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首页> 外文期刊>BMC research notes >Poor pregnancy outcome after octreotide treatment during pregnancy for familial hyperinsulinemic hypoglycemia: a case report
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Poor pregnancy outcome after octreotide treatment during pregnancy for familial hyperinsulinemic hypoglycemia: a case report

机译:糖尿肽在妊娠期间妊娠期妊娠结局差,为家族性高胰岛素血症低血糖症治疗:案例报告

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Background Late familial hyperinsulinemic hypoglycemia is characterized by recurrent episodes of hypoglycemia and an inappropriate insulinemic response. Treatment with octreotide (somatostatin analogue) reduces the prevalence of clinical significant hypoglycemia and might be beneficial during pregnancy. To our knowledge this is the first report of a woman with late familial hyperinsulinemic hypoglycemia experiencing pregnancies with and without octreotide treatment. Case presentation A 35-year-old Caucasian woman known to suffer from late familial hyperinsulinemic hypoglycemia due to a well-known mutation in the insulin receptor gene has been pregnant 6 times. The patient was treated with injections of Sandostatin LAR? (octreotide) during the first four pregnancies. Her first pregnancy in 1999 was unknown until approximately 25th gestational weeks with fatal intrauterine growth retardation. The following two pregnancies were terminated on parental request after a chorion villus biopsy revealed the mutation causing late familial hyperinsulinemic hypoglycemia. During the fourth pregnancy, in which the fetus also had the mutation, serial ultrasound examinations showed a small fetus with appropriate growth. At birth the girl was small for gestational age. She was admitted to the neonatal special care unit due to low blood glucose and intravenous glucose and early feeding was initiated. One day old, her condition deteriorated with signs of an abdominal catastrophe indicating necrotizing enterocolitis. After two laparotomies – both confirming necrotizing enterocolitis - the child died 8?days after birth. In the following two pregnancies Sandostatin LAR? was stopped before pregnancy and the patient was treated only with diet restriction and intensive glucose monitoring. Both pregnancies ended successfully. One child carried the mutation and was small for gestational age at birth while the other child did not carry the mutation and had normal birth weight. Conclusion In a woman with late familial hyperinsulinemic hypoglycemia octreotide was given during the first four pregnancies resulting in 2 cases of early termination of pregnancy on parental request and 2 cases of inappropriate fetal growth and unviable outcome. The following two pregnancies treated with diet only had a successful outcome.
机译:背景后期家族性高胰岛素血症低血糖的特征在于经复制的低血糖发作和不适当的胰岛素反应。用奥西曲霉(生长抑制素类似物)治疗减少了临床显着的低血糖的患病率,并且在怀孕期间可能是有益的。据我们所知,这是一名患有晚期性高胰岛素血症低血糖的第一份报告,经历患有和不含八炔病治疗的怀孕。案例介绍由于胰岛素受体基因的众所周知的突变已怀孕6次,这已知一名已知患有晚期性高胰岛素血症低血糖的35岁的白种人妇女。患者用桑松汀的注射治疗? (Octreotide)在前四次怀孕期间。她在1999年的第一次怀孕未知,直至大约第25个妊娠周,患有致命的宫内生长迟缓。在绒毛膜绒毛活检显示后,终止了以下两次怀孕终止了患有晚期性高胰岛素脑血症低血糖的突变。在第四次妊娠期间,胎儿还具有突变,连续超声检查显示出具有适当生长的小胎儿。出生时,这个女孩们很小的胎龄。由于低血糖和静脉内葡萄糖和早期饲喂,她被录取为新生儿特殊护理单元。有一天,她的病情恶化了腹部灾难的迹象,表明坏死性小肠结肠炎。经过两次剖腹术后 - 既确认坏死性肠关系炎 - 孩子均在出生后8天死亡。在以下两次怀孕中塞司汀大?在怀孕前停止,患者只用饮食限制和密集的葡萄糖监测治疗。这两个妊娠都成功结束。一个孩子携带突变,在出生时患者少,而另一个孩子没有携带突变并具有正常的出生体重。结论在前四次怀孕期间给出了患有晚期性高胰岛素血症低血糖性低血糖症的女性中,导致2例怀孕早期终止孕妇请求和2例不适当的胎儿生长和不可行的结果。随后用饮食治疗的两次怀孕只有成功的结果。

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