Congenital Maxillomandibular Synechia with Multiple Malformations in a Very-Low-Birth-Weight Infant: A Case Report.

IF 0.8 Q4 PEDIATRICS AJP Reports Pub Date : 2023-04-01 DOI:10.1055/a-2070-8590
Ryosuke Uchi, Mayu Koto, Atsushi Nakao, Miku Hosokawa, Toshiko Ukawa, Chisa Tsurisawa, Yoshiya Hisaeda, Shusuke Amagata
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Abstract

Abstract Congenital maxillomandibular synechia is a rare malformation that is characterized by a fusion of the maxilla and mandible. The fusion is fibrous or bony and prevents mouth opening, which causes difficulties in feeding and occasionally in breathing. Although extremely rare, neonatologists must understand the disease because it can be fatal and require emergency treatment after birth. We report the case of a very-low-birth-weight (VLBW) infant with congenital maxillomandibular synechia and other malformations, including cleft palate, syndactyly, and cryptorchidism. The patient presented with extremely limited mouth opening, and endotracheal intubation seemed impossible; fortunately, the patient did not have respiratory distress syndrome. The patient underwent surgical release of the fibrous bands on days 10 and 17, and good mouth opening was achieved. The patient was able to consume breast milk orally and was discharged home at a corrected gestational age of 1 month without recurrence of difficulty in mouth opening or any sequelae. This is the first reported case of a VLBW infant with congenital maxillomandibular synechia who required more complicated management of feeding, surgical intervention, and anesthesia.

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极低出生体重儿先天性上颌骨粘连合并多发性畸形1例。
摘要先天性上颌骨粘连是一种罕见的畸形,其特征是上颌骨和下颌骨融合。这种融合是纤维状或骨状的,可以防止张嘴,从而导致进食困难,偶尔也会导致呼吸困难。虽然极为罕见,但新生儿学家必须了解这种疾病,因为它可能是致命的,需要在出生后进行紧急治疗。我们报告一例极低出生体重(VLBW)婴儿与先天性上颌骨下颌粘连和其他畸形,包括腭裂,并指和隐睾。患者表现出极其有限的张嘴,气管插管似乎是不可能的;幸运的是,患者没有呼吸窘迫综合征。患者于第10天和第17天手术解除纤维带,口腔张开良好。患者能够口服母乳,并在1个月的正确胎龄出院,没有再次出现开口困难或任何后遗症。这是首例报道的VLBW婴儿患有先天性上颌骨粘连,需要更复杂的喂养、手术干预和麻醉管理。
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来源期刊
AJP Reports
AJP Reports PEDIATRICS-
CiteScore
2.20
自引率
0.00%
发文量
30
审稿时长
12 weeks
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