| Literature DB >> 22930065 |
E M Valesky1, M Wahle, S Vranes, M Wolter, R Kaufmann, M Meissner.
Abstract
A 71-year-old woman developed progressive spreading of bitemporal scalp necrosis within 4 weeks accompanied by headaches, myalgia of the shoulder girdle and muscle weakness that had started a few months previously. No additional diseases were reported. The suspected temporal giant cell arteritis could be confirmed by temporal artery biopsy. Therapy with glucocorticoids led to a rapid resolution of clinical symptoms and was tapered over 18 months. Recovery of the scalp necrosis emerged following second intention healing and split-skin transplantation of necrotic areas after successful wound conditioning. The case study demonstrates a rare and serious complication of temporal arteritis which is often accompanied by a poor prognosis.Entities:
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Year: 2012 PMID: 22930065 DOI: 10.1007/s00393-012-1009-5
Source DB: PubMed Journal: Z Rheumatol ISSN: 0340-1855 Impact factor: 1.372