Miscarriage in a patient with Glanzmann Thrombasthenia and low ovarian reserve: A case report

I. E. Uluisik, M. Sonkaya, N. Dokuzeylul Gungor
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Abstract

Glanzmann thrombasthenia (GT), which has an autosomal inheritance pattern, is a hemorrhagic disorder mostly complicated by mucocutaneous bleeding. The severity of this bleeding disorder varies from mild bruising to frequent severe bleeding. Prepartum, peripartum and postpartum bleeding risks are increased in these patients. In addition to the hemorrhagic complications that endanger maternal and fetal well-being, the risk of miscarriage is increased due to maternal antibodies to the platelets found on conceptus-derived trophoblast (placental) cells. In this case report, we report a patient who had a miscarriage in 7+1 week. Our patient had GT, low ovarian reserve, HPV positivity, bilateral dermoid cyst and was complicated by infertility.
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格兰兹曼血栓性贫血合并卵巢储备不足患者流产1例
Glanzmann血栓减少症(GT)是一种常染色体遗传型的出血性疾病,多并发皮肤粘膜出血。这种出血性疾病的严重程度从轻微的瘀伤到频繁的严重出血不等。这些患者的产前、围生期和产后出血风险增加。除了危及母体和胎儿健康的出血性并发症外,由于母体在母体滋养细胞(胎盘)细胞中发现的血小板抗体,流产的风险也会增加。在本病例报告中,我们报告了一例在7+1周内流产的患者。我们的患者有GT,卵巢储备不足,HPV阳性,双侧皮样囊肿并合并不孕症。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
32
期刊介绍: The Tokai Journal of Experimental and Clinical Medicine, also referred to as Tokai Journal, is an official quarterly publication of the Tokai Medical Association. Tokai Journal publishes original articles that deal with issues of clinical, experimental, socioeconomic, cultural and/or historical importance to medical science and related fields. Manuscripts may be submitted as full-length Original Articles or Brief Communications. Tokai Journal also publishes reviews and symposium proceedings. Articles accepted for publication in Tokai Journal cannot be reproduced elsewhere without written permission from the Tokai Medical Association. In addition, Tokai Journal will not be held responsible for the opinions of the authors expressed in the published articles.
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