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首页> 外文期刊>Annals of Medicine and Surgery >Serious neonatal airway obstruction with massive congenital sublingual ranula and contralateral occurrence
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Serious neonatal airway obstruction with massive congenital sublingual ranula and contralateral occurrence

机译:严重的新生儿气道阻塞,伴有先天性大舌下肉芽和对侧发生

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Background Congenital ranulas seldom occur, with bilateral presentation and prenatal diagnosis reported very rarely. We believe this is the first reported case of a neonate with a antenally diagnosed massive congenital ranula, who went on to develop a non-contiguous contralateral ranula, both contributing to obstruction in a complex paediatric airway. Case report A female neonate was born to a non-primagravid mother via a planned elective caesarean section due to a lower facial defect and oral cyst. Antenatal aspiration of the pseudocyst was performed under ultrasound guidance with limited success. In the immediate post-natal period a poor airway was observed and the cyst was subsequently marsupialised. With the development of macroglossia secondary to oedema and tongue base collapse the airway was secured through surgical tracheostomy. A subsequent ultrasound scan revealed the presence of a second solitary cystic mass on the contralateral side. After careful excision of the contralateral pseudocyst, tongue function improved, with the resolution of a safe airway which permitted successful decannulation. A planned definitive procedure antenatally did not result in the anticipated improvement in function. However the subsequent development of a second non-contiguous pseudocyst and further surgical management resulted in a safe airway, improved masticator function and the ability to thrive. Conclusions The prenatal diagnosis of congenital ranulas have been seldom reported, with no reported cases of contralateral occurrence and airway obstruction from an intraoral ranula. This rare case highlights the need for a well considered contingency plan when surgery is required for a neonatal airway at risk. Highlights ? A well considered plan is required when a neonatal surgical airway is required. ? Intra-oral ranulas can be initially managed with marsupialisation or cyst excision. ? Sublingual gland excision is more reliable but associated with higher risk. ? Sublingual gland excision should be reserved for recalcitrant cysts.
机译:背景很少发生先天性红斑,双侧表现和产前诊断很少。我们认为,这是首次报告的新生儿,其诊断为先天性大块肉芽肿,随后发展为不连续的对侧肉芽肿,均导致复杂的儿科气道阻塞。病例报告一名女性新生儿因面部缺损和口腔囊肿而通过计划内的剖腹产手术出生于一名非初生母亲。在超声引导下进行假性囊肿的产前抽吸术,但效果有限。在出生后即刻,观察到气道不畅,随后囊肿被囊化。随着继发于水肿和舌根塌陷的大舌症的发展,通过外科气管切开术确保了气道的安全。随后的超声扫描显示对侧有第二个孤立性囊性肿块。仔细切除对侧假性囊肿后,舌头功能得到改善,并通过安全气道得以解决,从而成功实现了脱位。产前计划的确定性手术并未导致预期的功能改善。然而,随后的第二个非连续假性囊肿的发展以及进一步的外科手术处理导致了安全的呼吸道,改善了咀嚼器功能和壮成长的能力。结论鲜有先天性先天性胎膜炎的产前诊断报道,未见有对侧发生和口腔内气道阻塞的病例。这种罕见的病例凸显了当有风险的新生儿气道需要手术时,需要制定周密的应急计划。强调 ?当需要新生儿手术气道时,需要周密的计划。 ?可以通过有袋化或囊肿切除术初步治疗口内肉芽。 ?舌下腺切除术更可靠,但风险更高。 ?舌下腺切除术应保留顽固性囊肿。

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