胎儿腹部囊性病变:诊断困境和预后挑战——两例中心系膜淋巴管瘤报告并文献复习

M. Rohilla, S. Siwatch, M. Malik, Tanuja Muthyala, R. Samujh, N. Kannan
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引用次数: 0

摘要

摘要胎儿肠系膜淋巴管瘤是一种罕见的先天性胎儿腹腔囊性畸形。因此,很少讨论产前检测、鉴别诊断、产前管理选择和关于这种情况的产后预后的父母咨询。我们报告两例产前检测胎儿囊性腹部肿块与腹部淋巴管瘤的临时诊断。出生后,其中一名新生儿出现肠梗阻的特征,需要手术干预。术中发现和组织病理学报告证实为肠系膜淋巴管瘤。另一名新生儿伴有左腰椎区皮下淋巴管扩张,左侧腹股沟疝,睾丸隐睾,出生后无症状,接受保守治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fetal Abdominal Cystic Lesion: A Diagnostic Dilemma and Prognostic Challenge-Report of Two Cases of Mesentric Lymphangioma with Review of Literature
Fetal mesentric lymphangioma, a congenital fetal abdominal cystic malformation has a rare occurrence. Antenatal detection, its differential diagnosis, prenatal management options and parental counseling regarding postnatal prognosis of such a case are thus rarely discussed. We report two cases of antenatally detected fetal cystic abdominal mass with a provisional diagnosis of abdominal lymphangioma. Postnatally one of the neonates developed features of intestinal obstruction and required surgical intervention. Intra-operative findings and histopathology report confirmed a mesentric lymphangioma. The other neonate had associated subcutaneous lymphangiectasia in left lumbar region, left sided inguinal hernia, undescended testes and was asymptomatic postnatally and managed conservatively.
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