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垂体嫌色细胞瘤伴库欣综合征及皮肤色素沉着

Chromophobe adenoma of the pituitary with Cushing's syndrome and skin pigmentation.

作者信息

Sterling N, Hall M R

出版信息

Postgrad Med J. 1979 Sep;55(646):564-6. doi: 10.1136/pgmj.55.646.564.

Abstract

A 76-year-old man with pigmentation and Cushing's disease is described, who was found to have a large chromophobe adenoma of the pituitary. Despite normal skull X-rays the presence of bitemporal hemianopia led to the diagnosis which was later confirmed at post-mortem. Adrenalectomy performed in the treatment of Cushing's disease may be followed by skin pigmentation and an enlarging pituitary tumour (Nelson's syndrome), changes which are commonly attributed to the removal of the negative feed-back mechanism. The spontaneous occurrence of these changes in this patient who did not undergo adrenalectomy supports the view that a pituitary tumour pre-exists in cases of Nelson's syndrome and emphasizes the importance of directing initial treatment to the pituitary.

摘要

本文描述了一名患有色素沉着和库欣病的76岁男性,其被发现患有垂体大嫌色细胞瘤。尽管颅骨X线检查正常,但双侧颞侧偏盲的存在导致了该诊断,后来在尸检时得到证实。为治疗库欣病而进行的肾上腺切除术可能会继发皮肤色素沉着和垂体肿瘤增大(尼尔森综合征),这些变化通常归因于负反馈机制的消除。该未接受肾上腺切除术的患者自发出现这些变化,支持了尼尔森综合征病例中垂体肿瘤预先存在的观点,并强调了针对垂体进行初始治疗的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b95c/2428093/d74d74383d2d/postmedj00248-0054-a.jpg

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本文引用的文献

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