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A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule

Parathyroid carcinoma (PC) is a rare endocrine malignancy. The tumor is mostly functioning, causing severe primary hyperparathyroidism, with high serum calcium and parathyroid hormone (PTH) levels. Nonfunctioning PC is extremely rare. We report a 50-year-old male patient who was referred to our Depa...

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Autores principales: Cetani, Filomena, Frustaci, Gianluca, Torregrossa, Liborio, Magno, Silvia, Basolo, Fulvio, Campomori, Alberto, Miccoli, Paolo, Marcocci, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563849/
https://www.ncbi.nlm.nih.gov/pubmed/26350418
http://dx.doi.org/10.1186/s12957-015-0672-9
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author Cetani, Filomena
Frustaci, Gianluca
Torregrossa, Liborio
Magno, Silvia
Basolo, Fulvio
Campomori, Alberto
Miccoli, Paolo
Marcocci, Claudio
author_facet Cetani, Filomena
Frustaci, Gianluca
Torregrossa, Liborio
Magno, Silvia
Basolo, Fulvio
Campomori, Alberto
Miccoli, Paolo
Marcocci, Claudio
author_sort Cetani, Filomena
collection PubMed
description Parathyroid carcinoma (PC) is a rare endocrine malignancy. The tumor is mostly functioning, causing severe primary hyperparathyroidism, with high serum calcium and parathyroid hormone (PTH) levels. Nonfunctioning PC is extremely rare. We report a 50-year-old male patient who was referred to our Department for a right thyroid nodule, incidentally detected on carotid Doppler ultrasound scan, with a fine-needle aspiration cytology showing a follicular lesion. At the time of our evaluation, neck ultrasound showed a 1.3 cm right hypoechoic thyroid nodule with irregular margins and the absence of enlarged bilateral cervical lymph nodes. Thyroid function tests were normal. Serum calcium was normal and plasma PTH slightly above the upper limit of the normal range. The patients underwent right lobectomy. The intraoperative frozen-section pathological examination raised the suspicion of a PC. Definitive histology showed a markedly irregular infiltrative growth of the tumor with invasion of the thyroid tissue and cervical soft tissues. Immunostaining for thyroglobulin was negative, whereas staining for chromogranin A and PTH showed a strong reactivity. Based on the microscopic findings and the immunohistochemical profile, the tumor was diagnosed as a PC. Postoperative serum calcium and phosphate levels were in the normal range. One month after surgery, serum calcium and PTH were normal. Neck ultrasound and total body computed tomography scan were negative for local and metastatic disease. Eight months later, serum calcium was normal and plasma PTH level remained around the upper limit of normal range. Neck ultrasound did not show any pathological lesions. This is the first case of a nonfunctioning sporadic PC misdiagnosed prior of surgery as a follicular thyroid nodule. The parathyroid nature of the neck lesion could not be suspected before surgery. Fine-needle aspiration cytology (FNAC) may fail to distinguish a parathyroid tumor from a benign thyroid nodule because at FNAC, parathyroid and thyroid lesions have some morphological similarities. Histological criteria are not always sufficient for the differential diagnosis, which can definitely be established using immunohistochemistry.
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spelling pubmed-45638492015-09-10 A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule Cetani, Filomena Frustaci, Gianluca Torregrossa, Liborio Magno, Silvia Basolo, Fulvio Campomori, Alberto Miccoli, Paolo Marcocci, Claudio World J Surg Oncol Case Report Parathyroid carcinoma (PC) is a rare endocrine malignancy. The tumor is mostly functioning, causing severe primary hyperparathyroidism, with high serum calcium and parathyroid hormone (PTH) levels. Nonfunctioning PC is extremely rare. We report a 50-year-old male patient who was referred to our Department for a right thyroid nodule, incidentally detected on carotid Doppler ultrasound scan, with a fine-needle aspiration cytology showing a follicular lesion. At the time of our evaluation, neck ultrasound showed a 1.3 cm right hypoechoic thyroid nodule with irregular margins and the absence of enlarged bilateral cervical lymph nodes. Thyroid function tests were normal. Serum calcium was normal and plasma PTH slightly above the upper limit of the normal range. The patients underwent right lobectomy. The intraoperative frozen-section pathological examination raised the suspicion of a PC. Definitive histology showed a markedly irregular infiltrative growth of the tumor with invasion of the thyroid tissue and cervical soft tissues. Immunostaining for thyroglobulin was negative, whereas staining for chromogranin A and PTH showed a strong reactivity. Based on the microscopic findings and the immunohistochemical profile, the tumor was diagnosed as a PC. Postoperative serum calcium and phosphate levels were in the normal range. One month after surgery, serum calcium and PTH were normal. Neck ultrasound and total body computed tomography scan were negative for local and metastatic disease. Eight months later, serum calcium was normal and plasma PTH level remained around the upper limit of normal range. Neck ultrasound did not show any pathological lesions. This is the first case of a nonfunctioning sporadic PC misdiagnosed prior of surgery as a follicular thyroid nodule. The parathyroid nature of the neck lesion could not be suspected before surgery. Fine-needle aspiration cytology (FNAC) may fail to distinguish a parathyroid tumor from a benign thyroid nodule because at FNAC, parathyroid and thyroid lesions have some morphological similarities. Histological criteria are not always sufficient for the differential diagnosis, which can definitely be established using immunohistochemistry. BioMed Central 2015-09-08 /pmc/articles/PMC4563849/ /pubmed/26350418 http://dx.doi.org/10.1186/s12957-015-0672-9 Text en © Cetani et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Cetani, Filomena
Frustaci, Gianluca
Torregrossa, Liborio
Magno, Silvia
Basolo, Fulvio
Campomori, Alberto
Miccoli, Paolo
Marcocci, Claudio
A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule
title A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule
title_full A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule
title_fullStr A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule
title_full_unstemmed A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule
title_short A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule
title_sort nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563849/
https://www.ncbi.nlm.nih.gov/pubmed/26350418
http://dx.doi.org/10.1186/s12957-015-0672-9
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