Skip to main content
Deutsches Ärzteblatt International logoLink to Deutsches Ärzteblatt International
letter
. 2021 Sep 24;118(38):644. doi: 10.3238/arztebl.m2021.0081

Scalp Necrosis in the Context of Giant Cell Arteritis

Phuong Nguyen *, Matthias Pierer *, Christoph Baerwald *
PMCID: PMC8715313  PMID: 34857073

An 85-year-old male patient presented with progressive bitemporal necrosis of the scalp. Six months previously, he had been diagnosed with giant cell arteritis based on ultrasound evidence of vasculitis of both temporal arteries. The patient initially presented with typical symptoms including headache, jaw claudication and transient visual impairment. These symptoms dissolved after the initiation of treatment with predisolone 500 mg and did not occur again under steroid tapering. A few weeks ago, he first noticed black lesions on his scalp. The lesions became inflamed, grew in size and became encrusted over time. The diagnosis of scalp necrosis as a rare manifestation of giant cell arteritis was made. Only about 100 cases have been reported in the literature to date, none of which is known to show an onset of necrosis under ongoing corticosteroid therapy. Our patient received 20 mg prednisolone over three weeks, followed by cautious dose reduction. The cutaneous finding was first stable under this therapy, then showed slow signs of healing. To speed up the healing process, necrotic areas were surgically removed by a dermatologist.

Translated from the original German by Christine Rye.

Figure.

Figure

Footnotes

Conflict of interest statement: The authors declare that no conflict of interest exists.


Articles from Deutsches Ärzteblatt International are provided here courtesy of Deutscher Arzte-Verlag GmbH

RESOURCES