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Thoracoscopic approach for massive thymic hyperplasia in an infant: Case report and literature review

INTRODUCTION: Massive thymic hyperplasia (MTH) is a very rare entity, with fewer than 20 cases reported in the literature in infancy. Most patients have respiratory symptoms and the enlarged thymus gland occupies one side of the thoracic cavity. Posterolateral thoracotomy or median sternotomy is the...

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Autores principales: Jiao, Jinghua, Yu, Jie, Chen, Chenghao, Chen, Tian, Zheng, Tiehua, He, Lejian, Zeng, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014623/
https://www.ncbi.nlm.nih.gov/pubmed/36937950
http://dx.doi.org/10.3389/fped.2023.1144384
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author Jiao, Jinghua
Yu, Jie
Chen, Chenghao
Chen, Tian
Zheng, Tiehua
He, Lejian
Zeng, Qi
author_facet Jiao, Jinghua
Yu, Jie
Chen, Chenghao
Chen, Tian
Zheng, Tiehua
He, Lejian
Zeng, Qi
author_sort Jiao, Jinghua
collection PubMed
description INTRODUCTION: Massive thymic hyperplasia (MTH) is a very rare entity, with fewer than 20 cases reported in the literature in infancy. Most patients have respiratory symptoms and the enlarged thymus gland occupies one side of the thoracic cavity. Posterolateral thoracotomy or median sternotomy is the main treatment for MTH in infants. We report a case of an infant with MTH in which the enlarged thymus occupied his bilateral thoracic cavity and he underwent video-assisted thoracoscopic surgery (VATS). In addition, we reviewed and summarized the relevant literature. CASE REPORT: A 4-month-old boy was admitted to the hospital with no apparent cause of dyspnea for 18 days, with cough and sputum. On examination, the patient was found to have cyanotic lips, diminished breath sounds in both lungs, and a positive three concave sign. There was no fever or ptosis. Preoperative imaging showed large soft tissue shadows in the bilateral thoracic cavity, with basic symmetry between the right and left sides. Tumor markers were within the normal range. Ultrasound-guided fine needle biopsy showed normal thymic structures with no evidence of malignancy. As his symptoms worsened, he eventually underwent unilateral thoracic approach video-assisted thoracoscopic exploratory surgery, during which a large mass occupying the bilateral thoracic cavity was removed in a separate block and part of the thymus in the left lobe was preserved. Pathological examination confirmed true thymic hyperplasia (TTH). No relevant complications occurred at the 2-month postoperative follow-up. CONCLUSION: In infants, MTH occupying the bilateral thoracic cavity can produce severe respiratory and circulatory symptoms due to occupying effects. Although a definitive preoperative diagnosis is sometimes difficult, after combining computed tomography (CT) and fine needle biopsy to exclude evidence of other malignancies, the enlarged thymus occupying the bilateral thoracic cavity can be resected via VATS. Whether the enlarged thymus occupies the bilateral thoracic cavity and the size of the thymus are not absolute contraindications to thoracoscopic surgery. The method is safe, feasible, and minimally invasive to the patient.
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spelling pubmed-100146232023-03-16 Thoracoscopic approach for massive thymic hyperplasia in an infant: Case report and literature review Jiao, Jinghua Yu, Jie Chen, Chenghao Chen, Tian Zheng, Tiehua He, Lejian Zeng, Qi Front Pediatr Pediatrics INTRODUCTION: Massive thymic hyperplasia (MTH) is a very rare entity, with fewer than 20 cases reported in the literature in infancy. Most patients have respiratory symptoms and the enlarged thymus gland occupies one side of the thoracic cavity. Posterolateral thoracotomy or median sternotomy is the main treatment for MTH in infants. We report a case of an infant with MTH in which the enlarged thymus occupied his bilateral thoracic cavity and he underwent video-assisted thoracoscopic surgery (VATS). In addition, we reviewed and summarized the relevant literature. CASE REPORT: A 4-month-old boy was admitted to the hospital with no apparent cause of dyspnea for 18 days, with cough and sputum. On examination, the patient was found to have cyanotic lips, diminished breath sounds in both lungs, and a positive three concave sign. There was no fever or ptosis. Preoperative imaging showed large soft tissue shadows in the bilateral thoracic cavity, with basic symmetry between the right and left sides. Tumor markers were within the normal range. Ultrasound-guided fine needle biopsy showed normal thymic structures with no evidence of malignancy. As his symptoms worsened, he eventually underwent unilateral thoracic approach video-assisted thoracoscopic exploratory surgery, during which a large mass occupying the bilateral thoracic cavity was removed in a separate block and part of the thymus in the left lobe was preserved. Pathological examination confirmed true thymic hyperplasia (TTH). No relevant complications occurred at the 2-month postoperative follow-up. CONCLUSION: In infants, MTH occupying the bilateral thoracic cavity can produce severe respiratory and circulatory symptoms due to occupying effects. Although a definitive preoperative diagnosis is sometimes difficult, after combining computed tomography (CT) and fine needle biopsy to exclude evidence of other malignancies, the enlarged thymus occupying the bilateral thoracic cavity can be resected via VATS. Whether the enlarged thymus occupies the bilateral thoracic cavity and the size of the thymus are not absolute contraindications to thoracoscopic surgery. The method is safe, feasible, and minimally invasive to the patient. Frontiers Media S.A. 2023-03-01 /pmc/articles/PMC10014623/ /pubmed/36937950 http://dx.doi.org/10.3389/fped.2023.1144384 Text en © 2023 Jiao, Yu, Chen, Chen, Zheng, He and Zeng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Jiao, Jinghua
Yu, Jie
Chen, Chenghao
Chen, Tian
Zheng, Tiehua
He, Lejian
Zeng, Qi
Thoracoscopic approach for massive thymic hyperplasia in an infant: Case report and literature review
title Thoracoscopic approach for massive thymic hyperplasia in an infant: Case report and literature review
title_full Thoracoscopic approach for massive thymic hyperplasia in an infant: Case report and literature review
title_fullStr Thoracoscopic approach for massive thymic hyperplasia in an infant: Case report and literature review
title_full_unstemmed Thoracoscopic approach for massive thymic hyperplasia in an infant: Case report and literature review
title_short Thoracoscopic approach for massive thymic hyperplasia in an infant: Case report and literature review
title_sort thoracoscopic approach for massive thymic hyperplasia in an infant: case report and literature review
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014623/
https://www.ncbi.nlm.nih.gov/pubmed/36937950
http://dx.doi.org/10.3389/fped.2023.1144384
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