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多发性内分泌腺瘤病(MEN IIB)伴库欣综合征,由产生促肾上腺皮质激素释放激素的甲状腺髓样癌所致。

Multiple endocrine neoplasia (MEN IIB) with Cushing's syndrome due to medullary thyroid carcinoma producing corticotropin-releasing hormone.

作者信息

Tagliabue M, Pagani A, Palestini N, Manieri C, Martina V

机构信息

Department of Clinical Pathophysiology, University of Turin, Italy.

出版信息

Panminerva Med. 1996 Mar;38(1):41-4.

PMID:8766879
Abstract

We describe a case of Cushing's syndrome caused by a medullary thyroid carcinoma (MCT) secreting corticotropin-releasing-hormone (CRH) in a young woman presenting mucosal neuromas located on the top of the tongue and eyelid areas. Laboratory studies showed, basally and after dexamethasone suppression test, serum cortisol and plasma pituitary corticotrophin (ACTH) levels agreed with an ectopic Cushing's syndrome. Immunohistochemical studies of the MCT tissue revealed a production of CRH and scattered cells containing vasopressin but not ACTH peptides. This is the first demonstrated case of a CRH-secreting tumor in multiple endocrine neoplasia (MEN IIB) syndrome.

摘要

我们描述了一例年轻女性因分泌促肾上腺皮质激素释放激素(CRH)的甲状腺髓样癌(MCT)导致库欣综合征的病例,该女性在舌顶部和眼睑区域出现黏膜神经瘤。实验室研究表明,基础状态下以及地塞米松抑制试验后,血清皮质醇和血浆垂体促肾上腺皮质激素(ACTH)水平符合异位库欣综合征。对MCT组织进行免疫组化研究发现有CRH产生,且散在细胞含有血管加压素,但不含ACTH肽。这是多内分泌腺瘤病(MEN IIB)综合征中首例有证据证明的分泌CRH肿瘤病例。

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