; Male ; Papillomavirus Infections - complications ; Paraneoplastic Syndromes - diagnosis ; Paraneoplastic Syndromes - etiology ; Risk Factors ; Skin Neoplasms - diagnosis ; Skin Neoplasms - therapy</subject><ispartof>Clinics in dermatology, 2024-11, Vol.42 (6), p.585-601</ispartof><rights>2024 The Author(s)</rights><rights>Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2204-686f654ec07fcb3e2dffcb67143c088d831de6545d24d817c06697d62c69ff713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39260459$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cohen, Philip R.</creatorcontrib><creatorcontrib>Cohen-Kurzrock, Rena A.</creatorcontrib><creatorcontrib>Riahi, Ryan R.</creatorcontrib><title>Cancer and hidradenitis suppurativa</title><title>Clinics in dermatology</title><addtitle>Clin Dermatol</addtitle><description>Patients with hidradenitis suppurativa (HS) have an increased risk of developing cancer. This includes not only hematologic malignancies and solid tumors but also cutaneous squamous cell carcinoma (SCC) originating within the HS lesions. The development of SCC is most commonly associated with Caucasian men who smoke and have severe gluteal or perianal lesions of more than 25 years. Other factors that have occasionally been associated with HS-related SCC include treatment with a tumor necrosis factor-alpha inhibitor (such as infliximab and adalimumab), genodermatoses (such as keratitis-ichthyosis-deafness syndrome and Dowling-Degos disease), and paraneoplastic syndromes (such as hypercalcemia, hypercalcemia-leukocytosis, and paraneoplastic neuropathy). The tumor may demonstrate the presence of human papillomavirus; even after treatment, patients have a poor prognosis because cancer metastasis, recurrence, or both commonly occur. The potential role of human papillomavirus vaccination for cancer prevention and early treatment of SCC with targeted therapy (with an epidermal growth factor inhibitor such as cetuximab) and/or checkpoint inhibitor immunotherapy (such as cemiplimab and pembrolizumab) remains to be determined. Rarely, HS lesions have mimicked cutaneous metastases in patients with visceral malignancy by demonstrating an increased uptake of fluorine-18 fluorodeoxyglucose on positron emission tomography and/or computed tomography scans. Primary cancers (such as cutaneous SCC and mucinous adenocarcinoma) and breast cancer skin metastases can masquerade as HS lesions. When a lesion is located at a current or earlier site of HS that is new or rapidly growing and/or does not respond to HS-directed therapy, prompt evaluation to establish or exclude the diagnosis of cancer should be considered.</description><subject>Carcinoma, Squamous Cell - diagnosis</subject><subject>Carcinoma, Squamous Cell - etiology</subject><subject>Carcinoma, Squamous Cell - therapy</subject><subject>Female</subject><subject>Hidradenitis Suppurativa - complications</subject><subject>Hidradenitis Suppurativa - therapy</subject><subject>Humans</subject><subject>Male</subject><subject>Papillomavirus Infections - complications</subject><subject>Paraneoplastic Syndromes - diagnosis</subject><subject>Paraneoplastic Syndromes - etiology</subject><subject>Risk Factors</subject><subject>Skin Neoplasms - diagnosis</subject><subject>Skin Neoplasms - therapy</subject><issn>0738-081X</issn><issn>1879-1131</issn><issn>1879-1131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqNkEtLAzEUhYMotlb_ghTduJnxZpImGXdSn1Bwo-AupMkdTJlHTWYK_ntTWsWlq7P5zj3cj5ALCjkFKq5Xua196zA0pu_qvICC51DmQPkBGVMly4xSRg_JGCRTGSj6PiInMa4AgIOAYzJiZSGAz8oxuZyb1mKYmtZNP7wLxmHrex-ncVivh2B6vzGn5KgydcSzfU7I28P96_wpW7w8Ps9vF5ktCuCZUKISM44WZGWXDAtXpRSScmZBKacYdZiAmSu4U1RaEKKUThRWlFUlKZuQq93ddeg-B4y9bny0WNemxW6ImlFgnHMlZUJvdqgNXYwBK70OvjHhS1PQW0l6pf9K0ltJGkqdJKXy-X5nWDbofqs_VhJwtwMwfbvxGHS0HpMn5wPaXrvO_2fnG14Vfgc</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Cohen, Philip R.</creator><creator>Cohen-Kurzrock, Rena A.</creator><creator>Riahi, Ryan R.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><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></search><sort><creationdate>202411</creationdate><title>Cancer and hidradenitis suppurativa</title><author>Cohen, Philip R. ; Cohen-Kurzrock, Rena A. ; Riahi, Ryan R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2204-686f654ec07fcb3e2dffcb67143c088d831de6545d24d817c06697d62c69ff713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Carcinoma, Squamous Cell - diagnosis</topic><topic>Carcinoma, Squamous Cell - etiology</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>Female</topic><topic>Hidradenitis Suppurativa - complications</topic><topic>Hidradenitis Suppurativa - therapy</topic><topic>Humans</topic><topic>Male</topic><topic>Papillomavirus Infections - complications</topic><topic>Paraneoplastic Syndromes - diagnosis</topic><topic>Paraneoplastic Syndromes - etiology</topic><topic>Risk Factors</topic><topic>Skin Neoplasms - diagnosis</topic><topic>Skin Neoplasms - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cohen, Philip R.</creatorcontrib><creatorcontrib>Cohen-Kurzrock, Rena A.</creatorcontrib><creatorcontrib>Riahi, Ryan R.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><jtitle>Clinics in dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cohen, Philip R.</au><au>Cohen-Kurzrock, Rena A.</au><au>Riahi, Ryan R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cancer and hidradenitis suppurativa</atitle><jtitle>Clinics in dermatology</jtitle><addtitle>Clin Dermatol</addtitle><date>2024-11</date><risdate>2024</risdate><volume>42</volume><issue>6</issue><spage>585</spage><epage>601</epage><pages>585-601</pages><issn>0738-081X</issn><issn>1879-1131</issn><eissn>1879-1131</eissn><abstract>Patients with hidradenitis suppurativa (HS) have an increased risk of developing cancer. This includes not only hematologic malignancies and solid tumors but also cutaneous squamous cell carcinoma (SCC) originating within the HS lesions. The development of SCC is most commonly associated with Caucasian men who smoke and have severe gluteal or perianal lesions of more than 25 years. Other factors that have occasionally been associated with HS-related SCC include treatment with a tumor necrosis factor-alpha inhibitor (such as infliximab and adalimumab), genodermatoses (such as keratitis-ichthyosis-deafness syndrome and Dowling-Degos disease), and paraneoplastic syndromes (such as hypercalcemia, hypercalcemia-leukocytosis, and paraneoplastic neuropathy). The tumor may demonstrate the presence of human papillomavirus; even after treatment, patients have a poor prognosis because cancer metastasis, recurrence, or both commonly occur. The potential role of human papillomavirus vaccination for cancer prevention and early treatment of SCC with targeted therapy (with an epidermal growth factor inhibitor such as cetuximab) and/or checkpoint inhibitor immunotherapy (such as cemiplimab and pembrolizumab) remains to be determined. Rarely, HS lesions have mimicked cutaneous metastases in patients with visceral malignancy by demonstrating an increased uptake of fluorine-18 fluorodeoxyglucose on positron emission tomography and/or computed tomography scans. Primary cancers (such as cutaneous SCC and mucinous adenocarcinoma) and breast cancer skin metastases can masquerade as HS lesions. 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subjects | Carcinoma, Squamous Cell - diagnosis Carcinoma, Squamous Cell - etiology Carcinoma, Squamous Cell - therapy Female Hidradenitis Suppurativa - complications Hidradenitis Suppurativa - therapy Humans Male Papillomavirus Infections - complications Paraneoplastic Syndromes - diagnosis Paraneoplastic Syndromes - etiology Risk Factors Skin Neoplasms - diagnosis Skin Neoplasms - therapy |
title | Cancer and hidradenitis suppurativa |
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