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Laryngeal Hamartoma in a Newborn

机译:新生儿喉部喉瘤

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We report an interesting case of a neonate presenting immediately after birth with respiratory distress, inspiratory stridor and difficult intubation. During operative microlaryngoscopy, a well-delineated papilloma like elongated supraglottic mass was seen. The patient underwent surgery, and the diagnosis was confirmed histologically. Biopsy revealed tissue compatible with hamartoma including blood vessel, nerve bundle and cartilage plate. The mass was removed by direct laryngoscopy. Neonatal laryngeal hamartomas are extremely rare. In general, an excellent prognosis is associated with these lesions, and the treatment of choice is endoscopic surgical excision. To our knowledge, this is the first description of a neonatal laryngeal hamartoma in Bangladesh.J Bangladesh Coll Phys Surg 2016; 34(3): 172-174
机译:我们报告了一个有趣的病例,新生儿出生后立即出现呼吸窘迫,吸气性喘鸣和插管困难。在术中显微喉镜检查中,发现了轮廓清晰的乳头状瘤,如细长声门上肿块。该患者接受了手术,并在组织学上明确了诊断。活检显示与错构瘤相容的组织,包括血管,神经束和软骨板。通过直接喉镜检查除去肿块。新生儿喉错构瘤极为罕见。通常,这些病变的预后良好,治疗的选择是内窥镜手术切除。据我们所知,这是孟加拉国首次描述的新生儿喉错构瘤。JBangladesh Coll Phys Surg 2016; 34(3):172-174

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