An Unusual Simultaneous Existence of Parathyroid Carcinoma and Papillary Thyroid Carcinoma: Case Report and Review of Literature

Synchronous parathyroid and papillary thyroid carcinoma are extremely rare. To our knowledge, only 15 cases have been reported in the last four decades. We describe a 50-year-old female without significant past medical or family history and no previous trauma presented with left heel pain that promp...

Full description

Saved in:
Bibliographic Details
Main Authors: César Ernesto Lam-Chung, Diana Lizbeth Rodríguez-Orihuela, Jazmín De Anda González, Armando Gamboa-Domínguez
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Case Reports in Endocrinology
Online Access:http://dx.doi.org/10.1155/2020/2128093
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849413759776325632
author César Ernesto Lam-Chung
Diana Lizbeth Rodríguez-Orihuela
Jazmín De Anda González
Armando Gamboa-Domínguez
author_facet César Ernesto Lam-Chung
Diana Lizbeth Rodríguez-Orihuela
Jazmín De Anda González
Armando Gamboa-Domínguez
author_sort César Ernesto Lam-Chung
collection DOAJ
description Synchronous parathyroid and papillary thyroid carcinoma are extremely rare. To our knowledge, only 15 cases have been reported in the last four decades. We describe a 50-year-old female without significant past medical or family history and no previous trauma presented with left heel pain that prompted her to seek medical attention. Physical examination was notable for a painless nodule at the left thyroid lobe. Laboratory evaluation showed a serum calcium level of 14.3 mg/dL (8.6–10.3 mg/dL) and intact parathyroid hormone level of 1160 pg/mL (12–88 pg/mL). 99Tc-sestamibi dual-phase with single-photon emission computed tomography fused images showed increased uptake at the left-sided inferior parathyroid gland. Neck ultrasound showed a 1.4 cm heterogeneous nodule in the middle-third of the left thyroid gland and a solitary 1.9 cm vascularized and hypoechoic oval nodule that was considered likely to represent a parathyroid adenoma. Due to its clinical context (severe hypercalcemia and very high levels of PTH), parathyroid carcinoma (PC) was suspected although imaging studies were not characteristic. The patient underwent en bloc resection of the parathyroid mass and left thyroid lobe and central neck compartment dissection. Pathology analysis revealed classical papillary thyroid carcinoma of classical subtype and parathyroid carcinoma. Immunohistochemical staining was positive for cyclidin D1 and negative for parafibromin. High clinical suspicion is required for parathyroid carcinoma diagnosis in the presence of very high level of parathyroid hormone, marked hypercalcemia, and the existence of any thyroid nodule should be approached and the coexistence of other carcinomas should be considered.
format Article
id doaj-art-704afeb3e39d4d9d8b9c87ee52073983
institution Kabale University
issn 2090-6501
2090-651X
language English
publishDate 2020-01-01
publisher Wiley
record_format Article
series Case Reports in Endocrinology
spelling doaj-art-704afeb3e39d4d9d8b9c87ee520739832025-08-20T03:34:01ZengWileyCase Reports in Endocrinology2090-65012090-651X2020-01-01202010.1155/2020/21280932128093An Unusual Simultaneous Existence of Parathyroid Carcinoma and Papillary Thyroid Carcinoma: Case Report and Review of LiteratureCésar Ernesto Lam-Chung0Diana Lizbeth Rodríguez-Orihuela1Jazmín De Anda González2Armando Gamboa-Domínguez3Department of Endocrinology and Metabolism, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga 15, Sección XVI, Tlalpan, México City 14000, MexicoDepartment of Pathology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga 15, Sección XVI, Tlalpan, México City 14000, MexicoDepartment of Pathology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga 15, Sección XVI, Tlalpan, México City 14000, MexicoDepartment of Pathology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga 15, Sección XVI, Tlalpan, México City 14000, MexicoSynchronous parathyroid and papillary thyroid carcinoma are extremely rare. To our knowledge, only 15 cases have been reported in the last four decades. We describe a 50-year-old female without significant past medical or family history and no previous trauma presented with left heel pain that prompted her to seek medical attention. Physical examination was notable for a painless nodule at the left thyroid lobe. Laboratory evaluation showed a serum calcium level of 14.3 mg/dL (8.6–10.3 mg/dL) and intact parathyroid hormone level of 1160 pg/mL (12–88 pg/mL). 99Tc-sestamibi dual-phase with single-photon emission computed tomography fused images showed increased uptake at the left-sided inferior parathyroid gland. Neck ultrasound showed a 1.4 cm heterogeneous nodule in the middle-third of the left thyroid gland and a solitary 1.9 cm vascularized and hypoechoic oval nodule that was considered likely to represent a parathyroid adenoma. Due to its clinical context (severe hypercalcemia and very high levels of PTH), parathyroid carcinoma (PC) was suspected although imaging studies were not characteristic. The patient underwent en bloc resection of the parathyroid mass and left thyroid lobe and central neck compartment dissection. Pathology analysis revealed classical papillary thyroid carcinoma of classical subtype and parathyroid carcinoma. Immunohistochemical staining was positive for cyclidin D1 and negative for parafibromin. High clinical suspicion is required for parathyroid carcinoma diagnosis in the presence of very high level of parathyroid hormone, marked hypercalcemia, and the existence of any thyroid nodule should be approached and the coexistence of other carcinomas should be considered.http://dx.doi.org/10.1155/2020/2128093
spellingShingle César Ernesto Lam-Chung
Diana Lizbeth Rodríguez-Orihuela
Jazmín De Anda González
Armando Gamboa-Domínguez
An Unusual Simultaneous Existence of Parathyroid Carcinoma and Papillary Thyroid Carcinoma: Case Report and Review of Literature
Case Reports in Endocrinology
title An Unusual Simultaneous Existence of Parathyroid Carcinoma and Papillary Thyroid Carcinoma: Case Report and Review of Literature
title_full An Unusual Simultaneous Existence of Parathyroid Carcinoma and Papillary Thyroid Carcinoma: Case Report and Review of Literature
title_fullStr An Unusual Simultaneous Existence of Parathyroid Carcinoma and Papillary Thyroid Carcinoma: Case Report and Review of Literature
title_full_unstemmed An Unusual Simultaneous Existence of Parathyroid Carcinoma and Papillary Thyroid Carcinoma: Case Report and Review of Literature
title_short An Unusual Simultaneous Existence of Parathyroid Carcinoma and Papillary Thyroid Carcinoma: Case Report and Review of Literature
title_sort unusual simultaneous existence of parathyroid carcinoma and papillary thyroid carcinoma case report and review of literature
url http://dx.doi.org/10.1155/2020/2128093
work_keys_str_mv AT cesarernestolamchung anunusualsimultaneousexistenceofparathyroidcarcinomaandpapillarythyroidcarcinomacasereportandreviewofliterature
AT dianalizbethrodriguezorihuela anunusualsimultaneousexistenceofparathyroidcarcinomaandpapillarythyroidcarcinomacasereportandreviewofliterature
AT jazmindeandagonzalez anunusualsimultaneousexistenceofparathyroidcarcinomaandpapillarythyroidcarcinomacasereportandreviewofliterature
AT armandogamboadominguez anunusualsimultaneousexistenceofparathyroidcarcinomaandpapillarythyroidcarcinomacasereportandreviewofliterature
AT cesarernestolamchung unusualsimultaneousexistenceofparathyroidcarcinomaandpapillarythyroidcarcinomacasereportandreviewofliterature
AT dianalizbethrodriguezorihuela unusualsimultaneousexistenceofparathyroidcarcinomaandpapillarythyroidcarcinomacasereportandreviewofliterature
AT jazmindeandagonzalez unusualsimultaneousexistenceofparathyroidcarcinomaandpapillarythyroidcarcinomacasereportandreviewofliterature
AT armandogamboadominguez unusualsimultaneousexistenceofparathyroidcarcinomaandpapillarythyroidcarcinomacasereportandreviewofliterature