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首页> 外文期刊>International Journal of Reproduction, Contraception, Obstetrics and Gynecology >Bilateral ovarian cystic lymphangioma with chylous ascitis in pregnancy - a rare case report with review
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Bilateral ovarian cystic lymphangioma with chylous ascitis in pregnancy - a rare case report with review

机译:妊娠合并乳糜性腹水的双侧卵巢囊性淋巴管瘤-罕见病例报告

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摘要

Bilateral lymphangioma of the ovary being an extremely rare lesion, with chylous ascites and full term pregnancy, this is the first ever case in the world to be reported. Chylous ascites with pregnancy only 5 cases have been reported earlier. And above all, only 20 cases of ovarian lymphangioma are reported in the literature so far. Lymphangioma is usually asymptomatic and unilateral, presenting as an incidental finding during routine gynaecologic procedures. It is made up of aggregates of lymphatic spaces in ovarian stroma and the endothelial cells lining these spaces. The main differential diagnosis is an adenomatoid tumour which can be differentiated from the lymphangioma by immunohistochemical studies. We report this rare lesion in a case of 28 years old primigravida with 37 weeks of gestation with pregnancy induced hypertension with acute distension of abdomen with respiratory distress.
机译:卵巢双侧淋巴管瘤是一种极为罕见的病变,有乳腺腹水和足月妊娠,这是世界上首例报道的病例。早产儿有乳糜性腹水5例。最重要的是,迄今为止,文献中仅报道了20例卵巢淋巴管瘤。淋巴管瘤通常是无症状的和单侧的,表现为常规妇科手术中的偶然发现。它是由卵巢基质中的淋巴间隙和聚集在这些间隙中的内皮细胞组成的。主要的鉴别诊断是腺瘤样肿瘤,可通过免疫组织化学研究将其与淋巴管瘤区分开。我们报告了这种罕见的病变,该病例发生在妊娠37周,妊娠引起的高血压,腹部急性扩张并伴呼吸窘迫的28岁初孕期。

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