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结膜孤立性角化棘皮瘤:1例报告

Solitary keratoacanthoma of the conjunctiva: report of a case.

作者信息

Tulvatana W, Pisarnkorskul P, Wannakrairot P

机构信息

Department of Ophthalmology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

J Med Assoc Thai. 2001 Jul;84(7):1059-64.

Abstract

Keratoacanthoma characteristically occurs on the skin and is rarely found in the conjunctiva. We, herein, report a case of a healthy 41-year-old Thai woman presenting with a rapidly growing conjunctival mass. The tumor was excised to exclude squamous cell carcinoma. Histopathology revealed a cup shaped well-circumscribed proliferation of squamous cells, with a central keratin crater, consistent with a keratoacanthoma. On the literature review, only 12 cases have previously been reported in the English language. The mean age of presentation was 40.75 years, with a male preponderance. Presentation of a mass was mostly within 4 weeks after onset. History of foreign material getting into the eye was positive in 5 cases. All cases were successfully treated by excision, except for one case in which malignancy transformation was found, and enucleation was required eventually. Conjunctival keratoacanthoma is a rare disease. However, this lesion should be well recognized and not misinterpreted as malignancy. As far as we are aware, this is the first report of conjunctival keratoacanthoma from this region.

摘要

角化棘皮瘤通常发生于皮肤,很少见于结膜。在此,我们报告一例41岁健康泰国女性,其结膜出现迅速生长的肿物。切除该肿瘤以排除鳞状细胞癌。组织病理学显示为杯状、边界清楚的鳞状细胞增生,中央有角质栓,符合角化棘皮瘤。经文献检索,此前仅有12例英文报道。发病的平均年龄为40.75岁,男性居多。肿物大多在发病后4周内出现。5例有异物入眼史。除1例发生恶变最终需要眼球摘除术外,所有病例均通过切除成功治愈。结膜角化棘皮瘤是一种罕见疾病。然而,这种病变应得到充分认识,不应误诊为恶性肿瘤。据我们所知,这是该地区关于结膜角化棘皮瘤的首例报告。

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