D. Calista et G. Landi, DISSEMINATED GRANULOMA-ANNULARE IN ACQUIRED-IMMUNODEFICIENCY-SYNDROME- CASE-REPORT AND REVIEW OF THE LITERATURE, Cutis, 55(3), 1995, pp. 158-160
The authors report the case of a 27-year-old woman who presented with
disseminated granuloma annulare in association with acquired immunodef
iciency syndrome. The lesions were asymptomatic, tiny, erythematous or
flesh-colored umbilicated papules on the neck, trunk, and flexor surf
ace of the arms and knees that regressed without any treatment in two
months. The case reported is the nineteenth description of the associa
tion of granuloma annulare and acquired immunodeficiency syndrome but
the first in a female patient. The causes and pathogenesis of granulom
a annulare are unknown, but after reviewing the previous case reports
we hypothesize that circulating human immunodeficiency virus particles
may be a precipitating factor in granuloma annulare and that the CD4 and CD8+ cell dysfunction may be responsible for the atypically short
course of the disease.