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Type 1 Diabetes Associated with Asymptomatic Acromegaly Successfully Treated with Surgery after Pregnancy: A Case Report

机译:合并无症状性肢端肥大症的1型糖尿病经手术成功治疗:1例报道

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References(22) Cited-By(1) We report a rare case of type 1 diabetes in a woman associated with acromegaly who was treated with surgery after pregnancy. An 18-year-old woman came to our hospital in April, 1998, complaining of thirst, polydipsia, polyuria, appetite loss, body weight loss of 8 kg in a month, and amenorrhea beginning 2 months earlier. Based on laboratory data, she was diagnosed as having type 1 diabetes mellitus. Although we suspected her of having acromegaly because of high growth hormone (GH) levels (6.9 or 8.5 ng/ml), blood levels of insulin-like growth factor 1 (IGF-1) and IGF-binding protein-3 (IGFBP-3) were within normal range and the circadian rhythm of her blood GH levels was normally maintained. Her blood GH level was elevated to 12.6 ng/ml 15 minutes after a TRH administration. Blood GH levels were suppressed from 49 ng/ml to 1.5 ng/ml 4 hours after an oral administration of 2.5 mg of bromocriptine. A magnetic resonance images (MRIs) showed pituitary swelling, but no nodules were found in the pituitary. Therefore, we diagnosed her as having acromegaly and observed her without surgery, while prescribing diet therapy and intensive insulin therapy for diabetes. We started a treatment of oral administration of 7.5 mg of bromocriptine per day for the acromegaly from April 28, 2000, because her elevated GH was suspected of causing her diabetes to be poorly controlled. During a pregnancy from October, 2000 to September, 2001, diabetic control was improved with increased administration of insulin under a constant dose of bromocriptine. She delivered a normal full-term infant. After the bromocriptine therapy was stopped as she hoped to breastfeed, blood levels of GH and IGF-1 became elevated and her diabetic control deteriorated. As her pituitary tumor observed in pituitary MRIs became larger during the course, a transsphenoidal surgery was performed on March 8, 2002. After the surgery, blood levels of GH and IGF-1 lowered and diabetic control improved again. We concluded as follows: to rule out acromegaly in patients with poorly controlled diabetes, 1) measurements of serum GH and IGF-1 should be performed, and 2) pituitary MRIs should be performed if blood levels of GH or IGF-1 are high.
机译:参考文献(22)被引(1)我们报道了一名患有肢端肥大症的妇女在妊娠后接受手术治疗的罕见1型糖尿病病例。 1998年4月,一名18岁妇女因口渴,烦渴,多尿,食欲不振,每月体重减轻8公斤以及2个月前开始闭经而来我们医院就诊。根据实验室数据,她被诊断患有1型糖尿病。尽管我们怀疑她由于高生长激素(GH)水平(6.9或8.5 ng / ml)而患有肢端肥大症,但血液中的胰岛素样生长因子1(IGF-1)和IGF结合蛋白3(IGFBP-3 )处于正常范围内,她的血液GH水平的昼夜节律正常维持。给予TRH后15分钟,她的血液GH水平升高至12.6 ng / ml。口服2.5 mg溴隐亭4小时后,血液GH水平从49 ng / ml降至1.5 ng / ml。磁共振图像(MRI)显示垂体肿胀,但在垂体中未发现结节。因此,我们诊断出她患有肢端肥大症,并观察她未经手术,同时规定了糖尿病的饮食疗法和强化胰岛素疗法。我们从2000年4月28日开始对肢端肥大症每天口服7.5毫克溴隐亭的口服治疗,因为怀疑她的GH升高导致糖尿病控制不佳。在2000年10月至2001年9月的怀孕期间,通过在恒定剂量的溴隐亭下增加胰岛素的施用,可以改善糖尿病的控制。她分娩了一个正常的足月婴儿。在她希望母乳喂养的溴隐亭治疗停止后,GH和IGF-1的血药浓度升高,糖尿病控制恶化。由于在垂体MRI中观察到的垂体瘤变大,于2002年3月8日进行了经蝶窦手术。手术后,GH和IGF-1的血药水平降低,糖尿病控制再次改善。我们得出以下结论:为了排除控制不良的糖尿病患者的肢端肥大症,应进行以下检查:1)血液中GH和IGF-1的测量,以及2)如果GH或IGF-1的血液水平高,则应进行垂体MRI。

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