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
Hauptverfasser: Bell, H.K., Poston, G.J., Vora, J., Wilson, N.J.E.
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container_issue 1
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container_title British journal of dermatology (1951)
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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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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. 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Vasculitis ; scleroderma ; Scleroderma, Systemic - diagnosis ; Skin Diseases - diagnosis ; Skin Diseases - pathology ; Skin involvement in other diseases. Miscellaneous. 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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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; 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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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete
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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