A Papillary Thyroid Microcarcinoma Revealed by a Single Bone Lesion with No Poor Prognostic Factors

Objectives. Thyroid carcinomas incidence, in particular papillary variants, is increasing. These cancers are generally considered to have excellent prognosis, and papillary microcarcinomas are usually noninvasive. Many prognostic histopathology factors have been described to guide therapeutic decisi...

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Main Authors: Yann Godbert, Benedicte Henriques-Figueiredo, Anne-Laure Cazeau, Xavier Carrat, Marc Stegen, Isabelle Soubeyran, Francoise Bonichon
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Case Reports in Endocrinology
Online Access:http://dx.doi.org/10.1155/2013/719304
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author Yann Godbert
Benedicte Henriques-Figueiredo
Anne-Laure Cazeau
Xavier Carrat
Marc Stegen
Isabelle Soubeyran
Francoise Bonichon
author_facet Yann Godbert
Benedicte Henriques-Figueiredo
Anne-Laure Cazeau
Xavier Carrat
Marc Stegen
Isabelle Soubeyran
Francoise Bonichon
author_sort Yann Godbert
collection DOAJ
description Objectives. Thyroid carcinomas incidence, in particular papillary variants, is increasing. These cancers are generally considered to have excellent prognosis, and papillary microcarcinomas are usually noninvasive. Many prognostic histopathology factors have been described to guide therapeutic decisions. Most patients are treated with total thyroidectomy without radioiodine treatment or partial surgery. Case Summary. A 65-year-old man with no significant medical history presented with pain in the left chest wall that had been present for several months. A computed tomography (CT) found a large tissue mass of 4 cm responsible for lysis of the middle arch of the 4th rib on the left. It was a single lesion, highly hypermetabolic on the 18-FDG PET/CT. The histology analysis of the biopsy and surgical specimen favored an adenocarcinoma with immunostaining positive for TTF1 and thyroglobulin (Tg). The total thyroidectomy carried out subsequently revealed a 4 mm papillary microcarcinoma with vesicular architecture of the right lobe, well delimited and distant from the capsule without vascular embolisms. After two radioiodine treatments, the patient is in complete clinical, biological, and radiological remission. Conclusion. This extremely rare case of a singular bone metastasis revealing a papillary thyroid microcarcinoma illustrates the necessity of further research to better characterize the forms of papillary thyroid microcarcinomas with potentially poor prognosis.
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spelling doaj-art-d36275c6b9664a418974dbcd75d64bb02025-02-03T01:00:46ZengWileyCase Reports in Endocrinology2090-65012090-651X2013-01-01201310.1155/2013/719304719304A Papillary Thyroid Microcarcinoma Revealed by a Single Bone Lesion with No Poor Prognostic FactorsYann Godbert0Benedicte Henriques-Figueiredo1Anne-Laure Cazeau2Xavier Carrat3Marc Stegen4Isabelle Soubeyran5Francoise Bonichon6Department of Nuclear Medicine, Institut Bergonié, 229 Cours de L'Argonne, 33076 Bordeaux, FranceDepartment of Radiotherapy, Institut Bergonié, 229 Cours de L'Argonne, 33076 Bordeaux, FranceDepartment of Nuclear Medicine, Institut Bergonié, 229 Cours de L'Argonne, 33076 Bordeaux, FranceDepartment of Surgery, Institut Bergonié, 229 Cours de L'Argonne, 33076 Bordeaux, FranceDepartment of Nuclear Medicine, Centre Hospitalier de la Côte Basque, 13 avenue de l'interne Jacques Loëb, 64109 Bayonne, FranceDepartment of Pathology, Institut Bergonié, 229 Cours de L'Argonne, 33076 Bordeaux, FranceDepartment of Nuclear Medicine, Institut Bergonié, 229 Cours de L'Argonne, 33076 Bordeaux, FranceObjectives. Thyroid carcinomas incidence, in particular papillary variants, is increasing. These cancers are generally considered to have excellent prognosis, and papillary microcarcinomas are usually noninvasive. Many prognostic histopathology factors have been described to guide therapeutic decisions. Most patients are treated with total thyroidectomy without radioiodine treatment or partial surgery. Case Summary. A 65-year-old man with no significant medical history presented with pain in the left chest wall that had been present for several months. A computed tomography (CT) found a large tissue mass of 4 cm responsible for lysis of the middle arch of the 4th rib on the left. It was a single lesion, highly hypermetabolic on the 18-FDG PET/CT. The histology analysis of the biopsy and surgical specimen favored an adenocarcinoma with immunostaining positive for TTF1 and thyroglobulin (Tg). The total thyroidectomy carried out subsequently revealed a 4 mm papillary microcarcinoma with vesicular architecture of the right lobe, well delimited and distant from the capsule without vascular embolisms. After two radioiodine treatments, the patient is in complete clinical, biological, and radiological remission. Conclusion. This extremely rare case of a singular bone metastasis revealing a papillary thyroid microcarcinoma illustrates the necessity of further research to better characterize the forms of papillary thyroid microcarcinomas with potentially poor prognosis.http://dx.doi.org/10.1155/2013/719304
spellingShingle Yann Godbert
Benedicte Henriques-Figueiredo
Anne-Laure Cazeau
Xavier Carrat
Marc Stegen
Isabelle Soubeyran
Francoise Bonichon
A Papillary Thyroid Microcarcinoma Revealed by a Single Bone Lesion with No Poor Prognostic Factors
Case Reports in Endocrinology
title A Papillary Thyroid Microcarcinoma Revealed by a Single Bone Lesion with No Poor Prognostic Factors
title_full A Papillary Thyroid Microcarcinoma Revealed by a Single Bone Lesion with No Poor Prognostic Factors
title_fullStr A Papillary Thyroid Microcarcinoma Revealed by a Single Bone Lesion with No Poor Prognostic Factors
title_full_unstemmed A Papillary Thyroid Microcarcinoma Revealed by a Single Bone Lesion with No Poor Prognostic Factors
title_short A Papillary Thyroid Microcarcinoma Revealed by a Single Bone Lesion with No Poor Prognostic Factors
title_sort papillary thyroid microcarcinoma revealed by a single bone lesion with no poor prognostic factors
url http://dx.doi.org/10.1155/2013/719304
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