Barr C C, Green W R, Payne J W, Knox D L, Jensen A D, Thompson R L
Surv Ophthalmol. 1975 Jan-Feb;19(4):224-39.
Four patients with primary intraocular reticulum-cell sarcoma were presented. All of the patients were followed at the Wilmer Institute for periods of up to ten years. All had decreased visual acuity and a uveitis that was refractory to standard forms of therapy. In one case, the correct diagnosis was made clinically. At autopsy, two of the patients had systemic reticulum-cell sarcoma, a third had intracranial reticulum-cell sarcoma, and in a fourth case the disease process was confined to the eye. The literature is reviewed and the clinico-pathologic features of the total of 14 cases are analyzed. It is emphasized that a recalcitrant uveitis was present in almost all of the cases reported. Differential diagnosis and methods of diagnosis are discussed.
本文报告了4例原发性眼内网状细胞肉瘤患者。所有患者均在威尔默眼科研究所接受了长达10年的随访。所有患者均有视力下降和对标准治疗形式难治的葡萄膜炎。其中1例在临床上做出了正确诊断。尸检时，2例患者有全身性网状细胞肉瘤，第3例有颅内网状细胞肉瘤，第4例疾病过程局限于眼部。本文回顾了文献并分析了总共14例病例的临床病理特征。强调几乎所有报告的病例中都存在顽固性葡萄膜炎。讨论了鉴别诊断和诊断方法。
