The New England Journal of Medicine
e-mail icon  FREE NEJM E-TOC    HOME   |   SUBSCRIBE   |   CURRENT ISSUE   |   PAST ISSUES   |   COLLECTIONS   |    Advanced Search
Sign in | Get NEJM's E-Mail Table of Contents — Free | Subscribe
 
Original Article
Brief Report
PreviousPrevious
Volume 339:883-886 September 24, 1998 Number 13
NextNext

Cushing's Syndrome Caused by Corticotropin Secretion by Pulmonary Tumorlets
Elif Arioglu, M.D., John Doppman, M.D., Mario Gomes, M.D., David Kleiner, M.D., Ph.D., David Mauro, M.D., Ph.D., Carolee Barlow, M.D., Ph.D., and Dimitris A. Papanicolaou, M.D.

Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

 Sign up for free e-toc
 

This Article
-Full Text
- PDF

Tools and Services
-Add to Personal Archive
-Add to Citation Manager
-Notify a Friend
-E-mail When Cited

More Information
-PubMed Citation
The term "pulmonary tumorlets" describes multiple microscopic nests of neuroendocrine cells in the lungs.1 Like bronchial carcinoid tumors and small-cell carcinomas, pulmonary tumorlets arise from Kulchitsky's cells. In the lung the abnormalities in these cells range from hyperplasia to malignant transformation, since control over cellular growth is lost.2

Both bronchial carcinoid tumors and small-cell lung carcinomas may secrete corticotropin in sufficient quantities to cause Cushing's syndrome. We describe a patient with Cushing's syndrome due to ectopic secretion of corticotropin in whom the source of the excess corticotropin was ultimately found to be hundreds of tumorlets in one lobe of the . . . [Full Text of this Article]

Case Report

Discussion


Source Information

From the Diabetes Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Md. (E.A.); the Department of Radiology, Clinical Center, National Institutes of Health, Bethesda, Md. (J.D.); the Department of Thoracic and Cardiovascular Surgery, Georgetown University Hospital, Washington, D.C. (M.G.); the Department of Pathology, National Cancer Institute, Bethesda, Md. (D.K., D.M.); the National Human Genome Research Institute, Laboratory of Genetic Disease Research and the National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Md. (C.B.); and the Developmental Endocrinology Branch, National Institute of Child Health and Human Development, Bethesda, Md. (D.A.P.).

Address reprint requests to Dr. Papanicolaou at the Developmental Endocrinology Branch, National Institute of Child Health and Human Development, Bldg. 10, Rm. 10N262, 10 Center Dr. MSC 1862, Bethesda, MD 20892-1862.

References


This article has been cited by other articles:



HOME  |  SUBSCRIBE  |  SEARCH  |  CURRENT ISSUE  |  PAST ISSUES  |  COLLECTIONS  |  PRIVACY  |  TERMS OF USE  |  HELP  |  beta.nejm.org

Comments and questions? Please contact us.

The New England Journal of Medicine is owned, published, and copyrighted © 2009 Massachusetts Medical Society. All rights reserved.