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[一个家族中同时出现肢端早老症和Gottron型肢端早老症]

[Simultaneous occurrence of metageria and Gottron's acrogeria in one family].

作者信息

Kaufmann I, Thiele B, Mahrle G

出版信息

Z Hautkr. 1985 Jun 15;60(12):975-84.

PMID:4024679
Abstract

We report on a 17-year-old patient suffering from generalized mottled hyperpigmentation and multiple telangiectatic lesions of the skin. The subcutaneous fatty tissue was lacking or deficient. The patient showed a bird-like face. The cutaneous changes had been present since birth. X-ray studies revealed acro-osteolysis of the hands and feet. The metabolic and endocrine data were within normal ranges except of latent hypothyroidism. The clinical picture presented all criteria of metageria. The patient's mother and sister showed similar cutaneous changes, however, restricted to the distal parts of the extremities. We diagnosed acrogeria Gottron. The incidence of both metageria and acrogeria in one family makes metageria as an independent entity doubtful.

摘要

我们报告了一名17岁的患者,患有全身性斑驳性色素沉着和多处皮肤毛细血管扩张性病变。皮下脂肪组织缺乏或不足。患者呈现出鸟样面容。皮肤变化自出生就存在。X线检查显示手足肢端骨质溶解。代谢和内分泌数据除潜在甲状腺功能减退外均在正常范围内。临床表现符合早老症的所有标准。患者的母亲和姐姐有类似的皮肤变化,但仅限于肢体远端。我们诊断为戈特龙肢端早老症。一个家族中同时出现早老症和肢端早老症的情况使得早老症作为一个独立实体存在疑问。

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引用本文的文献

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