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Hyperfuctioning insular thyroid carcinoma: A rare case report

INTRODUCTION: Insular carcinoma of thyroid (ICT) is a rare pattern of thyroid tumor. Being hyperfunctioning makes the condition rarer. Here we reported a case of ICT associated with hyperthyroidism. CASE REPORT: A 65-year-old female presented with neck mass for 4 years. She had symptoms of thyrotoxi...

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Detalles Bibliográficos
Autores principales: Salih, Abdulwahid M., Kakamad, F.H., Aube, Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053110/
https://www.ncbi.nlm.nih.gov/pubmed/27710874
http://dx.doi.org/10.1016/j.ijscr.2016.09.052
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author Salih, Abdulwahid M.
Kakamad, F.H.
Aube, Han
author_facet Salih, Abdulwahid M.
Kakamad, F.H.
Aube, Han
author_sort Salih, Abdulwahid M.
collection PubMed
description INTRODUCTION: Insular carcinoma of thyroid (ICT) is a rare pattern of thyroid tumor. Being hyperfunctioning makes the condition rarer. Here we reported a case of ICT associated with hyperthyroidism. CASE REPORT: A 65-year-old female presented with neck mass for 4 years. She had symptoms of thyrotoxicosis and received antithyroid treatment. She was referred for surgical management. She had multiple, non tender, mobile masses in the neck. Ultrasound showed midline multiple heterogenous mass lesions with multiple lymph nodes in right side of the neck largest one measuring 2 × 2 cm. The patient was prepared for total thyrodectomy with radical neck dissection. The result of histopathology confirmed unifocal, poorly differentiated ICT. The post operative course was uneventful. CONCLUSION: Insular carcinoma is a rare disease. It may present with long history of signs and symptoms of hyperthyroidism. Total thyroidectomy is the main line of treatment.
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spelling pubmed-50531102016-10-14 Hyperfuctioning insular thyroid carcinoma: A rare case report Salih, Abdulwahid M. Kakamad, F.H. Aube, Han Int J Surg Case Rep Case Report INTRODUCTION: Insular carcinoma of thyroid (ICT) is a rare pattern of thyroid tumor. Being hyperfunctioning makes the condition rarer. Here we reported a case of ICT associated with hyperthyroidism. CASE REPORT: A 65-year-old female presented with neck mass for 4 years. She had symptoms of thyrotoxicosis and received antithyroid treatment. She was referred for surgical management. She had multiple, non tender, mobile masses in the neck. Ultrasound showed midline multiple heterogenous mass lesions with multiple lymph nodes in right side of the neck largest one measuring 2 × 2 cm. The patient was prepared for total thyrodectomy with radical neck dissection. The result of histopathology confirmed unifocal, poorly differentiated ICT. The post operative course was uneventful. CONCLUSION: Insular carcinoma is a rare disease. It may present with long history of signs and symptoms of hyperthyroidism. Total thyroidectomy is the main line of treatment. Elsevier 2016-10-01 /pmc/articles/PMC5053110/ /pubmed/27710874 http://dx.doi.org/10.1016/j.ijscr.2016.09.052 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Salih, Abdulwahid M.
Kakamad, F.H.
Aube, Han
Hyperfuctioning insular thyroid carcinoma: A rare case report
title Hyperfuctioning insular thyroid carcinoma: A rare case report
title_full Hyperfuctioning insular thyroid carcinoma: A rare case report
title_fullStr Hyperfuctioning insular thyroid carcinoma: A rare case report
title_full_unstemmed Hyperfuctioning insular thyroid carcinoma: A rare case report
title_short Hyperfuctioning insular thyroid carcinoma: A rare case report
title_sort hyperfuctioning insular thyroid carcinoma: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5053110/
https://www.ncbi.nlm.nih.gov/pubmed/27710874
http://dx.doi.org/10.1016/j.ijscr.2016.09.052
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