A case of coexistence of TSH/GH-secreting pituitary tumor and papillary thyroid carcinoma: Challenges in pathogenesis and management

Highlights • TSHoma commonly presents as a macroadenoma with the symptoms of hyperthyroidism. • TSHoma with concomitant hypersecretion of other pituitary hormones has been reported. • TSHoma and Acromegaly may increase the risk of thyroid carcinoma.

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Bibliographic Details
Published in:Journal of clinical neuroscience 2017-07, Vol.41, p.78-80
Main Authors: Kiatpanabhikul, Phatharaporn, Shuangshoti, Shanop, Chantra, Kraisri, Navicharern, Patpong, Kingpetch, Kanaungnit, Houngngam, Natnicha, Snabboon, Thiti
Format: Article
Language:English
Subjects:
Acromegaly
Carcinoma, Papillary - complications
Carcinoma, Papillary - diagnosis
Carcinoma, Papillary - etiology
Female
Growth Hormone-Secreting Pituitary Adenoma - complications
Growth Hormone-Secreting Pituitary Adenoma - diagnosis
Growth Hormone-Secreting Pituitary Adenoma - etiology
Humans
Hyperthyroidism - complications
Hyperthyroidism - diagnosis
Hyperthyroidism - etiology
Inappropriate TSH secretion
Middle Aged
Neurology
Pituitary Neoplasms - complications
Pituitary Neoplasms - diagnosis
Pituitary Neoplasms - etiology
Pituitary tumor
Thyroid Cancer, Papillary
Thyroid carcinoma
Thyroid Neoplasms - complications
Thyroid Neoplasms - diagnosis
Thyroid Neoplasms - etiology
Thyrotropin - blood
TSHoma
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Description
Summary:Highlights • TSHoma commonly presents as a macroadenoma with the symptoms of hyperthyroidism. • TSHoma with concomitant hypersecretion of other pituitary hormones has been reported. • TSHoma and Acromegaly may increase the risk of thyroid carcinoma.
ISSN:0967-5868
1532-2653
DOI:10.1016/j.jocn.2017.02.050