Severe multiple organ failure as a consequence of diabetic ketoacidosis in an adolescent with new-onset type 1 diabetes: A case report

被引:2
|
作者
Modarelli, Rachel [1 ,4 ]
Brown, Lauren [2 ]
Boyd, Jenny [2 ]
Podd, Bradley [2 ]
Willis, Zachary [3 ]
Levenson, Amy [1 ]
机构
[1] Univ N Carolina, Sch Med, Div Pediat Endocrinol, Chapel Hill, NC USA
[2] Univ N Carolina, Sch Med, Div Pediat Crit Care Med, Chapel Hill, NC USA
[3] Univ N Carolina, Sch Med, Div Pediat Infect Dis, Chapel Hill, NC USA
[4] Univ N Carolina, Sch Med, Div Pediat Endocrinol, 127 Med Wing E,CB7039, Chapel Hill, NC 27599 USA
来源
关键词
Pediatric; diabetic ketoacidosis; multiple organ failure; CHILDREN; PREVALENCE; MUCORMYCOSIS; TRENDS;
D O I
10.1177/2050313X231190004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The initial presentation of pediatric diabetes is variable, making prompt diagnosis and treatment challenging. The overlap between type 1 and type 2 diabetes and presence of developmental delays can complicate diagnosis, resulting in delays and severe illness at presentation. Here we describe a case of a 13-year-old male with autism and attention deficit hyperactivity disorder who presented with severe diabetic ketoacidosis, multiple organ failure, and shock. Within 2 weeks of this initial presentation, he had further clinical decompensation due to an intestinal perforation. Cultures from resected gastrointestinal tissue grew mucormycosis, protracting his hospital stay and recovery. He was able to go home several months later with remarkable improvement. This case highlights the necessity of careful history taking and early testing, and how investigation for rare complications of diabetes is vital when patients do not improve as expected.
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页数:4
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