[Bitemporal scalp necrosis : a very rare manifestation of giant cell arteritis]

Z Rheumatol. 2012 Nov;71(9):806-9. doi: 10.1007/s00393-012-1009-5.
[Article in German]

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.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Diagnosis, Differential
  • Female
  • Giant Cell Arteritis / complications*
  • Giant Cell Arteritis / diagnosis
  • Giant Cell Arteritis / drug therapy*
  • Glucocorticoids / therapeutic use*
  • Humans
  • Middle Aged
  • Necrosis
  • Scalp / drug effects*
  • Scalp / pathology*
  • Scalp Dermatoses / drug therapy*
  • Scalp Dermatoses / etiology
  • Scalp Dermatoses / pathology*
  • Treatment Outcome

Substances

  • Glucocorticoids