Diabetic ketoacidosis and cerebral edema: a rare case of infarct-like MRI findings in a pediatric patient.

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2025-05-12 eCollection Date: 2025-06-01 DOI:10.1097/MS9.0000000000003332
Maryam Kachuei, Shayan Eghdami, Ramin Zareh, Samaneh Azimi-Souteh
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Abstract

Introduction and importance: Diabetic ketoacidosis (DKA) is a serious and potentially life-threatening complication of type 1 diabetes mellitus, particularly in pediatric patients. Cerebral edema (CE) is a rare but devastating consequence of DKA. Although neuroimaging findings in CE are typically nonspecific, infarct-like changes are exceedingly rare and may complicate clinical management.

Case presentation: We report the case of an 11-year-old boy with a history of type 1 diabetes mellitus who presented with epigastric pain, vomiting, polydipsia, and polyuria. Despite timely initiation of standard treatment for DKA, the patient developed acute neurological deterioration consistent with CE. Brain MRI revealed restricted diffusion in the basal ganglia, corpus callosum, and internal capsule - findings suggestive of infarction rather than typical vasogenic edema.

Clinical discussion: This case highlights the diagnostic and therapeutic challenges posed by DKA-associated CE with atypical imaging findings. The observed infarct-like MRI pattern is rarely reported and may reflect underlying cytotoxic edema or ischemic injury. Understanding the multifactorial pathophysiology - including osmotic shifts, inflammatory processes, and impaired cerebral autoregulation - is critical for effective management.

Conclusion: Early recognition of atypical cerebral involvement in pediatric DKA is essential. Advanced neuroimaging can aid in diagnosis and guide appropriate intervention. Clinicians should remain vigilant for neurological complications even during early phases of treatment and consider infarct-like patterns in differential diagnosis.

糖尿病酮症酸中毒和脑水肿:一个罕见的病例梗死样MRI发现的儿童患者。
简介及重要性:糖尿病酮症酸中毒(DKA)是1型糖尿病的一种严重且可能危及生命的并发症,尤其是在儿科患者中。脑水肿(CE)是DKA的一种罕见但毁灭性的后果。虽然CE的神经影像学表现通常是非特异性的,但梗死样改变极为罕见,可能使临床治疗复杂化。病例介绍:我们报告一个11岁的男孩,有1型糖尿病病史,表现为胃脘痛、呕吐、烦渴和多尿。尽管及时开始了DKA的标准治疗,但患者出现了与CE一致的急性神经功能恶化。脑MRI显示基底节区、胼胝体和内囊弥散受限,提示梗死,而不是典型的血管源性水肿。临床讨论:本病例强调了dka相关CE与非典型影像学表现所带来的诊断和治疗挑战。观察到的梗死样MRI模式很少报道,可能反映潜在的细胞毒性水肿或缺血性损伤。了解多因素病理生理学——包括渗透转移、炎症过程和大脑自动调节受损——对有效治疗至关重要。结论:儿童DKA不典型脑受累的早期识别至关重要。先进的神经影像学可以帮助诊断和指导适当的干预。临床医生即使在早期治疗阶段也应对神经系统并发症保持警惕,并在鉴别诊断时考虑梗死样模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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5.90%
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