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.


ABOUT ARCHIVES
Advanced Search

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


  Vol. 133 No. 6, June 1997 TABLE OF CONTENTS
  Archives
  •  Online Features
  OBSERVATIONS
 This Article
 •References
 •Full text PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on Web of Science (6)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Palpable Migratory Arciform Erythema

Clinical Morphology, Histopathology, Immunohistochemistry, and Response to Treatment

Dietrich Abeck, MD; Markus W. Ollert, MD; Fritjof Eckert, MD; Rolf-Markus Szeimies, MD; Markus Tiemann, MD; Otto Braun-Falco, MD; Volker Steinkraus, MD; Johannes Ring, MD, PhD

Arch Dermatol. 1997;133(6):763-766.


Abstract

Background
Palpable migratory arciform erythema is clinically characterized by sharply circumscribed, infiltrated erythematous patches that tend to spread irregularly, resulting in arciform morphologic features. The histopathologic features are characterized by a patchy inflammatory perivascular and periadnexal T-lym-phocytic infiltrate throughout the dermis. The disease runs a chronic course and is rarely described in the literature.

Observation
Three middle-aged patients of both sexes had palpable migratory arciform erythema with 1, several, or multiple lesions on the trunk. There was a dense perivascular and periadnexal, predominantly lymphocytic infiltrate of the reticular dermis without any interstitial distribution of inflammatory cells. Absence of mucin deposits and plasma cells was a striking feature. The immunohistochemical profile showed an infiltrate dominated by T cells of polyclonal origin. In addition, polyclonal B cells and histiocytes were present in small numbers. In all 3 cases, oral antibacterial treatment resulted in a complete (2 patients) or temporary (1 patient) resolution of skin lesions.

Conclusions
Palpable migratory arciform erythema shows distinctive differences in clinical and pathological features and treatment in contrast to other diseases with cutaneous lymphocytic infiltrates, including lymphocytic infiltration of Jessner and Kanof. Therefore, it is likely a distinct disease entity.

Arch Dermatol. 1997;133:763-766



Author Affiliations

From the Departments of Dermatology, Universität-Krankenhaus Eppendorf, Hamburg, Germany (Drs Abeck, Steinkraus, and Ring) and Ludwig-Maximilians-Universität, Munich, Germany (Drs Ollert, Eckert, Szeimies, and Braun-Falco), and the Institute of Hematopathology, Kiel, Germany (Dr Tiemann).



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Coincidential successful treatment of Jessner-Kanof disease with chemotherapy
Ardavanis et al.
Ann Oncol 2008;19:1360-1361.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1997 American Medical Association. All Rights Reserved.