The Annals Holiday Offer - Save 50%
home help contact us subscription past issues search current issue
 QUICK SEARCH:   [advanced]


     



Published Online, 15 July 2008, www.theannals.com, DOI 10.1345/aph.1L215.
The Annals of Pharmacotherapy: Vol. 42, No. 9, pp. 1323-1326. DOI 10.1345/aph.1L215
© 2008 Harvey Whitney Books Company.
This Article
Right arrow Résumé Freely available
Right arrow Extracto Freely available
Right arrow Full Text
Right arrow PDF
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Articles Ahead of Print
Right arrow [Order Reprint]
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Te, C. C
Right arrow Articles by Allee, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Te, C. C
Right arrow Articles by Allee, M.

Famciclovir-Induced Leukocytoclastic Vasculitis

Charles C Te, MD

Resident, Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK

Vu Le, MD

Resident, Department of Medicine, University of Oklahoma Health Sciences Center

Mark Allee, MD

Assistant Professor, Department of Medicine, University of Oklahoma Health Sciences Center

Reprints: Dr. Te, Department of Internal Medicine, University of Oklahoma Health Sciences Center, PO Box 26901, WP 1140, Oklahoma City, Oklahoma 73190, fax 405/271-7186, charles-te{at}ouhsc.edu

OBJECTIVE: To report a case of famciclovir-induced leukocytoclastic vasculitis (LCV).

CASE SUMMARY: A 67-year-old white female presented to the hospital for evaluation of large, bilateral palpable purpura; coalescing ulcers with central eschars; and small, red violaceous papules on her legs and groin. Approximately 2 months prior to this hospitalization, the woman was diagnosed with shingles of her left T1–T2 nerve distribution and was treated with famciclovir 500 mg 3 times daily, which was her first exposure to this medication. Her shingles resolved; however, on day 4 of treatment, she began to notice red spots on both of her legs that began to progressively blister and increase in size. She discontinued famciclovir at that time. The rash persisted and spread to her abdomen, groin, legs, feet, and toes. She underwent punch biopsy that revealed LCV. Workup was negative for antinuclear antibody, rheumatoid factor, hepatitis B and C virus, perinuclear-staining antineutrophil cytoplasmic antibodies, cytoplasmic-staining antineutrophil cytoplasmic antibodies, antibodies to extractable nuclear antigens, proteinase 3, and myeloperoxidase. The patient improved with daily oral steroids and local wound care.

DISCUSSION: LCV has been reported only once before in the English literature as of January 2008. The most common cause of LCV is medication use, but it is a diagnosis of exclusion. It is hypothesized that drugs act as haptens, which cause an immune response. An objective causality assessment using the Naranjo probability scale suggested that famciclovir was the probable cause of LCV in this patient.

CONCLUSIONS: Healthcare professionals should be aware of the possible development of famciclovir-induced LCV.

Key Words: famciclovir, leukocytoclastic vasculitis

Published Online, July 15, 2008. www.theannals.com, DOI 10.1345/aph.1L215





homecopy help contact us subscription past issues search current issue
Copyright © 2008 by Harvey Whitney Books Company.