Literature DB >> 7096671

Giant cell arteritis: a systemic disease with rare cutaneous manifestations.

E W Baum, W M Sams, R R Payne.   

Abstract

Giant cell arteritis is a systemic disease usually occurring in patients in the fifth decade or older, more often in women. Dermatologic manifestations are rare but, when found, are usually expressed as scalp ulcerations or blanching associated with gangrene of the tongue. The dermatologist should be familiar with the entity because it is often more severe when associated with scalp necrosis, and prompt intervention with corticosteroids can prevent catastrophic sequelae.

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Year:  1982        PMID: 7096671     DOI: 10.1016/s0190-9622(82)70094-5

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  4 in total

1.  Giant cell arteritis of the skin simulating erythema nodosum.

Authors:  J W Goldberg; M L Lee; S M Sajjad
Journal:  Ann Rheum Dis       Date:  1987-09       Impact factor: 19.103

2.  Scalp necrosis and giant cell arteritis: case report and issues in wound management.

Authors:  Stefan J Landis; Susan Selinger; Norman Flett
Journal:  Int Wound J       Date:  2005-12       Impact factor: 3.315

Review 3.  Infiltrated papules on the trunk and headaches: A case of actinic granuloma and a review of the literature.

Authors:  Sonal A Parikh; Syril Keena T Que; William D Holmes; Katalin Ferenczi; Jane M Grant-Kels; Marti Jill Rothe
Journal:  Int J Womens Dermatol       Date:  2015-09-09

Review 4.  A Review of the Dermatological Complications of Giant Cell Arteritis.

Authors:  Diana Prieto-Peña; Santos Castañeda; Belén Atienza-Mateo; Ricardo Blanco; Miguel Ángel González-Gay
Journal:  Clin Cosmet Investig Dermatol       Date:  2021-03-25
  4 in total

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