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A clone of elusive parents: Gonadotroph adenomafemale type

机译:难以捉摸的父母的克隆:性腺营养腺腺瘤女性型

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摘要

A 69-year-old woman presented with visual disturbance. Perimetry testing revealed a bitemporal hemianopia. Brain MRI demonstrated a 2.2-cm gadolinium-enhancing pituitary mass. Previously she had been treated for hypothyroidism, hypertension, and dyslipidemia. She had hyperprolactinemia. Endoscopic transsphenoidal debulking improved her visual field defects. Histology showed a chromophobic adenoma. Electron microscopy showed elongated, polar cells with long, slender processes. The small uniform secretory granules were peripherally disposed, collecting heavily within cell processes. Based on electron microscopical characteristics the tumor is consistent with an ACTH-negative female gonadotroph adenoma. The parent cell of this rare variant of a pituitary adenoma is yet unknown.
机译:一名69岁的女性出现视力障碍。视野测定法显示存在双颞偏盲。脑部MRI显示2.2厘米的g垂体肿块。以前,她曾接受甲状腺功能减退,高血压和血脂异常的治疗。她患有高泌乳素血症。内镜下经蝶窦下体改善了她的视野缺损。组织学显示发色性腺瘤。电子显微镜显示细长的极性细胞具有长而细长的过程。小而均匀的分泌颗粒被外围放置,在细胞过程中大量聚集。基于电子显微镜特征,该肿瘤与ACTH阴性雌性性腺营养腺瘤一致。这种罕见的垂体腺瘤变体的亲本细胞尚不清楚。

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