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Abdominal Lymphangioma and Hemangioma in a Newborn

机译:腹部淋巴管瘤和新生儿的血管瘤

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Abdominal hemangiolymphangioma (HLA) in neonates is a rare condition that demands surgical intervention after a complete preoperative diagnostic approach. The differential diagnosis and the establishment of a therapeutic algorithm is a challenge, both for the neonatologists and the pediatric surgeons, because there is no consensus in the management of HLAs in infancy according to the literature. We report a rare case of abdominal HLA in a female newborn that was admitted to our pediatric surgery department with a prenatal diagnosis of an abdominal cystic tumor. After a thorough preoperative diagnostic approach, the neonate underwent an explorative laparotomy and lesion excision with simultaneous splenectomy due to the operative findings. The neonate had an uncomplicated postoperative period and is free of recurrence a year after. Only the pathology examination can reveal the HLA diagnosis. When a total surgical excision is evitable, a close follow-up follows an uncomplicated postoperative hospitalization.
机译:腹部血液摩托yoma(HLA)在新生儿中是一种罕见的病症,需要在完全术前诊断方法后提出手术干预。鉴别诊断和建立治疗算法是新生儿学家和儿科外科医生的挑战,因为根据文献,在婴儿期的HLA管理中没有共识。我们在雌性新生儿中举行了罕见的腹部HLA,该小儿外科部门被患有腹部囊肿的产前诊断。在彻底的术前诊断方法之后,新生儿因手术结果而接受了一种探索性剖腹手术和病变切除,同时脾切除。新生儿术后未复杂的术后,一年后没有复发。只有病理检查才能揭示HLA诊断。当总手术切除卓越时,紧密的随访术后术后不断复杂的住院治疗。

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