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Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report

INTRODUCTION AND IMPORTANCE: Congenital hypopharynx duplication cysts are a medical rarity; nevertheless, they offer an important differential diagnosis in neonatal dyspnea or feeding problems. CASE REPORT: Herein, we describe a case of delayed diagnosis but successful surgical removal of a large co...

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Autores principales: Baranski, Tomasz, Piroth, Werner, Seiffert, Peter, William, Marina, Tröbs, Ralf-Bodo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482990/
https://www.ncbi.nlm.nih.gov/pubmed/36055173
http://dx.doi.org/10.1016/j.ijscr.2022.107557
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author Baranski, Tomasz
Piroth, Werner
Seiffert, Peter
William, Marina
Tröbs, Ralf-Bodo
author_facet Baranski, Tomasz
Piroth, Werner
Seiffert, Peter
William, Marina
Tröbs, Ralf-Bodo
author_sort Baranski, Tomasz
collection PubMed
description INTRODUCTION AND IMPORTANCE: Congenital hypopharynx duplication cysts are a medical rarity; nevertheless, they offer an important differential diagnosis in neonatal dyspnea or feeding problems. CASE REPORT: Herein, we describe a case of delayed diagnosis but successful surgical removal of a large congenital hypopharynx cyst in a 4-month-old infant presenting with stridor. CLINICAL DISCUSSION: Early and proper diagnosis and surgical handling of hypopharynx cyst can help to achieve the best prognosis and outcome. CONCLUSION: We present the successful management of a newborn with a pharyngeal duplication cyst. In our case, the temporary postoperative laryngeal nerve palsy resolved within four weeks. Overstretching of recurrent laryngeal nerve might have caused this complication.
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spelling pubmed-94829902022-09-20 Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report Baranski, Tomasz Piroth, Werner Seiffert, Peter William, Marina Tröbs, Ralf-Bodo Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Congenital hypopharynx duplication cysts are a medical rarity; nevertheless, they offer an important differential diagnosis in neonatal dyspnea or feeding problems. CASE REPORT: Herein, we describe a case of delayed diagnosis but successful surgical removal of a large congenital hypopharynx cyst in a 4-month-old infant presenting with stridor. CLINICAL DISCUSSION: Early and proper diagnosis and surgical handling of hypopharynx cyst can help to achieve the best prognosis and outcome. CONCLUSION: We present the successful management of a newborn with a pharyngeal duplication cyst. In our case, the temporary postoperative laryngeal nerve palsy resolved within four weeks. Overstretching of recurrent laryngeal nerve might have caused this complication. Elsevier 2022-08-28 /pmc/articles/PMC9482990/ /pubmed/36055173 http://dx.doi.org/10.1016/j.ijscr.2022.107557 Text en © 2022 The Authors https://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
Baranski, Tomasz
Piroth, Werner
Seiffert, Peter
William, Marina
Tröbs, Ralf-Bodo
Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report
title Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report
title_full Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report
title_fullStr Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report
title_full_unstemmed Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report
title_short Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report
title_sort stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482990/
https://www.ncbi.nlm.nih.gov/pubmed/36055173
http://dx.doi.org/10.1016/j.ijscr.2022.107557
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