Nasally located ectopic ACTH-secreting pituitary adenoma (EAPA) causing Nelson’s syndrome: diagnostic challenges

被引：0

作者：

K. Gurazada

A. Ihuoma

M. Galloway

N. Dorward

T. Wilhelm

B. Khoo

P. M. G. Bouloux

机构：

[1] University College London,Centre for Neuroendocrinology

[2] Royal Free Hospital,Department of Cellular Pathology

[3] UCL Medical School,Department of Neurosurgery

[4] Royal Free Hospital,Department of Radiology

来源：

Pituitary | 2014年 / 17卷

关键词：

Ectopic ACTH adenoma; ACTH-secreting ectopic adenoma; Nasal ectopic pituitary adenoma; Nelson’s syndrome;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：423 / 429

页数：6

共 30 条

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[23] Preoperative management of patients with ectopic Cushing's syndrome caused by ACTH-secreting pheochromocytoma: a case series and review of the literature
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[24] Preoperative management of patients with ectopic Cushing’s syndrome caused by ACTH-secreting pheochromocytoma: a case series and review of the literature
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[25] Ectopic Cushing's Syndrome Due to a Bronchial ACTH-Secreting Carcinoid Successfully Treated with Radio Frequency Ablation (RFA)
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[26] Nail hyperpigmentation in ACTH-secreting pituitary adenoma (Cushing's disease) and its resolution after successful trans-sphenoidal excision
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[27] Ectopic Cushing's syndrome from an ACTH-producing pheochromocytoma with a non-functioning pituitary adenoma
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[28] Pitfalls in the Diagnosis of Cushing's syndrome - a rare Case of an ectopic ACTH-Producing Pituitary Adenoma in the Sphenoid Sinus
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[29] Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing's syndrome and unusual histologic features
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[30] Lack of Mutations in the Gene Coding for the Glucocorticoid Receptor (NR3C1) in a Pediatric Patient with an ACTH-Secreting Pituitary Adenoma, Absence of Stigmata of Cushing Syndrome, and Unusual Histologic Features.
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