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首页> 外文期刊>Taiwanese journal of obstetrics and gynecology >Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review
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Giant fetal lymphangioma at chest wall and prognosis: Case report and literature review

机译:巨大胎儿胸壁淋巴管瘤及预后:病例报告及文献复习

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ObjectiveTo report a rare liveborn case with a giant, septated, chest wall lymphangioma that underwent prenatal expectation treatment.Case reportA case of giant fetal chest wall cystic lymphangioma was diagnosed prenatally at 19 weeks gestation. Expectation treatment was performed, carefully after prenatal counseling, ruling out other structural abnormalities. At 38 weeks gestation, ultrasound showed a multilocular, subcutaneous cystic mass of 12.3?cm?×?9.2?cm?×?11.0?cm located on the left chest wall and left upper arm. The tumor was surgically removed 4 days after birth, and no recurrence was observed in the following 18 months.ConclusionOur experience suggests that a large, septated fetal lymphangioma may still merit prenatal expectation treatment if there is no evidence for chromosomal and structural abnormality.
机译:目的报道一例罕见的,发生巨大,分隔的巨大胸壁淋巴管瘤的活产儿病例,并接受了产前预期治疗。病例报告在妊娠19周时被确诊为胎儿巨大的胸壁囊性淋巴管瘤。在产前咨询后仔细进行预期治疗,排除其他结构异常。妊娠38周时,超声显示位于左胸壁和左上臂的多眼皮下囊性肿块为12.3?cm?×?9.2?cm?×?11.0?cm。出生后4天通过手术切除了肿瘤,在随后的18个月中未观察到复发。结论我们的经验表明,如果没有染色体和结构异常的证据,较大的隔离胎儿淋巴管瘤可能仍值得进行产前预期治疗。

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