Multidisciplinary management of a neonate with oropharyngeal teratoma and bilateral cleft lip and palate: a rare congenital presentation

This case report describes a rare presentation of a male infant with a large congenital oropharyngeal teratoma, bilateral cleft lip and palate, and a low-type imperforate anus. The infant experienced airway obstruction at birth, necessitating immediate neonatal intensive care unit admission and surgical intervention. Imaging revealed craniofacial teratoma involvement, contributing to palatal fusion failure during embryonic development. Two major surgeries were performed: teratoma excision and anoplasty. Postoperatively, the infant faced respiratory distress, Klebsiella sepsis, and a urinary tract infection, all successfully managed. The coexistence of craniofacial teratoma with bilateral cleft lip and palate is exceptionally uncommon, highlighting the need for early diagnosis, multidisciplinary collaboration, and meticulous surgical planning to ensure optimal outcomes.

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Publication Details

Journal
Journal of Surgical Case Reports
Published
2025-04-29
DOI
https://doi.org/10.1093/jscr/rjaf293
Citations
1
Primary Topic
Teratomas and Epidermoid Cysts
Type
article
Field-Weighted Citation Impact
2.01
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Multidisciplinary management of a neonate with oropharyngeal teratoma and bilateral cleft lip and palate: a rare congenital presentation

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article

Multidisciplinary management of a neonate with oropharyngeal teratoma and bilateral cleft lip and palate: a rare congenital presentation

Obada Amro, Syakib Bakri, Ahmad Fasfoos, Safaa Heeh, Walaa Zighan, Ansam Manasrah, Radwan Abu Karsh, Mahran Abu Sirrieh
article en
1 citations

Abstract

This case report describes a rare presentation of a male infant with a large congenital oropharyngeal teratoma, bilateral cleft lip and palate, and a low-type imperforate anus. The infant experienced airway obstruction at birth, necessitating immediate neonatal intensive care unit admission and surgical intervention. Imaging revealed craniofacial teratoma involvement, contributing to palatal fusion failure during embryonic development. Two major surgeries were performed: teratoma excision and anoplasty. Postoperatively, the infant faced respiratory distress, Klebsiella sepsis, and a urinary tract infection, all successfully managed. The coexistence of craniofacial teratoma with bilateral cleft lip and palate is exceptionally uncommon, highlighting the need for early diagnosis, multidisciplinary collaboration, and meticulous surgical planning to ensure optimal outcomes.

Journal of Surgical Case ReportsVol. 2025(5)
Hebron University (PS)
Openalex Percentile: Top 16%
Teratomas and Epidermoid Cysts
2.01
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