Right-Sided Fourth Branchial Cleft Cyst in a Neonate: A Case Report and Literature Review.

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL Cureus Pub Date : 2024-10-16 eCollection Date: 2024-10-01 DOI:10.7759/cureus.71624
Osama Qumsieh, Maram Heeh, Anas Abukhalaf, Kenana Altel, Fatima Amer, Sajeda Nawajaa
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Abstract

Anomalies of the fourth branchial cleft are exceedingly uncommon, presenting with a diverse array of clinical manifestations. The majority of branchial cleft anomalies, approximately 95%, are of the second type, with a mere 2% attributed to the fourth type. The latter is notably more prevalent on the left side, with reports indicating an 85% incidence. Herein, we report the case of a neonate presenting with a right-sided fourth branchial cleft cyst, which manifested at birth and subsequently underwent progressive enlargement, resulting in airway and esophageal compromise. The management strategy involved surgical excision, and the definitive diagnosis was established through histopathological examination, underscoring the rarity and diagnostic challenge of this form of branchial cyst.

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新生儿右侧第四支裂囊肿:病例报告与文献综述
第四腮裂异常极为罕见,临床表现多种多样。大多数支裂畸形(约 95%)属于第二种类型,只有 2% 属于第四种类型。后者在左侧更为常见,有报告显示其发生率为 85%。在此,我们报告了一例患有右侧第四膈裂囊肿的新生儿,该囊肿在出生时就已出现,随后逐渐增大,导致气道和食道受损。治疗策略包括手术切除,并通过组织病理学检查确定了最终诊断,凸显了这种形式的腮腺囊肿的罕见性和诊断难度。
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