Choy Kay Hau Aaron, Wong Tang, Cao Rena H M, Flack Jeff R
Department of Endocrinology and Diabetes, Barwon Health, Geelong, Victoria, Australia.
Diabetes Centre, Bankstown-Lidcombe Hospital, Bankstown, New South Wales, Australia.
Endocrinol Diabetes Metab Case Rep. 2022 Jul 1;2022. doi: 10.1530/EDM-22-0262.
Fulminant type 1 diabetes mellitus (FT1DM) is characterised by extremely rapid destruction of pancreatic beta cells. An association between FT1DM and pregnancy has been reported and can lead to unfavourable pregnancy outcomes without timely treatment. We report a case of FT1DM in a pregnancy with gestational diabetes mellitus (GDM), the first of its kind in the English literature to date. A 27-year-old woman with insulin-requiring GDM presented with rapidly deteriorating glycaemic control in her third trimester of pregnancy despite good concordance to treatment. The investigation identified the hallmarks of FT1DM: hyperglycaemia with acute metabolic decompensation and non-immune-mediated beta-cell failure. She received prompt treatment with intravenous insulin therapy and was transitioned to subcutaneous insulin once biochemical improvement had been achieved, albeit with higher insulin requirements than before. She had a good pregnancy outcome and delivered a healthy male infant 5 weeks later through induction of labour. Due to persistent beta-cell dysfunction, she remained on basal-bolus insulin postpartum. This case highlights the importance of early recognition and treatment of FT1DM in pregnancy to prevent adverse maternal and fetal prognoses.
Fulminant type 1 diabetes mellitus (FT1DM) is a subtype of type 1 diabetes characterised by extremely rapid beta-cell destruction, leading to abrupt-onset hyperglycaemia with ketosis or ketoacidosis. The pathognomonic characteristics of FT1DM include the development of diabetic ketosis or ketoacidosis typically within 7 days after the onset of symptoms of hyperglycaemia, a near-normal level of glycated haemoglobin despite elevated plasma glucose levels and the absence of islet cell autoantibodies. The pathophysiology of FT1DM is unclear but the association with genetic predisposition, viral infection and pregnancy has been reported. Due to its predilection for pregnancy, clinicians should have a high index of suspicion for FT1DM in pregnant women with rapidly progressing hyperglycaemic ketoacidosis. As diabetic ketoacidosis in pregnancy is associated with adverse maternal and fetal outcomes, immediate initiation of treatment in pregnant women with suspected FT1DM is extremely vital to prevent morbidity and mortality, even if investigations are still underway. Patients with FT1DM require lifelong insulin therapy due to the complete loss of beta-cell function.
暴发性1型糖尿病(FT1DM)的特征是胰腺β细胞极度快速地被破坏。已有报道称FT1DM与妊娠有关,若不及时治疗可导致不良妊娠结局。我们报告了一例合并妊娠期糖尿病(GDM)的妊娠患者发生FT1DM的病例,这是迄今为止英文文献中首例此类病例。一名患有需胰岛素治疗的GDM的27岁女性,尽管治疗依从性良好,但在妊娠晚期血糖控制迅速恶化。检查发现了FT1DM的特征:伴有急性代谢失代偿的高血糖症和非免疫介导的β细胞功能衰竭。她接受了静脉胰岛素治疗的及时治疗,生化指标改善后转为皮下胰岛素治疗,尽管胰岛素需求量比以前更高。她妊娠结局良好,5周后通过引产分娩出一名健康男婴。由于β细胞功能持续存在障碍,产后她仍需使用基础-餐时胰岛素治疗。该病例突出了妊娠期间早期识别和治疗FT1DM对于预防不良母婴预后的重要性。
暴发性1型糖尿病(FT1DM)是1型糖尿病的一种亚型,其特征是β细胞极度快速地被破坏,导致伴有酮症或酮症酸中毒的急性高血糖症。FT1DM的特征性表现包括通常在高血糖症状出现后7天内发生糖尿病酮症或酮症酸中毒、尽管血浆葡萄糖水平升高但糖化血红蛋白水平接近正常以及不存在胰岛细胞自身抗体。FT1DM的病理生理学尚不清楚,但已有报道称其与遗传易感性。由于其对妊娠的偏好,临床医生对于血糖快速进展为酮症酸中毒的孕妇应高度怀疑FT1DM。由于妊娠期间的糖尿病酮症酸中毒与不良母婴结局相关,对于疑似FT1DM的孕妇立即开始治疗对于预防发病和死亡极为关键,即使仍在进行检查。由于β细胞功能完全丧失,FT1DM患者需要终身胰岛素治疗。