Cutaneous manifestations of the malignant carcinoid syndrome
Summary Background The incidence of carcinoid tumours is approximately 1·5 per 100 000 of the population. The malignant carcinoid syndrome, which is caused by circulating neuroendocrine mediators produced by the tumour, occurs in less than 10% of patients. Cutaneous involvement, although recognized...
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Veröffentlicht in: | British journal of dermatology (1951) 2005-01, Vol.152 (1), p.71-75 |
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creator | Bell, H.K. Poston, G.J. Vora, J. Wilson, N.J.E. |
description | Summary
Background The incidence of carcinoid tumours is approximately 1·5 per 100 000 of the population. The malignant carcinoid syndrome, which is caused by circulating neuroendocrine mediators produced by the tumour, occurs in less than 10% of patients. Cutaneous involvement, although recognized in this rare syndrome, has rarely been reported.
Objectives To examine a series of patients with the malignant carcinoid syndrome, to establish the prevalence and types of cutaneous involvement and to assess whether these could be used as indicators of disease activity, progression and prognosis.
Methods Patients with the malignant carcinoid syndrome who attended a multidisciplinary clinic for neuroendocrine tumours over a 23‐month period between February 2001 and December 2002 were invited to participate in the study. This involved completion of a standard history proforma and a detailed cutaneous examination with findings recorded by clinical photography.
Results Twenty‐five patients were enrolled. All but one had experienced flushing, three had rosacea, five had clinical features of pellagra and two had scleroderma. Flushing was generally an early manifestation of the syndrome, whereas both the pellagra and scleroderma tended to occur in more advanced disease.
Conclusions This descriptive case series indicates that cutaneous features are not uncommon in the syndrome. They are readily diagnosed on clinical examination, and may be useful indicators of disease activity and prognosis. |
doi_str_mv | 10.1111/j.1365-2133.2004.06273.x |
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Background The incidence of carcinoid tumours is approximately 1·5 per 100 000 of the population. The malignant carcinoid syndrome, which is caused by circulating neuroendocrine mediators produced by the tumour, occurs in less than 10% of patients. Cutaneous involvement, although recognized in this rare syndrome, has rarely been reported.
Objectives To examine a series of patients with the malignant carcinoid syndrome, to establish the prevalence and types of cutaneous involvement and to assess whether these could be used as indicators of disease activity, progression and prognosis.
Methods Patients with the malignant carcinoid syndrome who attended a multidisciplinary clinic for neuroendocrine tumours over a 23‐month period between February 2001 and December 2002 were invited to participate in the study. This involved completion of a standard history proforma and a detailed cutaneous examination with findings recorded by clinical photography.
Results Twenty‐five patients were enrolled. All but one had experienced flushing, three had rosacea, five had clinical features of pellagra and two had scleroderma. Flushing was generally an early manifestation of the syndrome, whereas both the pellagra and scleroderma tended to occur in more advanced disease.
Conclusions This descriptive case series indicates that cutaneous features are not uncommon in the syndrome. They are readily diagnosed on clinical examination, and may be useful indicators of disease activity and prognosis.</description><identifier>ISSN: 0007-0963</identifier><identifier>EISSN: 1365-2133</identifier><identifier>DOI: 10.1111/j.1365-2133.2004.06273.x</identifier><identifier>PMID: 15656803</identifier><identifier>CODEN: BJDEAZ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; carcinoid ; Carcinoid Tumor - secondary ; cutaneous ; Dermatology ; Disease Progression ; Facial Dermatoses - diagnosis ; Female ; flushing ; Flushing - diagnosis ; Humans ; Liver Neoplasms - secondary ; Male ; Malignant Carcinoid Syndrome - diagnosis ; Malignant Carcinoid Syndrome - pathology ; Medical sciences ; Middle Aged ; pellagra ; Prognosis ; Rosacea - diagnosis ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; scleroderma ; Scleroderma, Systemic - diagnosis ; Skin Diseases - diagnosis ; Skin Diseases - pathology ; Skin involvement in other diseases. Miscellaneous. General aspects ; Skin Neoplasms - diagnosis ; Skin Neoplasms - secondary ; Vascular disorders of the skin</subject><ispartof>British journal of dermatology (1951), 2005-01, Vol.152 (1), p.71-75</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Blackwell Publishing Jan 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4623-531e081df58d7262954e5ec784fcaac6de029b8fc6255364db6dcad7bea479913</citedby><cites>FETCH-LOGICAL-c4623-531e081df58d7262954e5ec784fcaac6de029b8fc6255364db6dcad7bea479913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2133.2004.06273.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2133.2004.06273.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27900,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17104945$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15656803$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bell, H.K.</creatorcontrib><creatorcontrib>Poston, G.J.</creatorcontrib><creatorcontrib>Vora, J.</creatorcontrib><creatorcontrib>Wilson, N.J.E.</creatorcontrib><title>Cutaneous manifestations of the malignant carcinoid syndrome</title><title>British journal of dermatology (1951)</title><addtitle>Br J Dermatol</addtitle><description>Summary
Background The incidence of carcinoid tumours is approximately 1·5 per 100 000 of the population. The malignant carcinoid syndrome, which is caused by circulating neuroendocrine mediators produced by the tumour, occurs in less than 10% of patients. Cutaneous involvement, although recognized in this rare syndrome, has rarely been reported.
Objectives To examine a series of patients with the malignant carcinoid syndrome, to establish the prevalence and types of cutaneous involvement and to assess whether these could be used as indicators of disease activity, progression and prognosis.
Methods Patients with the malignant carcinoid syndrome who attended a multidisciplinary clinic for neuroendocrine tumours over a 23‐month period between February 2001 and December 2002 were invited to participate in the study. This involved completion of a standard history proforma and a detailed cutaneous examination with findings recorded by clinical photography.
Results Twenty‐five patients were enrolled. All but one had experienced flushing, three had rosacea, five had clinical features of pellagra and two had scleroderma. Flushing was generally an early manifestation of the syndrome, whereas both the pellagra and scleroderma tended to occur in more advanced disease.
Conclusions This descriptive case series indicates that cutaneous features are not uncommon in the syndrome. They are readily diagnosed on clinical examination, and may be useful indicators of disease activity and prognosis.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>carcinoid</subject><subject>Carcinoid Tumor - secondary</subject><subject>cutaneous</subject><subject>Dermatology</subject><subject>Disease Progression</subject><subject>Facial Dermatoses - diagnosis</subject><subject>Female</subject><subject>flushing</subject><subject>Flushing - diagnosis</subject><subject>Humans</subject><subject>Liver Neoplasms - secondary</subject><subject>Male</subject><subject>Malignant Carcinoid Syndrome - diagnosis</subject><subject>Malignant Carcinoid Syndrome - pathology</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>pellagra</subject><subject>Prognosis</subject><subject>Rosacea - diagnosis</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>scleroderma</subject><subject>Scleroderma, Systemic - diagnosis</subject><subject>Skin Diseases - diagnosis</subject><subject>Skin Diseases - pathology</subject><subject>Skin involvement in other diseases. Miscellaneous. General aspects</subject><subject>Skin Neoplasms - diagnosis</subject><subject>Skin Neoplasms - secondary</subject><subject>Vascular disorders of the skin</subject><issn>0007-0963</issn><issn>1365-2133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkM2O0zAURi0EYsrAK6AICXYJ1_-JBAtomRY0gg2IpeXaDrgkzmAnon17nEk1I7HCG1v2OVefP4QKDBXO6_WhwlTwkmBKKwLAKhBE0ur4AK3uHh6iFQDIEhpBL9CTlA4AmAKHx-gCc8FFDXSF3qynUQc3TKnodfCtS6Me_RBSMbTF-NPl287_CDqMhdHR-DB4W6RTsHHo3VP0qNVdcs_O-yX6dvXh63pXXn_Zfly_uy4NE4SWnGIHNbYtr60kgjScOe6MrFlrtDbCOiDNvm6NIJxTwexeWKOt3DvNZNNgeoleLXNv4vB7yhFV75NxXbckV0JS2RBOM_jiH_AwTDHkbIrMv6cNhwzVC2TikFJ0rbqJvtfxpDCouV51UHOLam5x9pi6rVcds_r8PH_a987ei-c-M_DyDOhkdNdGHYxP95zEwBrGM_d24f74zp3-O4B6_2kzn7JfLr5Pozve-Tr-ui2Dq--ft-pqS3ab3WardvQvvEaj2Q</recordid><startdate>200501</startdate><enddate>200501</enddate><creator>Bell, H.K.</creator><creator>Poston, G.J.</creator><creator>Vora, J.</creator><creator>Wilson, N.J.E.</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>200501</creationdate><title>Cutaneous manifestations of the malignant carcinoid syndrome</title><author>Bell, H.K. ; Poston, G.J. ; Vora, J. ; Wilson, N.J.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4623-531e081df58d7262954e5ec784fcaac6de029b8fc6255364db6dcad7bea479913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>carcinoid</topic><topic>Carcinoid Tumor - secondary</topic><topic>cutaneous</topic><topic>Dermatology</topic><topic>Disease Progression</topic><topic>Facial Dermatoses - diagnosis</topic><topic>Female</topic><topic>flushing</topic><topic>Flushing - diagnosis</topic><topic>Humans</topic><topic>Liver Neoplasms - secondary</topic><topic>Male</topic><topic>Malignant Carcinoid Syndrome - diagnosis</topic><topic>Malignant Carcinoid Syndrome - pathology</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>pellagra</topic><topic>Prognosis</topic><topic>Rosacea - diagnosis</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>scleroderma</topic><topic>Scleroderma, Systemic - diagnosis</topic><topic>Skin Diseases - diagnosis</topic><topic>Skin Diseases - pathology</topic><topic>Skin involvement in other diseases. Miscellaneous. General aspects</topic><topic>Skin Neoplasms - diagnosis</topic><topic>Skin Neoplasms - secondary</topic><topic>Vascular disorders of the skin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bell, H.K.</creatorcontrib><creatorcontrib>Poston, G.J.</creatorcontrib><creatorcontrib>Vora, J.</creatorcontrib><creatorcontrib>Wilson, N.J.E.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of dermatology (1951)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bell, H.K.</au><au>Poston, G.J.</au><au>Vora, J.</au><au>Wilson, N.J.E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cutaneous manifestations of the malignant carcinoid syndrome</atitle><jtitle>British journal of dermatology (1951)</jtitle><addtitle>Br J Dermatol</addtitle><date>2005-01</date><risdate>2005</risdate><volume>152</volume><issue>1</issue><spage>71</spage><epage>75</epage><pages>71-75</pages><issn>0007-0963</issn><eissn>1365-2133</eissn><coden>BJDEAZ</coden><abstract>Summary
Background The incidence of carcinoid tumours is approximately 1·5 per 100 000 of the population. The malignant carcinoid syndrome, which is caused by circulating neuroendocrine mediators produced by the tumour, occurs in less than 10% of patients. Cutaneous involvement, although recognized in this rare syndrome, has rarely been reported.
Objectives To examine a series of patients with the malignant carcinoid syndrome, to establish the prevalence and types of cutaneous involvement and to assess whether these could be used as indicators of disease activity, progression and prognosis.
Methods Patients with the malignant carcinoid syndrome who attended a multidisciplinary clinic for neuroendocrine tumours over a 23‐month period between February 2001 and December 2002 were invited to participate in the study. This involved completion of a standard history proforma and a detailed cutaneous examination with findings recorded by clinical photography.
Results Twenty‐five patients were enrolled. All but one had experienced flushing, three had rosacea, five had clinical features of pellagra and two had scleroderma. Flushing was generally an early manifestation of the syndrome, whereas both the pellagra and scleroderma tended to occur in more advanced disease.
Conclusions This descriptive case series indicates that cutaneous features are not uncommon in the syndrome. They are readily diagnosed on clinical examination, and may be useful indicators of disease activity and prognosis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15656803</pmid><doi>10.1111/j.1365-2133.2004.06273.x</doi><tpages>5</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Biological and medical sciences carcinoid Carcinoid Tumor - secondary cutaneous Dermatology Disease Progression Facial Dermatoses - diagnosis Female flushing Flushing - diagnosis Humans Liver Neoplasms - secondary Male Malignant Carcinoid Syndrome - diagnosis Malignant Carcinoid Syndrome - pathology Medical sciences Middle Aged pellagra Prognosis Rosacea - diagnosis Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis scleroderma Scleroderma, Systemic - diagnosis Skin Diseases - diagnosis Skin Diseases - pathology Skin involvement in other diseases. Miscellaneous. General aspects Skin Neoplasms - diagnosis Skin Neoplasms - secondary Vascular disorders of the skin |
title | Cutaneous manifestations of the malignant carcinoid syndrome |
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