Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2014) 35 P279 | DOI: 10.1530/endoabs.35.P279

ECE2014 Poster Presentations Clinical case reports Thyroid/Others (72 abstracts)

Three endocrine neoplasms: an unusual combination of pituitary adenoma, papillary thyroid carcinoma, and follicular thyroid carcinoma

Mina Gulfem Kaya 1 , Fatma Dilek Dellal 1 , Cafer Kaya 1 , Canan Altunkaya 2 , Reyhan Ersoy 1, & Bekir Cakir 1,


1Department of Endocrinology and Metabolism, Ataturk Education and Research Hospital, Ankara, Turkey; 2Department of Pathology, Ataturk Education and Research Hospital, Ankara, Turkey; 3Department of Endocrinology and Metabolism, Faculty of Medicine, Yildirim Beyazit University, Ankara, Turkey.


Background: Differentiated thyroid cancer is the most frequent thyroid tumor. Combinations of follicular carcinoma and papillary carcinoma are seen. Functional pituitary adenoma coexisting with differentiated thyroid carcinoma was reported previously in literature. We report a 47-year-old women with three different synchronous endocrine tumors; papillary thyroid cancer, follicular thyroid cancer, and prolactinoma.

Case: A 47-years-old female patient was admitted to out-patient clinic with oligomenorrhea and galactorrhea. Except patient’s prolactin (PRL) raise, hormonal levels were in normal ranges (PRL: 186 ng/ml). Macroprolactin was negative. Pituitary MRI demonstrated a mass 9×11 mm. Cabergolin 0.5 mg/ twice a week was started. She was euthyroid and thyroid autoantibodies were in normal ranges. In thyroid US, 17×10 mm nodule in left lobule, 21×19 mm nodule in right lobule, and 8×7 mm nodule in isthmus were detected. Fine needle aspiration biopsy suggested suspicious for follicular neoplasm for nodule in right lobule, benign for left one. She underwent total thyroidectomy. The histopathological examination revealed presence of a follicular cancer within right lobule (2 cm) and multifocal papillary cancer (0.5, 0.8, and 1.2 cm) within left lobule. Radioactive iodine was given to patient after surgery.

Conclusion: Underlying pathological cause of most pituitary adenomas remains unclear despite the recent identification of a number of potential molecular genetic abnormalities. Pituitary tumor transforming gene (PTTG) initially isolated from pituitary tumor cells. PTTG protein is expressed at higher than normal levels in several tumors, including those of the pituitary, thyroid, colon, ovary, testis, breast, and hematopoietic neoplasms. Co-existence of three endocrine tumors in our case may be caused from different causes. It may be releated with the potential molecular genetic abnormalities like PTTG. Or, incidental occurrence of them may be a reason, because each tumor occurs with a high prevalence in population.

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