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Congenital crico-thyroid dysplasia: a comprehensive description.
Ayadi, Sirine; Hammami, Boutheina; Sallemi, Nesrine; Ben Ayed, Mariem; Chabchoub, Moez; Ben Mahfoudh, Kheireddine; Mnejja, Melek; Charfeddine, Ilhem.
Afiliación
  • Ayadi S; Faculty of Medicine of Sfax, Otolaryngology- Head and Neck Surgery Department and Research Laboratory LR23ES01, Habib Bourguiba Hospital, 3029, Sfax, Tunisia. sirine_ayadi@medecinesfax.org.
  • Hammami B; Faculty of Medicine of Sfax, Otolaryngology- Head and Neck Surgery Department and Research Laboratory LR23ES01, Habib Bourguiba Hospital, 3029, Sfax, Tunisia.
  • Sallemi N; Faculty of Medicine of Sfax, Otolaryngology- Head and Neck Surgery Department and Research Laboratory LR23ES01, Habib Bourguiba Hospital, 3029, Sfax, Tunisia.
  • Ben Ayed M; Faculty of Medicine of Sfax, Otolaryngology- Head and Neck Surgery Department and Research Laboratory LR23ES01, Habib Bourguiba Hospital, 3029, Sfax, Tunisia.
  • Chabchoub M; Faculty of Medicine of Sfax, Radiology Department, Habib Bourguiba Hospital, 3029, Sfax, Tunisia.
  • Ben Mahfoudh K; Faculty of Medicine of Sfax, Radiology Department, Habib Bourguiba Hospital, 3029, Sfax, Tunisia.
  • Mnejja M; Faculty of Medicine of Sfax, Otolaryngology- Head and Neck Surgery Department and Research Laboratory LR23ES01, Habib Bourguiba Hospital, 3029, Sfax, Tunisia.
  • Charfeddine I; Faculty of Medicine of Sfax, Otolaryngology- Head and Neck Surgery Department and Research Laboratory LR23ES01, Habib Bourguiba Hospital, 3029, Sfax, Tunisia.
Eur Arch Otorhinolaryngol ; 281(8): 4425-4428, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38795146
ABSTRACT

INTRODUCTION:

We describe a first case of human congenital crico-thyroid dysplasia associated to a right sided aortic arch and an aberrant subclavian artery. CASE PRESENTATION Our patient presented with a two-weeks history of acute dyspnea, and reported hoarseness since his childhood. An urgent tracheotomy was performed, followed by direct laryngoscopy. Endoscopic examination showed a deviation of the dorsoventral axis of the larynx, with an obstructive submucosal swelling the area of the right false cord and aryepiglottic fold. Computed tomography conducted the following day confirmed the crico-thyroid dysplasia, an infected laryngocele, and the presence of a right sided aortic arch and an aberrant subclavian artery.

CONCLUSION:

The embryological basis of these anomalies is attributed to congenital defects of the development of the fourth and sixth pharyngeal arches. To our knowledge, the congenital crico-thyroid dysplasia has not been previously reported in human. This case underscores the importance of recognizing anatomical variations in laryngeal cartilages, understanding their embryological origins, and potential associated malformations.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Arteria Subclavia Límite: Humans / Male Idioma: En Revista: Eur Arch Otorhinolaryngol Asunto de la revista: OTORRINOLARINGOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Túnez Pais de publicación: Alemania
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Arteria Subclavia Límite: Humans / Male Idioma: En Revista: Eur Arch Otorhinolaryngol Asunto de la revista: OTORRINOLARINGOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Túnez Pais de publicación: Alemania