Bardenstein D S, Char D H, Jones C, Crawford J B, Miller T R, Riekhof F T
Department of Ophthalmology, University of California, San Francisco 94143.
Arch Ophthalmol. 1990 Nov;108(11):1590-4. doi: 10.1001/archopht.1990.01070130092038.
A 50-year-old man with a history of systemic carcinoid had decreased right eye vision and a darkly pigmented cilio-choroidal mass. Results of ultrasonographic and fluorescein angiographic examinations were consistent with a malignant melanoma. Fine-needle aspiration biopsy of the lesion identified it as a carcinoid metastasis. The patient refused both radiation and enucleation; complete excision with a cyclochoroidectomy was performed. Histopathologic examination showed a carcinoid neoplasm covered by marked hyperplasia of the retinal pigment epithelium that produced the pigmented appearance of the lesion.
一名有系统性类癌病史的50岁男性,右眼视力下降,睫状体脉络膜有色素沉着的肿物。超声检查和荧光素血管造影检查结果与恶性黑色素瘤相符。对该病变进行细针穿刺活检,确定为类癌转移。患者拒绝放疗和眼球摘除术;遂行睫状体脉络膜切除术完整切除病变。组织病理学检查显示,类癌肿瘤被视网膜色素上皮显著增生覆盖,这导致了病变的色素沉着外观。