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首页> 外文期刊>Taiwanese journal of obstetrics and gynecology >Cavernous lymphangioma of fetal thigh
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Cavernous lymphangioma of fetal thigh

机译:胎儿大腿海绵状淋巴管瘤

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A 35-year-old woman was referred to our institution at 19 weeks' gestation because a mass located at the right fetal thigh was noted, reporting with a 46,XX karyotype of cultured amniotic cells. Prenatal ultrasound examinations revealed a 73 mm × 47 mm × 35 mm irregular multiseptated cystic mass involving the whole right fetal thigh with no obvious blood flow visualized using color Doppler images (Fig. 1A and B). The remaining ultrasound images for the female fetus, placenta, and amniotic fluid were unremarkable. Given a tentative diagnosis of lymphangioma and uncertain postnatal prognosis regarding functional and aesthetic impairments after treatment, the patient made a decision to terminate the pregnancy. Postmortem photographs were compatible with the prenatal three-dimensional ultrasound images (Fig. 2A and B). The pathologic reports confirmed an isolated unencapsulated cavernous lymphangioma involving the dermis and subcutaneous layers and composed of multiple dilated thin-wall lymphatic vessels filled with proteinaceous fluid (Fig. 3).
机译:一名19岁的孕妇在妊娠19周时被转诊到我们的机构,原因是发现其位于胎儿右大腿的肿块,并报告有46,XX核型的培养羊水。产前超声检查发现73毫米×47毫米×35毫米不规则的多囊性囊性肿块,累及整个右胎儿大腿,使用彩色多普勒图像未见明显的血流(图1A和B)。女性胎儿,胎盘和羊水的其余超声图像不明显。鉴于对淋巴管瘤的初步诊断,以及治疗后功能和美观受损的不确定产后预后,患者决定终止妊娠。验尸照片与产前三维超声图像兼容(图2A和B)。病理报告证实了一个孤立的未包囊的海绵状淋巴管瘤,累及真皮和皮下层,由多个充满蛋白质液的扩张的薄壁淋巴管组成(图3)。

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