You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


Advertisement

ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | RSS | Access Rights | Sign In


  Vol. 145 No. 8, August 2009 TABLE OF CONTENTS
  Online Only
 •  Online First Table of
Contents
  Editorial
 •Online Features
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on Web of Science (1)
 •Contact me when this article is cited
 Related Content
 •Related article
 •Similar articles in this journal
 Topic Collections
 •Neurology
 •Neuromuscular diseases
 •Dermatology
 •Dermatologic Disorders
 •Pediatrics
 •Pediatrics, Other
 •Diagnosis
 •Dermatologic Disorders, Other
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Delicious Add to Digg Add to Facebook Add to Reddit Add to Technorati Add to Twitter What's this?

Diagnostic and Management Considerations Posed by Multiple Café au Lait Spots

Vincent M. Riccardi, MD

Arch Dermatol. 2009;145(8):929-930.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Neurofibromatosis type 1 (NF1) is potentially a very serious disease. A cardinal feature of NF1 is the patchy hyperpigmentation of the skin variously known as café au lait macules (CALMs) or café au lait spots (CLSs). In this issue of the Archives, Nunley and coworkers1 document unequivocally that 6 or more CLSs, as the sole clinical finding, are especially useful for alerting clinicians to the ultimate diagnosis of NF1. That is, as the title of their article indicates, CLSs can be predictive of the diagnosis of NF1. The purpose of this editorial is to emphasize this conclusion and to discuss 2 further considerations: (1) NF1 CLSs in no way predict the nature and severity of the disorder once it fully manifests; and (2) CLSs overlapping in nature, number, and distribution with NF1 may indicate an alternative disorder. That is, clinicians must deal with both the . . . [Full Text of this Article]

TYPICAL AND ATYPICAL CLSs


NEUROIMAGING STUDIES AND MOLECULAR DNA MUTATION ANALYSIS

AUTHOR INFORMATION


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Delicious Delicious   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

RELATED ARTICLE

Predictive Value of Café au Lait Macules at Initial Consultation in the Diagnosis of Neurofibromatosis Type 1
Kara S. Nunley, Feng Gao, Anne C. Albers, Susan J. Bayliss, and David H. Gutmann
Arch Dermatol. 2009;145(8):883-887.
ABSTRACT | FULL TEXT  






HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | PHYSICIAN JOBS | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2009 American Medical Association. All Rights Reserved.