Cargando…

Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review

Gestational primary hyperparathyroidism (GPHPT) is a rare condition with fewer than 200 cases reported. We present the case of a 21-year-old woman who presented at 10 weeks’ gestation with severe hypercalcemia. Laboratory investigation was consistent with primary hyperparathyroidism. Neck ultrasound...

Descripción completa

Detalles Bibliográficos
Autores principales: Horton, William B., Stumpf, Meaghan M., Coppock, Joseph D., Lancaster, Luke, Dalkin, Alan C., Liu, Zhenqi, Chisholm, Christian A., Smith, Philip W., Kirk, Susan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686630/
https://www.ncbi.nlm.nih.gov/pubmed/29264569
http://dx.doi.org/10.1210/js.2017-00172
_version_ 1783278811141373952
author Horton, William B.
Stumpf, Meaghan M.
Coppock, Joseph D.
Lancaster, Luke
Dalkin, Alan C.
Liu, Zhenqi
Chisholm, Christian A.
Smith, Philip W.
Kirk, Susan E.
author_facet Horton, William B.
Stumpf, Meaghan M.
Coppock, Joseph D.
Lancaster, Luke
Dalkin, Alan C.
Liu, Zhenqi
Chisholm, Christian A.
Smith, Philip W.
Kirk, Susan E.
author_sort Horton, William B.
collection PubMed
description Gestational primary hyperparathyroidism (GPHPT) is a rare condition with fewer than 200 cases reported. We present the case of a 21-year-old woman who presented at 10 weeks’ gestation with severe hypercalcemia. Laboratory investigation was consistent with primary hyperparathyroidism. Neck ultrasound did not reveal any parathyroid enlargement. Due to the persistence of severe hypercalcemia, she was treated with 4 weeks of cinacalcet therapy, which was poorly tolerated due to nausea and vomiting. At 14 weeks’ gestation, she underwent neck exploration with right lower, left upper, and partial right upper parathyroid gland excision. Intra- and postoperative parathyroid hormone (PTH) and calcium levels remained elevated. After a thorough discussion of risks/benefits, the patient requested further treatment. A parathyroid sestamibi scan (PSS) revealed an ectopic adenoma in the left mediastinum. The adenoma was removed via video-assisted thorascopic parathyroidectomy with intraoperative PTH declining to nearly undetectable levels. She ultimately delivered a physically and developmentally normal infant at 37 weeks’ gestation. Appropriate treatment of severe GPHPT may prevent the maternal and fetal complications of hypercalcemia. This case, in which cinacalcet therapy and PSS were used, adds to the body of literature regarding treatment of severe GPHPT.
format Online
Article
Text
id pubmed-5686630
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Endocrine Society
record_format MEDLINE/PubMed
spelling pubmed-56866302017-12-20 Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review Horton, William B. Stumpf, Meaghan M. Coppock, Joseph D. Lancaster, Luke Dalkin, Alan C. Liu, Zhenqi Chisholm, Christian A. Smith, Philip W. Kirk, Susan E. J Endocr Soc Case Reports Gestational primary hyperparathyroidism (GPHPT) is a rare condition with fewer than 200 cases reported. We present the case of a 21-year-old woman who presented at 10 weeks’ gestation with severe hypercalcemia. Laboratory investigation was consistent with primary hyperparathyroidism. Neck ultrasound did not reveal any parathyroid enlargement. Due to the persistence of severe hypercalcemia, she was treated with 4 weeks of cinacalcet therapy, which was poorly tolerated due to nausea and vomiting. At 14 weeks’ gestation, she underwent neck exploration with right lower, left upper, and partial right upper parathyroid gland excision. Intra- and postoperative parathyroid hormone (PTH) and calcium levels remained elevated. After a thorough discussion of risks/benefits, the patient requested further treatment. A parathyroid sestamibi scan (PSS) revealed an ectopic adenoma in the left mediastinum. The adenoma was removed via video-assisted thorascopic parathyroidectomy with intraoperative PTH declining to nearly undetectable levels. She ultimately delivered a physically and developmentally normal infant at 37 weeks’ gestation. Appropriate treatment of severe GPHPT may prevent the maternal and fetal complications of hypercalcemia. This case, in which cinacalcet therapy and PSS were used, adds to the body of literature regarding treatment of severe GPHPT. Endocrine Society 2017-06-30 /pmc/articles/PMC5686630/ /pubmed/29264569 http://dx.doi.org/10.1210/js.2017-00172 Text en Copyright © 2017 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Reports
Horton, William B.
Stumpf, Meaghan M.
Coppock, Joseph D.
Lancaster, Luke
Dalkin, Alan C.
Liu, Zhenqi
Chisholm, Christian A.
Smith, Philip W.
Kirk, Susan E.
Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review
title Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review
title_full Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review
title_fullStr Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review
title_full_unstemmed Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review
title_short Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review
title_sort gestational primary hyperparathyroidism due to ectopic parathyroid adenoma: case report and literature review
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686630/
https://www.ncbi.nlm.nih.gov/pubmed/29264569
http://dx.doi.org/10.1210/js.2017-00172
work_keys_str_mv AT hortonwilliamb gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview
AT stumpfmeaghanm gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview
AT coppockjosephd gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview
AT lancasterluke gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview
AT dalkinalanc gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview
AT liuzhenqi gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview
AT chisholmchristiana gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview
AT smithphilipw gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview
AT kirksusane gestationalprimaryhyperparathyroidismduetoectopicparathyroidadenomacasereportandliteraturereview