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一名70多岁的男性,患有鞍区肿物。

A man in his mid-70s with a sellar mass.

作者信息

Jung Shih-Ming, Hsu Yuan-Yu, Chuang Chi-Cheng, Chang Chen-Nen, Hsueh Chuen, Kuo Tseng-tong

出版信息

Brain Pathol. 2007 Jan;17(1):115-6, 121. doi: 10.1111/j.1750-3639.2007.00044_1.x.

Abstract

Metastatic melanoma to a pituitary oncocytoma is a very rare condition. A 76-year-old man was presented with progressive visual disturbance and falling down with initial loss of consciousness 2 days before admission. He had a subungual acral lentiginous melanoma (T3N1M0) with gangrenous change of left big toe, treated by amputation 15 months ago. Computed tomography and MR imaging demonstrated masses involving inguina, mediastinum and left renal hilum and dumb-bell shaped hyperdense mass, approximately 6.2 x 3.7 mm, that involved pituitary fossa and suprasellar region with adjacent bony destruction. He underwent surgical resection of the tumor. Microscopically, the tumor revealed an admixture of pituitary adenoma and invasive metastatic melanoma with fragments containing both populations in juxtaposition. The adenoma was negative for melanoma markers and pituitary hormone markers. The melanoma was positive for S-100 protein and BMB-45. Ultrastructure of the adenoma revealed abundant mitochondria and sparse secretory granules. The diagnosis was metastatic melanoma to a pituitary oncocytoma. The current literature on metastatic tumors to pituitary adenoma is reviewed.

摘要

黑色素瘤转移至垂体嗜酸性细胞瘤是一种非常罕见的情况。一名76岁男性在入院前2天出现进行性视力障碍,并伴有最初的意识丧失和跌倒。他15个月前因左大脚趾坏疽性改变接受了截肢手术,患有甲下肢端雀斑样黑色素瘤(T3N1M0)。计算机断层扫描和磁共振成像显示肿块累及腹股沟、纵隔和左肾门,以及哑铃状高密度肿块,大小约6.2×3.7毫米,累及垂体窝和鞍上区域并伴有相邻骨质破坏。他接受了肿瘤的手术切除。显微镜下,肿瘤显示为垂体腺瘤和浸润性转移性黑色素瘤的混合,碎片中两种成分并列存在。腺瘤对黑色素瘤标志物和垂体激素标志物均为阴性。黑色素瘤对S-100蛋白和BMB-45呈阳性。腺瘤的超微结构显示线粒体丰富,分泌颗粒稀少。诊断为黑色素瘤转移至垂体嗜酸性细胞瘤。本文对目前关于垂体腺瘤转移性肿瘤的文献进行了综述。

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