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[颗粒状角化不全]

[Granular parakeratosis].

作者信息

González de Arriba M, Vallés-Blanco L, Polo-Rodríguez I, Rosales-Trujillo B, Ortiz de Frutos F J, Rodríguez-Peralto J L, Vanaclocha-Sebastián F

机构信息

Servicio de Dermatología, Hospital Universitario 12 de Octubre, Madrid.

出版信息

Actas Dermosifiliogr. 2007 Jun;98(5):355-7. doi: 10.1016/s0001-7310(07)70081-9.

Abstract

Granular parakeratosis is a rare entity that results from an acquired disorder of keratinization. Clinically presents as dark erythematous plaques, occasionally pruritic, that usually involve the axilla and other intertriginous areas. The pathology is characteristic and consists of thickening of the stratum corneum with compact parakeratosis and retention of keratohyaline granules, whereas the stratum granulosum is preserved. The etiology is unknown although some factors such as irritating physical or chemical agents have been implicated. Treatment response is variable. We report a new case in a 50-year-old woman with brownish and hyperkeratotic plaques on both axillae, of two years duration, with a compatible pathology that showed a favorable response to tacalcitol.

摘要

颗粒状角化不全是一种由后天性角化异常引起的罕见病症。临床上表现为暗红色斑片,偶有瘙痒,通常累及腋窝及其他皮肤褶皱部位。其病理特征为角质层增厚伴致密角化不全及透明角质颗粒留存,而颗粒层保留。病因不明,尽管一些因素如刺激性物理或化学制剂被认为与之有关。治疗反应不一。我们报告一例50岁女性的新病例,其双侧腋窝有持续两年的褐色及角化过度斑片,病理结果与之相符,对他卡西醇治疗反应良好。

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