Khiari S, Ben Becher S, Souissi K, Dey D, Boudhina T
Service de Pédiatrie, Hôpital d'Enfants, Tunis Jebbari.
Ann Pediatr (Paris). 1990 Oct;37(8):511-2.
The authors report the case of a thirteen-year-old girl who developed clinical manifestations suggestive of Schönlein-Henoch purpura and in whom biologic tests outruled this condition and led to the diagnosis of Waldenström hyperglobulinemic purpura. Investigations illustrated the immunologic nature of this disease, outruled an underlying disease and established the diagnosis of primary hyperglobulinemic purpura.
作者报告了一例13岁女孩的病例,该女孩出现了提示过敏性紫癜的临床表现,但生物学检查排除了这种情况,并最终诊断为华氏巨球蛋白血症性紫癜。检查揭示了该疾病的免疫性质,排除了潜在疾病,并确立了原发性巨球蛋白血症性紫癜的诊断。