首页> 外文期刊>Journal of medical ultrasonics: official journal of the Japan Society of Ultrasonics in Medicine >Morphological changes observed via fetal ultrasound in prenatally diagnosed and isolated congenital lymphangiomas: Three case reports
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Morphological changes observed via fetal ultrasound in prenatally diagnosed and isolated congenital lymphangiomas: Three case reports

机译:通过胎儿超声在产前诊断和孤立的先天性淋巴管瘤中观察到的形态学变化:三例报告

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摘要

We illustrate three cases of isolated congenital lymphangioma (CL). Fetal ultrasound (US) demonstrated uniloculated cystic masses that changed to multiloculated, subcutaneous, hypoechoic, avascular cystic masses with thin septations without solid components. Case 1: CL of the right forearm; Case 2: CL of the right hypochondrium; and Case 3: CL of the left upper posterior back. Postnatal US detected multiloculated, subcutaneous, hypoechoic, avascular cystic masses with thin septations without solid components or invasive developments. We prenatally and postnatally diagnosed them as isolated CL cases due to focal, soft, bulging masses with unclear margins. Due to our correct diagnosis and precise evaluation of sizes and locations, no perinatal complications occurred. In this case series, uniloculated features changed to multiloculated features and the largest macrocyst size decreased, whereas the sizes of the smaller microcysts increased. These morphological changes observed via fetal US represent intermittent CL growing processes.
机译:我们说明了三例孤立的先天性淋巴管瘤(CL)。胎儿超声检查(美国)显示单位囊性肿块变为多处,皮下,低回声,无血管的囊性肿块,隔膜较薄,无固体成分。病例1:右前臂CL案例2:右下软骨CL案例3:左上后背部的CL。产后US检测到多处,皮下,低回声,无血管的囊性肿物,隔膜稀薄,无固体成分或侵袭性发展。我们在产前和产后将其诊断为孤立的CL病例,原因是病灶,软,隆起的肿块,边缘不清楚。由于我们的正确诊断和对大小和位置的准确评估,因此未发生围产期并发症。在这种情况下,单位特征变为多位特征,最大的大囊肿大小减小,而较小的微囊肿大小增加。通过胎儿超声观察到的这些形态变化代表了间歇性CL生长过程。

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