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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.
Afiliação
  • Baranski T; Department of Pediatric Surgery, Helios Clinic Duisburg, Germany. Electronic address: Tomasz.Baranski@helios-gesundheit.de.
  • Piroth W; Department of Radiology, Helios Clinic Wuppertal, Germany.
  • Seiffert P; Department of Pediatrics, Helios Clinic Duisburg, Germany.
  • William M; Department of Pathology, Helios Clinic Krefeld, Germany.
  • Tröbs RB; Department of Pediatric Surgery, Helios Clinic Duisburg, Germany.
Int J Surg Case Rep ; 98: 107557, 2022 Sep.
Article em En | MEDLINE | ID: mdl-36055173
ABSTRACT
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article