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Cushing's syndrome associated with corticogenic hypothyroidism: a case study.

作者信息

Inada M, Kurata S, Nishikawa M, Oishi M, Mashio Y, Tanaka K, Ishii H, Naito K, Imura H

出版信息

Endocrinol Jpn. 1981 Apr;28(2):225-30. doi: 10.1507/endocrj1954.28.225.

DOI:10.1507/endocrj1954.28.225
PMID:7308157
Abstract

Described here is a 27-year-old female, who had centripetal obesity, broad reddish-purple striae on the lower abdomen and hypertension. Serum cortisol levels, the results of a dexamethasone suppression test and an adrenal scintigram with 131I-19-iodocholesterol were all compatible with Cushing's syndrome due to an adrenal adenoma that secretes cortisol autonomously. This was confirmed by gross and microscopic examination of the removed adrenal tumor. In addition, the patient had markedly diminished T4 and T3 concentrations in serum. Basal TSH levels were not elevated and did not rise significantly after TRH injection. Serum T4 and T3 concentrations were elevated to the normal range when the hyperadrenocorticism was corrected. The results indicate that the patient had "'corticogenic hypothyroidism."

摘要

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引用本文的文献

1
Hypothalamic hypothyroidism due to isolated thyrotropin-releasing hormone (TRH) deficiency.由于孤立性促甲状腺激素释放激素(TRH)缺乏导致的下丘脑性甲状腺功能减退症。
J Endocrinol Invest. 1984 Jun;7(3):231-3. doi: 10.1007/BF03348429.