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Complete hydatidiform mole with a surviving coexistent twin in a woman with sickle cell disease: a case report.

机译:患有镰状细胞病的女性中完整的葡萄胎与存活的双胞胎并存:一例病例报告。

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BACKGROUND: Twin pregnancy with an apparently healthy fetus and complete hydatidiform mole (CHMTF) is a rare condition. We present the first reported case in a woman with sickle cell disease. CASE: An 18-year-old woman, para 1, gravida 0, with sickle cell disease was diagnosed at 19 weeks as having a complete molar pregnancy with a coexistent live fetus. The patient presented with abdominal pain, nausea, headaches, body aches, joint pain and chest pain on 2 different occasions. She denied having vaginal bleeding. Whether the patient was having a sickle cell crisis or molar pregnancy symptoms (i.e., thyrotoxicosis) was not clear. She was given intravenous hydration and pain management. All her symptoms resolved, confirming sickle cell crisis as the final diagnosis. The pregnancy was uneventful until 35 weeks, when oligohydramnios prompted induction of labor. Suction curettage was performed after delivery for removal of the molar pregnancy. The patient did not show any evidence of persistent trophoblastic disease 2 months after delivery. CONCLUSION: CHMTF in sickle cell disease patients is challenging. Adequate intravenous hydration and pain management should be started when one suspects a crisis. If the symptoms resolved, thyrotoxicosis due to the molar pregnancy is unlikely. In addition to proper medical management, proper counseling of the patient and close monitoring of both fetus and mother should be undertaken.
机译:背景:双胎妊娠伴明显健康的胎儿和完全的葡萄胎(CHMTF)是一种罕见的疾病。我们介绍了镰状细胞病女性的首例报道病例。病例:一名18岁妇女,第1胎,妊娠0期,患有镰状细胞病,在19周时被诊断为完全磨牙妊娠并存有活胎儿。该患者在2种不同情况下均出现腹痛,恶心,头痛,身体疼痛,关节痛和胸痛。她否认阴道流血。该患者是否患有镰状细胞危机或磨牙妊娠症状(即甲状腺毒症)尚不清楚。她接受了静脉补液和疼痛处理。她的所有症状均得到缓解,确认镰状细胞危机为最终诊断。直到35周,羊水过少提示引产,怀孕才算顺利。分娩后进行刮除术以去除磨牙妊娠。分娩后2个月,患者未显示持续性滋养细胞疾病的任何证据。结论:镰状细胞病患者的CHMTF具有挑战性。当怀疑有危机时,应开始适当的静脉补水和止痛。如果症状消失,则由于磨牙妊娠而引起的甲状腺毒症不太可能发生。除了适当的医疗管理外,还应对患者进行适当的咨询并密切监视胎儿和母亲。

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