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Pituitary Gangliocytoma Producing TSH and TRH: A Review of “Gangliocytomas of the Sellar Region”
Author(s) -
Kiyohiko Sakata,
Kana Fujimori,
Satoru Komaki,
Takuya Furuta,
Yasuo Sugita,
Kenji Ashida,
Masatoshi Nomura,
Motohiro Morioka
Publication year - 2020
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/clinem/dgaa474
Subject(s) - pituitary tumors , acromegaly , pituitary adenoma , medicine , chromophobe cell , pathology , endocrinology , pituitary gland , pituitary neoplasm , prolactinoma , thyrotropin releasing hormone , galactorrhea , adenoma , hormone , immunohistochemistry , prolactin , clear cell , growth hormone
Pituitary gangliocytomas (GCs) are rare neuronal tumors that present with endocrinological disorders, such as acromegaly, amenorrhea-galactorrhea syndrome, and Cushing's disease. Most pituitary GCs coexist with pituitary adenomas pathologically and are diagnosed as mixed gangliocytoma-adenomas. Herein, we report a case of 45-year-old man who presented with the syndrome of inappropriate secretion of thyroid-stimulating hormone (SITSH) and discuss the pathogenesis of pituitary GCs.

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