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Spinal Subarachnoid Hematoma After Cardiac Angiography in an Infant: A Case Report
Tsuyoshi Aihara1, Itaru Hayakawa1, Kenichi Usami2
1Neurology, National Center for Child Health and Development, Tokyo, JPN.
Insights
Spinal subarachnoid hematoma is rare in infants but can cause paralysis. Early diagnosis and intervention are crucial for better outcomes, especially when neurogenic bladder is an early sign.
Area of Science:
- Pediatric Neurology
- Neurosurgery
Background:
- Spinal subarachnoid hematoma (SSA) can lead to severe neurological deficits, including paralysis and vesicorectal dysfunction.
- While rare in infants, prompt diagnosis and surgical intervention for SSA are vital for improving neurological prognosis.
Observation:
- A 22-month-old boy developed fever, oliguria, and lower limb paralysis after cardiac angiography.
- Diagnosis of SSA and spinal cord shock was delayed due to the patient's inability to articulate symptoms.
- The patient experienced persistent bladder and rectal disturbances and lower limb paralysis despite surgical decompression and hematoma removal.
Findings:
- Neurogenic bladder dysfunction can be an early indicator of spinal cord involvement in infants.
- The exact risk factors for SSA in infants remain largely unknown.
- Cardiac angiography may be a potential trigger for SSA, though evidence is limited.
Implications:
- Clinicians should consider spinal cord pathology in infants presenting with bladder compromise.
- Further research is needed to elucidate risk factors for SSA in the pediatric population.
- Early recognition and management of SSA in infants are critical to mitigate long-term neurological sequelae.
Abstract:
Spinal subarachnoid hematoma may result in sequelae such as bilateral lower extremity paralysis and vesicorectal disturbances. Although spinal subarachnoid hematoma is rare in infants, early intervention has been suggested to improve neurological prognosis. Therefore, clinicians are encouraged to make early diagnosis and surgical intervention. A 22-month-old boy was prescribed aspirin for a congenital heart disease. A routine cardiac angiography was performed under general anesthesia. Fever and oliguria developed on the next day, followed by flaccid paralysis of the lower limbs four days later. Five days later, he was diagnosed with spinal subarachnoid hematoma and associated spinal cord shock. Even after emergent posterior spinal decompression, hematoma removal, and rehabilitation, the patient remained with bladder rectal disturbance and flaccid paralysis of both lower limbs. Diagnosis and treatment of this case were delayed mainly because of his difficulty to complain of back pain and paralysis. The neurogenic bladder was one of the first neurological symptoms in our case, so it may be important to consider spinal cord involvement in infants with bladder compromise. Risk factors for spinal subarachnoid hematoma in infants are largely unknown. The patient had undergone a cardiac angiography the day before the onset of the symptoms, which may be related to subarachnoid hematoma. However, similar reports are scarce, with only one case of spinal subarachnoid hematoma reported in an adult following cardiac catheter ablation. Accumulation of evidence regarding risk factors for subarachnoid hematoma in infants is warranted.
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