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双侧先天性真皮样错构瘤覆盖角膜葡萄肿。

Bilateral, congenital, dermis-like choristomas overlying corneal staphylomas.

作者信息

Bernuy A, Contreras F, Maumenee A E, O'Donnell F E

出版信息

Arch Ophthalmol. 1981 Nov;99(11):1995-7. doi: 10.1001/archopht.1981.03930020871011.

Abstract

Two unrelated patients with diffuse, bilateral, congenital tumefactions overlying the corneas were seen. The tumors were protuberant, fleshy masses that partially concealed underlying corneal staphylomas. Spontaneous rupture was suspected in one eye. Histopathologic study of three specimens disclosed dermis-like tumors. In one specimen, an apocrine gland was identified, thus supporting the diagnosis of choristoma. An evisceration specimen from a ruptured globe confirmed that the ectatic cornea was an anterior staphyloma. The posterior pole seemed grossly normal. This disorder may have a genetic basis or it may result from a developmental or inflammatory insult in utero. Preoperative diagnosis is important because the associated anterior staphylomas complicate management.

摘要

我们遇到了两名不相关的患者,他们双眼角膜上方均有弥漫性、双侧先天性肿物。肿物为突出的肉质肿块,部分遮盖了下方的角膜葡萄肿。一只眼睛疑似发生了自发性破裂。对三个标本进行的组织病理学研究显示为类似真皮的肿瘤。在一个标本中发现了顶泌汗腺,从而支持了迷离瘤的诊断。一个眼球破裂后的眼球摘除标本证实扩张的角膜为前部葡萄肿。后极看起来大体正常。这种疾病可能有遗传基础,也可能是由子宫内的发育或炎症损伤所致。术前诊断很重要,因为相关的前部葡萄肿会使治疗复杂化。

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