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The Cutaneous Manifestations of the Functioning Carcinoid
ROBERT R. KIERLAND, M.D.;
WILLIAM G. SAUER, M.D.;
WILLIAM H. DEARING, M.D.
AMA Arch Derm. 1958;77(1):86-90.
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The purpose of this communication is not to review the extensive literature that has appeared concerning this recently recognized syndrome of functioning carcinoid but to review for dermatologists the salient clinical features, especially the cutaneous ones, that may lead to recognition and diagnosis.
Since 1952 and 1953, when four independent reports1-4 appeared concerning a new syndrome, many additional reports of cases, experimental work, and the pathogenesis of this previously unidentified symptom complex, called the "functioning carcinoid" or the "carcinoid syndrome," have been published.5-7 The original reports were actually the outcome of much previous work by physiologists and others concerning the physiology of serotonin and enteramine, which were both subsequently shown to be 5-hydroxytryptamine.5-7 Lembeck8 first demonstrated that carcinoid tumors may contain large amounts of 5-hydroxytryptamine. It is the liberation of 5-hydroxytryptamine into the blood stream by the cells of
. . . [Full Text PDF of this Article]
Author Affiliations
Rochester, Minn.
Footnotes
Received for publication Sept. 6, 1957.
Read before the 77th Annual Meeting of the American Dermatological Association, Inc., Belleair, Fla., April 15, 1957. The presentation included a colored motion picture.
Section of Dermatology (Dr. Kierland) and Section of Medicine (Drs. Sauer and Dearing), Mayo Clinic and Mayo Foundation. The Mayo Foundation, Rochester, Minn., is a part of the Graduate School of the University of Minnesota.
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