Ormerod A D, Smart L, Reid T M, Milford-Ward A
Department of Dermatology, University of Aberdeen, United Kingdom.
Arch Dermatol. 1993 Mar;129(3):343-6. doi: 10.1001/archderm.129.3.343.
Familial cold urticaria is a rare cutaneous and systemic reaction to cold with autosomal dominant inheritance, distinctive clinical features, and unknown pathogenesis. Release of a chymotrypsinlike substance has been postulated. To date, no effective treatment has been reported.
Eight cases from a large family pedigree are described. Three members showed a very favorable response in their cold urticaria, when treated with stanozolol; the response was reproducible. Histologic examination of an early lesion in one case revealed evidence of mast cell degranulation.
The biochemical observations are probably secondary epiphenomena. Correction of a deficiency of an inhibitory protein is a possible mechanism of action of stanozolol as in hereditary angioedema.
家族性冷性荨麻疹是一种罕见的对寒冷的皮肤和全身反应,具有常染色体显性遗传、独特的临床特征且发病机制不明。有人推测会释放一种类胰凝乳蛋白酶物质。迄今为止,尚无有效治疗方法的报道。
描述了来自一个大家系的8个病例。3名成员在使用司坦唑醇治疗时,其冷性荨麻疹有非常良好的反应;该反应可重现。对1例早期皮损进行组织学检查发现肥大细胞脱颗粒的证据。
生化观察结果可能是继发性的附带现象。正如在遗传性血管性水肿中一样,纠正抑制蛋白缺乏可能是司坦唑醇的作用机制。