Lahoud S, Brownstein S, Laflamme M Y
Department of Ophthalmology, McGill University, Royal Victoria Hospital, Montreal, Quebec, Canada.
Am J Ophthalmol. 1988 Nov 15;106(5):579-83. doi: 10.1016/0002-9394(88)90589-2.
An 11-year-old boy and a 28-year-old woman each had a painless, slowly enlarging, elevated, yellow lesion of the inferior corneoscleral limbus and adjacent cornea and conjunctiva of the left eye. Histopathologic examination of both lesions disclosed involvement of the conjunctival substantia propria and the adjacent limbal and peripheral corneal stroma by a nonencapsulated, dense infiltrate composed of elongated fibrocytic cells, plump histiocytic cells occasionally with a vacuolated cytoplasm, some multinucleated giant cells, and scattered lymphocytes. The diagnosis in each case was fibrous histiocytoma. Both patients were otherwise in good health with no dermatologic, systemic, or other ocular abnormalities.
一名11岁男孩和一名28岁女性左眼的角膜巩膜缘下部及相邻角膜和结膜均出现了无痛性、缓慢增大、隆起的黄色病变。对这两处病变进行组织病理学检查发现，结膜固有层以及相邻的角膜缘和周边角膜基质有非包膜性致密浸润，浸润由细长的纤维细胞、偶尔有含空泡细胞质的丰满组织细胞、一些多核巨细胞和散在淋巴细胞组成。每例诊断均为纤维组织细胞瘤。两名患者其他方面健康，无皮肤、全身或其他眼部异常。
