A new onset drug induced diabetes mellitus presenting with diabetic ketoacidosis in a child undergoing treatment for B cell acute lymphoblastic leukemia. A case report and review of literature.

IF 1.3 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Preeti Sharma, Varuna Vyas, Siyaram Didel, Kuldeep Singh
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Abstract

Objectives: Hyperglycemia is a known side effect of anticancer chemotherapeutic drugs. This entity known as drug-induced diabetes mellitus usually does not present with the development of diabetic ketoacidosis (DKA). We hereby report a case of drug induced diabetes mellitus in a child with acute leukemia presenting with DKA.

Case presentation: We report a case of a teenage boy diagnosed with B cell acute lymphoblastic leukemia and was started on induction phase chemotherapy as per the Indian Collaborative Childhood Leukemia group (ICICLe) acute lymphoblastic leukemia-14 protocol. On day 12 of the induction phase, he developed hyperglycemia and presented to us with severe diabetic ketoacidosis (DKA). Serum anti glutamic acid decarboxylase 65 antibody levels were negative with low serum C peptide levels. Initially, the possibility of drug-induced acute pancreatitis was kept which was ruled out. Keeping the possibility of drug-induced hyperglycemia, the child was started on subcutaneous regular insulin which was titrated as per sugar records. Continuation of remaining chemotherapy was done by PEGylated L-asparaginase with titration of insulin as per home-based sugar records. Insulin requirement increased from 0.3 unit/kg/day to a maximum of 1 unit/kg/day during consolidation phase 1 with PEGylated L-asparaginase suggesting drug-induced hyperglycemia but subsequently insulin requirement decreased and insulin was stopped.

Conclusions: Drug induced diabetes mellitus can present as DKA during induction phase of acute lymphoblastic leukemia (ALL) chemotherapy. A high index of suspicion and close monitoring are required. The insulin requirements in these patients can be very fluctuant and may become nil during the course of treatment.

一名正在接受 B 细胞急性淋巴细胞白血病治疗的儿童新发药物性糖尿病并伴有糖尿病酮症酸中毒。病例报告和文献综述。
目的:众所周知,高血糖是抗癌化疗药物的副作用之一。这种被称为药物诱发糖尿病的实体通常不会出现糖尿病酮症酸中毒(DKA)。我们在此报告一例急性白血病患儿因药物诱发糖尿病而出现 DKA 的病例:我们报告了一例被诊断为 B 细胞急性淋巴细胞白血病的十几岁男孩,他按照印度儿童白血病协作组(ICICLe)急性淋巴细胞白血病-14 方案开始接受诱导期化疗。在诱导阶段的第 12 天,他出现了高血糖,并因严重的糖尿病酮症酸中毒(DKA)而就诊。血清抗谷氨酸脱羧酶 65 抗体水平阴性,血清 C 肽水平较低。初步排除了药物诱发急性胰腺炎的可能性。考虑到药物诱发高血糖的可能性,患儿开始皮下注射常规胰岛素,并根据血糖记录调整剂量。继续使用聚乙二醇化 l-天冬酰胺酶进行剩余化疗,并根据家庭血糖记录滴定胰岛素。在使用聚乙二醇化 l-天冬酰胺酶的巩固治疗第一阶段,胰岛素需求量从 0.3 单位/公斤/天增加到最高 1 单位/公斤/天,这表明药物诱发了高血糖,但随后胰岛素需求量减少,胰岛素也停止使用:结论:在 ALL 化疗的诱导阶段,药物诱发的糖尿病可表现为 DKA。需要高度怀疑并密切监测。这些患者的胰岛素需求量可能波动很大,在治疗过程中可能会变成零。
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来源期刊
CiteScore
2.70
自引率
7.10%
发文量
176
审稿时长
3-6 weeks
期刊介绍: The aim of the Journal of Pediatric Endocrinology and Metabolism (JPEM) is to diffuse speedily new medical information by publishing clinical investigations in pediatric endocrinology and basic research from all over the world. JPEM is the only international journal dedicated exclusively to endocrinology in the neonatal, pediatric and adolescent age groups. JPEM is a high-quality journal dedicated to pediatric endocrinology in its broadest sense, which is needed at this time of rapid expansion of the field of endocrinology. JPEM publishes Reviews, Original Research, Case Reports, Short Communications and Letters to the Editor (including comments on published papers),. JPEM publishes supplements of proceedings and abstracts of pediatric endocrinology and diabetes society meetings.
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