Zahorcsek Z, Schneider I
Department of Dermatology, University Medical School of Pecs, Hungary.
Dermatology. 1994;189(3):286-8. doi: 10.1159/000246863.
Multiple familial cutaneous telangiectases occurring over 3 generations are reported. The morphology of the lesions, the absence of haemorrhagic episodes and the pattern of inheritance are consistent with the diagnosis of hereditary benign telangiectasia described by Ryan and Wells. The differential diagnosis and a possible association with other mesodermal anomalies are discussed.
据报道，三代人出现了多发性家族性皮肤毛细血管扩张症。病变的形态、无出血发作以及遗传模式与Ryan和Wells所描述的遗传性良性毛细血管扩张症的诊断相符。文中讨论了鉴别诊断以及与其他中胚层异常可能存在的关联。
