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Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma

Adult cases of congenital arteriovenous malformation (AVM) of the mediastinum are extremely rare, and because of their varied clinical presentations, they pose a diagnostic challenge. There is no reported association of pulmonary AVM and papillary thyroid carcinoma. We describe a 38-year-old female...

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Autores principales: Palaniswamy, Shanmuga Sundaram, Subramanyam, Padma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905278/
https://www.ncbi.nlm.nih.gov/pubmed/33642758
http://dx.doi.org/10.4103/ijnm.IJNM_75_20
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author Palaniswamy, Shanmuga Sundaram
Subramanyam, Padma
author_facet Palaniswamy, Shanmuga Sundaram
Subramanyam, Padma
author_sort Palaniswamy, Shanmuga Sundaram
collection PubMed
description Adult cases of congenital arteriovenous malformation (AVM) of the mediastinum are extremely rare, and because of their varied clinical presentations, they pose a diagnostic challenge. There is no reported association of pulmonary AVM and papillary thyroid carcinoma. We describe a 38-year-old female with a large right lung AVM, multinodular goiter, and high serum thyroglobulin (Tg) with papillary thyroid carcinoma. The lung mass was believed to represent a pulmonary metastatic deposit due to high Tg value. Whole body I-131 scan and FDG PETMR imaging were performed as part of the workup.
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spelling pubmed-79052782021-02-26 Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma Palaniswamy, Shanmuga Sundaram Subramanyam, Padma Indian J Nucl Med Case Report Adult cases of congenital arteriovenous malformation (AVM) of the mediastinum are extremely rare, and because of their varied clinical presentations, they pose a diagnostic challenge. There is no reported association of pulmonary AVM and papillary thyroid carcinoma. We describe a 38-year-old female with a large right lung AVM, multinodular goiter, and high serum thyroglobulin (Tg) with papillary thyroid carcinoma. The lung mass was believed to represent a pulmonary metastatic deposit due to high Tg value. Whole body I-131 scan and FDG PETMR imaging were performed as part of the workup. Wolters Kluwer - Medknow 2020 2020-10-21 /pmc/articles/PMC7905278/ /pubmed/33642758 http://dx.doi.org/10.4103/ijnm.IJNM_75_20 Text en Copyright: © 2020 Indian Journal of Nuclear Medicine http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Palaniswamy, Shanmuga Sundaram
Subramanyam, Padma
Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma
title Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma
title_full Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma
title_fullStr Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma
title_full_unstemmed Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma
title_short Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma
title_sort asymptomatic large pulmonary arteriovenous malformation masquerading as a metastatic deposit in a patient with papillary thyroid carcinoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905278/
https://www.ncbi.nlm.nih.gov/pubmed/33642758
http://dx.doi.org/10.4103/ijnm.IJNM_75_20
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