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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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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. |
format | Online Article Text |
id | pubmed-5053110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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