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Breus’ Mole Associated with Hereditary Thrombophilia in A Teenage Girl

机译:布鲁斯的痣与少女的遗传性血栓形成有关

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Breus’ mole is a rare event and it is most often found in the placenta of stillborn fetuses. It may occur in?patients with disorders of circulation, complex heart disease, hypertension, diabetes and anticoagulation?therapy. A 17 year old women with no previous gravida, was admitted to our clinic with intermittent vaginal bleeding and lower abdominal pain after 2 months amenorrhea. On admission, her general condition?was normal and biochemical profiles were within normal ranges. Ultrasonography showed an enlarged?uterus with hyper/hypoechogenic vesicular areas. Serum β-human chorionic gonadotropin (HCG)?was tested as 33096 U/ml. Suction curettage under was performed due to the diagnosis of molar pregnancy. However, histology of the material was reported as Breus’ mole. There was no evidence for complete?or partial hydatidiform mole. In the genetic examination of the material, no chromosomal abnormality?was detected. Homozygous mutation on factor V leiden gene was determined in the patient.?Breus’ mole should be considered in differential diagnosis of early gestational disorders, and the patients with Breus’mole should be tested for hereditary thrombophilia.
机译:布鲁斯痣是一种罕见的事件,最常见于死胎的胎盘中。它可能发生在有血液循环障碍,复杂性心脏病,高血压,糖尿病和抗凝治疗的患者中。一名没有妊娠的17岁妇女在闭经2个月后因间断性阴道出血和下腹痛入院。入院时,她的一般状况是否正常,生化特征均在正常范围内。超声检查显示子宫增大,囊泡高/低回声。血清β-人绒毛膜促性腺激素(HCG)?为33096 U / ml。由于磨牙妊娠的诊断,进行了刮宫手术。然而,据报道该物质的组织学是勃氏痣。没有证据表明葡萄胎完全或部分葡萄胎。在材料的基因检查中,未检测到染色体异常。在患者中确定了V因子leiden基因的纯合突变。在早期妊娠疾病的鉴别诊断中应考虑勃氏痣,对勃氏痣的患者应进行遗传性血栓形成性检查。

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