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Updated: Oct 8, 2026

A Thrombotic Stroke Model Based On Transient Cerebral Hypoxia-ischemia
Published on: August 18, 2015
Thrombotic stroke in a child with diarrhea-associated hemolytic-uremic syndrome with a good recovery
T Nakahata1, H Tanaka, T Tateyama
1Department of Pediatrics, Hirosaki University School of Medicine, Japan.
Insights
A child with post-diarrheal hemolytic-uremic syndrome (HUS) experienced seizures and stupor but recovered fully. This case suggests that neurological complications in HUS may not always lead to severe long-term morbidity.
Area of Science:
- Pediatric Nephrology
- Neurology
- Infectious Diseases
Background:
- Hemolytic-uremic syndrome (HUS) is a serious condition often triggered by infections like E. coli.
- Neurological complications, including seizures and altered consciousness, can occur in HUS.
- Early diagnosis and intervention are crucial for managing HUS and its sequelae.
Observation:
- A 3.5-year-old boy presented with post-diarrheal HUS, characterized by bloody diarrhea, abdominal pain, fever, seizures, and anuria.
- Laboratory findings revealed elevated blood urea nitrogen and creatinine, with significantly decreased platelet count.
- Cranial CT scan showed infarction and edema in the basal ganglia, indicating significant neurological involvement.
Findings:
- The patient required continuous hemodiafiltration for anuria and persistent stupor.
- Despite severe neurological lesions and prolonged anuria, the patient demonstrated a remarkable recovery without lasting complications.
- Positive IgM antibody titers to Escherichia coli O157 confirmed the infectious etiology.
Implications:
- This case highlights the potential for neurological recovery in children with HUS, even with extensive brain lesions.
- It suggests that aggressive supportive care, including renal replacement therapy, can improve outcomes in severe HUS cases.
- Further research is warranted to understand the factors influencing neurological recovery and long-term morbidity in HUS patients.
Abstract:
A boy aged 3.5 years with post-diarrheal hemolytic-uremic syndrome (HUS) was referred to our hospital because of convulsion and stupor. He had been admitted to a regional hospital with a 3-day history of bloody diarrhea, colic abdominal pain and fever. Two days later, he had complained of generalized seizures and oliguria. On admission, he developed anuria, and serum blood nitrogen and creatinine increased to 56 mg/100 ml and 2.8 mg/100 ml, respectively. Platelets decreased to 42,000/microl. Under the diagnosis of HUS, a continuous hemodiafiltration treatment had to be instituted. Computed tomography of his head at hospital day 5 revealed abnormal low density area of infarction with edema in both the basal ganglia involving with the posterior limb of internal capsule. Serum titer of IgM antibody to Escherichia coli O157 showed positive value. Although his anuria and stupor persisted over 10 days, he recovered without serious complications. These clinical observations may indicate that patients with similar lesions do not necessarily have serious morbidity.
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