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. 126 No. 1, January 1990 TABLE OF CONTENTS
  Archives
  •  Online Features
  EDITORIAL REVIEW
 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
 •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?

The Natural History of Vasculitis

What the Histology Tells Us About Pathogenesis

Bruce R. Smoller, MD; N. Scott McNutt, MD; Félix Contreras, MD

Arch Dermatol. 1990;126(1):84-89.


Abstract

• While histopathologic analysis may offer some clues as to the pathogenesis of vasculitis, observations must be interpreted with caution, as there is considerable overlap in the histologic pattern. In most cases, a predominantly neutrophilic vasculitis affecting small dermal venules suggests a relatively acute, immune complex-mediated reaction. Less commonly, this histologic pattern may be seen in non-immunologically mediated processes, such as in the presence of bacterial toxins or malignant hypertension, or in more chronic disease states, such as granuloma faciale or erythema elevatum diutinum. A predominantly lymphocytic vasculitis may represent several pathogenetic mechanisms. In lesions more than 24 to 48 hours old, a lymphocytic vasculitis may represent a resolving phase of an immune complex-mediated neutrophilic vasculitis. Alternatively, this histologic pattern may be seen de novo in conditions with a presumed cell-mediated immunologic pathogenesis. Lymphocytic vasculitis may also be seen in rickettsial infections such as Rocky Mountain spotted fever. The pathogenesis of granulomatous vasculitis remains poorly understood and is thought to be induced by a combination of circulating immune complexes and a cell-mediated immune response.

(Arch Dermatol. 1990;126:84-89)



Author Affiliations

From the Departments of Medicine (Dermatology) (Dr Smoller) and Pathology, Dermatopathology Division (Dr McNutt), New York Hospital-Cornell University Medical Center, New York, NY, and the Department of Pathology, La Paz Hospital Medical School, Madrid, Spain.


Footnotes

Accepted for publication August 17, 1989.

Reprint requests to Dermatopathology Division, F-309, Department of Pathology, New York Hospital, 525 E 68th St, New York, NY 10021 (Dr Smoller).



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

Leucocytoclastic vasculitis as onset symptom of ulcerative colitis
Iannone et al.
Ann Rheum Dis 2003;62:785-786.
FULL TEXT  

Clinical Manifestations of Vasculitis in Patients With Solid Tumors: A Case Report and Review of the Literature
Kurzrock et al.
Arch Intern Med 1994;154:334-340.
ABSTRACT  

Benign Cutaneous Polyarteritis Nodosa: Relationship to Systemic Polyarteritis Nodosa and to Hepatitis B Infection
Minkowitz et al.
Arch Dermatol 1991;127:1520-1523.
ABSTRACT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1990 American Medical Association. All Rights Reserved.