A 90-year-old woman presented to the emergency department complaining of a 3-month history of headache and recent blindness of her right eye. She also reported weakness and weight loss (5 kg during the last 3 months before her presentation) but no fever. She had been treated symptomatically with nonsteroidal antiinflammatory drugs without noting any significant relief. There was no history of trauma or burn. Her past medical history included diabetes mellitus type II and arterial hypertension. The physical examination on presentation was unremarkable except for a large area of scalp necrosis in the temporoparietal region bilaterally (Fig. 1).
Routine laboratory testing on admission showed anemia (hematocrit=31,1%) and elevated erythrocyte sedimentation rate (ESR=120 mm/first hour). Serological tests for Varicella–Zoster virus (VZV) and herpes simplex virus 1 and 2 (HSV1 and HSV2) were negative. A computed tomography scan of the head was unremarkable. The patient underwent biopsy of the right temporal artery, which showed typical changes of temporal arteritis. She was given treatment with oral steroids (48 mg/day). After 2 months, the crusting area of the scalp diminished and the ESR normalized (ESR=20 mm/h). Scalp necrosis is a rare but severe complication of temporal arteritis. It is associated with a bad prognosis because it is usually a manifestation of severe, occlusive vasculitis or a result of delayed recognition of temporal arteritis [1]. Adequate corticosteroid therapy is mandatory [2].
References
Vamma R, Patel A (2005) Scalp lesions in a 78-year-old woman. CMAJ 173:33
Currey J (1997) Scalp necrosis in giant cell arteritis and review of the literature. Br J Rheumatol 36:814–816
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Manetas, S., Moutzouris, D.A. & Falagas, M.E. Scalp necrosis: a rare complication of temporal arteritis. Clin Rheumatol 26, 1169 (2007). https://doi.org/10.1007/s10067-006-0294-2
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DOI: https://doi.org/10.1007/s10067-006-0294-2