Case Report
Copyright ©2014 Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. May 16, 2014; 2(5): 151-156
Published online May 16, 2014. doi: 10.12998/wjcc.v2.i5.151
Parathyroid carcinoma in pregnancy
Maja Baretić, Hrvojka Tomić Brzac, Margareta Dobrenić, Antonia Jakovčević
Maja Baretić, Division of Endocrinology, Department of Internal Medicine, University Hospital Centre Zagreb, 10000 Zagreb, Croatia
Hrvojka Tomić Brzac, Margareta Dobrenić, Clinical Department of Nuclear Medicine and Radiation Protection, University Hospital Centre Zagreb, 10000 Zagreb, Croatia
Antonia Jakovčević, Department of Pathology and Cytology, University Hospital Centre Zagreb, 10000 Zagreb, Croatia
Author contributions: Baretić M wrote and designed the report, was responsible for the patient treatment and follow up, analyzed the data and wrote the paper; Tomić Brzac H performed and commented on the ultrasound exam; Dobrenić M performed and commented on the nuclear medicine exam; and Jakovčević A performed the pathology report analysis and made comments.
Correspondence to: Maja Baretić, MD, PhD, Division of Endocrinology, Department of Internal Medicine, University Hospital Centre Zagreb, Zavod za endokrinologiju Kišpatićeva 12, 10000 Zagreb, Croatia. maja.simek@zg.t-com.hr
Telephone: +385-98-412284 Fax: +385-1-2376036
Received: December 24, 2013
Revised: March 20, 2014
Accepted: April 3, 2014
Published online: May 16, 2014
Abstract

A 24-year-old female patient with parathyroid carcinoma, the rarest endocrine malignancy, had two pregnancies. In the first pregnancy, she had severe nausea and fatigue. Hypercalcemia and hyperparathyroidism were diagnosed in the postpartum period. Hyperemesis gravidarum masked a diagnosis of hypercalcemia. Neck ultrasound and Tc-99m sestamibi found an enlarged lower right parathyroid gland. The gland was surgically removed, and an initial pathology report described atypical adenoma. Shortly afterward, she became pregnant again. During the second pregnancy, her calcium level was frequently controlled but was always in the normal range. Normocalcemia is explained by the specific physiology of pregnancy accompanied by hemodilution, hypoalbuminemia and maternal hypercalciuria (mediated by increased glomerular filtration). During lactation, calcium levels rose, and a new neck ultrasound showed a solitary mass in the area of prior surgery and an enlarged pretracheal lymph node. Fine needle aspiration of the solitary mass and node showed parathyroid carcinoma cells. The tumor mass was resected en bloc with the contiguous tissues and surrounding lymph nodes (pathology report; parathyroid carcinoma with metastases). Over the next five years, four consecutive surgeries were performed to remove malignant parathyroid tissue, lymph nodes and local metastases. Following the surgical procedures, no hypocalcemia was observed. More serious hypercalcemia recurred; the calcium level was difficult to control with a combination of pamidronate, cinacalcet and loop diuretic. No elements of multiple endocrine neoplasia were present.

Keywords: Parathyroid carcinoma, Hypercalcemia, Hyperparathyroidism, Pregnancy, Hyperemesis gravidarum

Core tip: Parathyroid carcinoma is the rarest endocrine malignancy; it is extremely uncommon in pregnancy. Hyperemesis gravidarum can mask the symptoms of hypercalcemia. The calcium level can be lower during pregnancy due to its specific physiology. This is a case report of a 24-year-old female patient with parathyroid carcinoma and two consecutive pregnancies with good outcomes in the postnatal period despite poor prognosis due to malignant disease. In five years, four consecutive surgeries were performed to remove malignant parathyroid tissue, lymph nodes and local metastases. Hypercalcemia was difficult to control with a combination of pamidronate, cinacalcet and loop diuretic. There were no elements of multiple endocrine neoplasia.