Literature DB >> 31678922

Scalp ulceration: a rare manifestation of giant cell arteritis.

Louise McDonald1, Gavin Baker2, Olga Kerr3.   

Abstract

An 81-year-old woman presented with an enlarging, tender ulcer on her scalp over an 8-week period, attributing it to a prior graze with garden shears. C-reactive protein and erythrocyte sedimentation rate were elevated at 87.7 mg/L and 112 mm/hour, respectively. Incisional biopsies demonstrated ulceration and full thickness necrosis with no evidence of malignancy. Vasculitis was suggested as a likely cause of such extensive necrosis and subsequent temporal artery biopsy findings were consistent with giant cell arteritis. The patient was initially treated with high-dose oral prednisolone and achieved complete healing of the scalp necrosis within 12 months, with a gradual down-titration of steroid therapy thereafter. Scalp necrosis is a rare, potentially life-threatening complication of giant cell arteritis. This case highlights the importance of considering scalp necrosis as a manifestation of giant cell arteritis when assessing scalp ulceration. Prompt diagnosis and treatment can prevent significant morbidity and potential mortality. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

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Keywords:  dermatology; rheumatology; skin; vasculitis

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Year:  2019        PMID: 31678922      PMCID: PMC6827760          DOI: 10.1136/bcr-2019-230795

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  1 in total

1.  Localized livedo racemosa as an indicator for giant cell arteritis.

Authors:  Katharina Drerup; Marcus Both; Thomas Schwarz
Journal:  JAAD Case Rep       Date:  2022-04-26
  1 in total

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