| Literature DB >> 21845579 |
Dilek Berker1, Serhat Isik, Yusuf Aydin, Yasemin Tutuncu, Gokhan Akdemir, Hatice Nursun Ozcan, Serdar Guler.
Abstract
Thyroid stimulating hormone (TSH) secreting pituitary adenomas are rare tumors manifested as hyperthyroidism with goiter in the presence of elevated TSH. We present a case with pituitary adenoma secreting both TSH and growth hormone (GH) with the prominent clinical findings of hyperthyroidism but without clinical findings of acromegaly. Pituitary magnetic resonance imaging revealed a macroadenoma. Transsphenoidal surgery was performed twice. The immunohistochemical staining showed that tumor cells were strongly reactive to GH and relatively mildly reactive to TSH. Control pituitary imaging revealed a residual macroadenoma, and long acting octreotide treatment was administered. After two years of the treatment, tumor size remained the same while thyroid function tests and insulin-like growth factor 1 (IGF-I) values returned to normal ranges. In conclusion, we always recommend hormonal examinations for all patients who have pituitary adenoma without signs and symptoms of acromegaly.Entities:
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Year: 2011 PMID: 21845579 DOI: 10.5137/1019-5149.JTN.2642-09.2
Source DB: PubMed Journal: Turk Neurosurg ISSN: 1019-5149 Impact factor: 1.003