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[嗜铬细胞瘤与自身免疫性甲状腺功能减退症]

[Pheochromocytoma and autoimmune hypothyroidism].

作者信息

Bartolomei C, Gianchecchi D, Chiavistelli P, Lenzi R

机构信息

Divisione di Medicina Interna, Ospedale Civile di Rosignano Solvay, Livorno.

出版信息

Minerva Med. 1992 Jul-Aug;83(7-8):485-6.

PMID:1522975
Abstract

The association of multiple endocrine diseases is frequent and the coincidental involvement of the thyroid and adrenal glands is well recognized. On the contrary, two cases of hypo or hyperthyroidism have only been reported in literature: one concerning adrenal pheochromocytoma with simultaneous autoimmune hypothyroidism and another of a diffuse toxic goiter associated with pheochromocytoma. The purpose of the present report is to point out a new case of a pheochromocytoma associated with an autoimmune hypothyroidism in which the latter is florid and not biochemical.

摘要

多种内分泌疾病并存的情况很常见,甲状腺和肾上腺同时受累已得到充分认识。相反,文献中仅报道过两例甲状腺功能减退或亢进的病例:一例是肾上腺嗜铬细胞瘤合并自身免疫性甲状腺功能减退,另一例是弥漫性毒性甲状腺肿合并嗜铬细胞瘤。本报告的目的是指出一例与自身免疫性甲状腺功能减退相关的嗜铬细胞瘤新病例,其中自身免疫性甲状腺功能减退表现明显而非仅为生化指标异常。

相似文献

1
[Pheochromocytoma and autoimmune hypothyroidism].[嗜铬细胞瘤与自身免疫性甲状腺功能减退症]
Minerva Med. 1992 Jul-Aug;83(7-8):485-6.
2
[Pheochromocytoma and multinodular toxic goiter: an infrequent association].
Med Clin (Barc). 1990 Oct 27;95(14):559.
3
[Bilateral adrenal pheochromocytoma. A clinical case and review of the literature].
Minerva Chir. 1997 May;52(5):667-72.
4
[Report of a case of malignant vesical pheochromocytoma. Diagnosis and therapy].[一例恶性膀胱嗜铬细胞瘤的病例报告。诊断与治疗]
Ann Urol (Paris). 1990;24(5):396-9.
5
[New issues in surgery of adrenal pheochromocytoma].[肾上腺嗜铬细胞瘤手术的新问题]
G Chir. 1999 Jan-Feb;20(1-2):57-62.
6
Coexistence of MEN 2A and papillary thyroid carcinoma and a recurrent pheochromocytoma 23 years after surgery: report of a case and a review of the Japanese literature.MEN 2A与甲状腺乳头状癌并存及术后23年复发性嗜铬细胞瘤:1例报告并文献复习
Jpn J Clin Oncol. 1995 Aug;25(4):153-8.
7
Pheochromocytoma in pregnancy--a case report and review of the literature.妊娠期嗜铬细胞瘤——一例病例报告及文献综述
Acta Obstet Gynecol Scand. 2000 Aug;79(8):709-11.
8
[A case of Sipple syndrome whose bilateral pheochromocytomas were resected separately after a 3-year interval].1例双侧嗜铬细胞瘤间隔3年先后切除的西普尔综合征病例
Hinyokika Kiyo. 2000 Apr;46(4):251-3.
9
[The characteristics of the course and diagnostic difficulties in pheochromocytoma in young people].
Ter Arkh. 1996;68(4):80-2.
10
[Extra-adrenal pheochromocytoma. (apropos of a case surgically treated and cured)].
Dakar Med. 1979;24(2):212-9.

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Clin Case Rep. 2019 Mar 2;7(4):726-730. doi: 10.1002/ccr3.2065. eCollection 2019 Apr.
2
Bilateral pheochromocytoma: Two tumors may not be same!双侧嗜铬细胞瘤:两个肿瘤可能不一样!
Anesth Essays Res. 2015 Sep-Dec;9(3):451-2. doi: 10.4103/0259-1162.159772.
3
Pheochromocytoma presenting as recurrent urinary tract infections : a case report.表现为复发性尿路感染的嗜铬细胞瘤:一例报告
J Med Case Rep. 2011 Jan 12;5:6. doi: 10.1186/1752-1947-5-6.