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毛囊角化性棘皮瘤性秃发(西门子综合征)伴其他异常

[Keratosis follicularis spinulosa decalvans (Siemens' syndrome) associated with other abnormalities].

作者信息

Domenech P, Ferrando J, Corretger M, Torras H, Valls X, González A

出版信息

Med Cutan Ibero Lat Am. 1985;13(2):175-81.

PMID:3900603
Abstract

Keratosis follicularis spinulosa decalvans (ichthyosis follicularis or Siemens's syndrome) is considered a general form of keratosis pilaris decalvans. Localized types are keratosis pilaris atrophicans and atrophoderma vermicularis. A case of this unusual process is presented. Clinical, histological and scanning electron microscopic studies of the hair were performed. Clinically, a generalized hypotrichosis with hyperkeratotic follicular plugs is observed; especially in the scalp and the eyebrows. Other interesting clinical findings were cutis hyperelastica, gingival hypertrophy, mongoloid palpebral fissures, big pinnae and clinodactyly of the 5th finger. From the histological point of view we observed follicular plugging, dystrophic pilosebaceous follicles, absence of sebaceous glands, perifollicular fibrosis and minimal lymphomonocytic infiltrate. Scanning electronmicroscopy shows a brittle hair with cuticular abnormalities. Siemens's syndrome can be considered a specific pilosebaceous dysplasia because the absence or hypoplasia of sebaceous glands; which produces follicular hyperkeratosis and pilar atrophy with perifollicular fibrosis and alopecia.

摘要

萎缩性毛囊角化病(毛囊性鱼鳞病或西门子综合征)被认为是萎缩性毛发角化病的一种常见形式。局限性类型为萎缩性毛发角化病和蠕虫状皮肤萎缩。本文报道了一例这种罕见病症。对毛发进行了临床、组织学和扫描电子显微镜研究。临床上,观察到全身毛发稀少伴有角化过度的毛囊性丘疹;尤其在头皮和眉毛部位。其他有趣的临床发现包括皮肤弹性过度、牙龈增生、蒙古样睑裂、大耳廓和第5指弯曲。从组织学角度观察到毛囊堵塞、营养不良性毛囊皮脂腺、皮脂腺缺失、毛囊周围纤维化和少量淋巴细胞浸润。扫描电子显微镜显示毛发脆弱且有角质层异常。西门子综合征可被视为一种特殊的毛囊皮脂腺发育异常,因为皮脂腺缺失或发育不全,从而导致毛囊角化过度和毛发萎缩,并伴有毛囊周围纤维化和脱发。

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