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[获得性副肿瘤性胎毛增多症伴硬皮病]

[Acquired paraneoplastic hypertrichosis lanuginosa associated with scleroderma].

作者信息

Valda Rodriguez L, Torrico Velasco J, Zeballos Vasconcellos R

机构信息

Service de dermatologie, Hospital de Clinicas, Universitario, La Paz, Bolivia.

出版信息

Ann Dermatol Venereol. 1990;117(9):605-10.

PMID:2260800
Abstract

Acquired hypertrichosis lanuginosa is universally recognized as an individual disease and seldom reported as a genuine paraneoplastic manifestation. We report the case of a 30-year old woman with acquired hypertrichosis lanuginosa. Due to the finding of a cervical lymph node metastasis, she was investigated for an internal neoplasm, but the original tumour could not be found by the usual methods. A bronchogenic carcinoma was discovered at autopsy. Beside hypertrichosis, this patient had other disorders not described in the literature as associated with that disease, viz.: progressive systemic scleroderma, fissured and hyperpigmented tongue, thrombocytopenia, galactorrhoea, axillary and pubic alopecia and overcurvature of toe nails. A review of similar cases in the literature provided clinical arguments in favour of the hormonal origin of this paraneoplastic hypertrichosis.

摘要

获得性毳毛增多症被公认为一种独立疾病,很少作为真正的副肿瘤表现被报道。我们报告一例30岁获得性毳毛增多症女性病例。因发现颈部淋巴结转移,对其进行了内部肿瘤的检查,但通过常规方法未发现原发肿瘤。尸检时发现为支气管源性癌。除毳毛增多外,该患者还有一些文献中未描述与该病相关的其他病症,即:进行性系统性硬化症、舌裂和色素沉着、血小板减少、溢乳、腋窝和耻骨部脱发以及脚趾甲过度弯曲。对文献中类似病例的回顾提供了支持这种副肿瘤性毳毛增多症激素起源的临床依据。

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