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抗酮症糖尿病:一个出现在罕见地区的罕见病例。

Ketosis-resistant diabetes: a rare case in unlikely territory.

作者信息

Wachira John Kelly, Bhatia Vishal

机构信息

Department of Internal Medicine, Sanford School of Medicine, University of South Dakota, USA.

出版信息

S D Med. 2013 Mar;66(3):95, 97-9.

Abstract

BACKGROUND

Ketosis-resistant diabetes is a syndrome that has undergone numerous classification schemes in the past. In 1979, the National Diabetes Data Group (NDDG) introduced an association of malnutrition and diabetes. In 1985, the World Health Organization (WHO) created a new diabetes category called malnutrition-related diabetes mellitus (MRDM). MRDM consisted of two subclasses: fibrocalculous pancreatic diabetes (FCPD) and protein-deficient pancreatic diabetes (PDPD). Ketosis-resistant diabetes of the young (KRDY) was included in the subclass of PDPD. We report a rare case of a 37-year-old Sudanese immigrant with ketosis-resistant diabetes.

CASE

A previously healthy 37-year-old male presented with increased lethargy, polydipsia, polyuria and weight loss for the last seven to eight months. The patient had immigrated to the U.S. from his native country of Sudan about seven years earlier. He was hemodynamically stable. Physical exam was unremarkable with no evidence of retinopathy or neuropathy. Initial laboratory findings revealed a random blood sugar of 1,409 mg/dl and hemoglobin A1C of 17.8 percent. Urinalysis showed negative proteinuria, positive glycosuria, but only trace ketones were detected. Interestingly, the patient's serum ketones were negative. Arterial blood gas revealed PH 7.37, PCO2 47, P02 108 and HCO3 27. Further diagnostic workup revealed C-peptide 0.36, insulin antibodies less than 2, glutamic acid decarboxylase (GAD) antibodies less than 0.5, ICA 512 antibodies 2.9 and negative anti-islet cell antibodies. An abdominal ultrasound did not show any evidence of pancreatic calcifications or any pathology. Aggressive fluid resuscitation and intravenous insulin was initiated. The patient's hospital course was uncomplicated. He responded well to intravenous insulin drip and hydration. He was eventually transitioned to subcutaneous insulin. He was discharged three days later on a home regimen that included Lantus 28 units SQ at night, Novolog 8 units SQ with meals and a sliding scale with Novolog as needed. The patient's recent follow-up appointment revealed adequate glycemic control with HbA1C level of 7 percent.

CONCLUSION

Our patient did not meet criteria for either type 1 or type 2 diabetes mellitus. After a literature review of atypical etiologies of diabetes and comparing them to our patient, we concluded that the most likely diagnosis was KRDY. In light of a high influx of refugees and immigrants to the U.S., we should entertain. KRDY and other rare causes of diabetes mellitus in patients not satisfying criteria of either type 1 or type 2 diabetes.

摘要

背景

抗酮症糖尿病是一种过去经历过众多分类方案的综合征。1979年,美国国家糖尿病数据组(NDDG)提出了营养不良与糖尿病的关联。1985年,世界卫生组织(WHO)创建了一个新的糖尿病类别,称为营养不良相关性糖尿病(MRDM)。MRDM包括两个亚类:纤维钙化性胰腺糖尿病(FCPD)和蛋白质缺乏性胰腺糖尿病(PDPD)。青年抗酮症糖尿病(KRDY)被纳入PDPD亚类。我们报告一例罕见的37岁苏丹移民抗酮症糖尿病病例。

病例

一名此前健康的37岁男性,在过去七到八个月出现嗜睡、多饮、多尿及体重减轻。该患者约七年前从其祖国苏丹移民至美国。他血流动力学稳定。体格检查无异常,未发现视网膜病变或神经病变迹象。初始实验室检查结果显示随机血糖为1409mg/dl,糖化血红蛋白A1C为17.8%。尿液分析显示蛋白尿阴性、糖尿阳性,但仅检测到微量酮体。有趣的是,患者血清酮体为阴性。动脉血气分析显示pH 7.37、PCO2 47、PO2 108及HCO3 27。进一步的诊断检查显示C肽0.36、胰岛素抗体小于2、谷氨酸脱羧酶(GAD)抗体小于0.5、ICA 512抗体2.9及抗胰岛细胞抗体阴性。腹部超声未显示胰腺钙化或任何病变迹象。开始积极的液体复苏和静脉注射胰岛素治疗。患者的住院过程无并发症。他对静脉胰岛素滴注和补液反应良好。最终转为皮下注射胰岛素。三天后出院,居家治疗方案包括每晚皮下注射甘精胰岛素28单位、随餐皮下注射门冬胰岛素8单位以及根据需要使用门冬胰岛素的血糖滑动调整剂量。患者最近的随访预约显示血糖控制良好,糖化血红蛋白A1C水平为7%。

结论

我们的患者不符合1型或2型糖尿病的标准。在对糖尿病的非典型病因进行文献综述并与我们的患者进行比较后,我们得出最可能的诊断是KRDY。鉴于大量难民和移民涌入美国,我们应考虑KRDY及其他不符合1型或2型糖尿病标准患者中糖尿病的罕见病因。

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