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Intramedullary capillary hemangioma associated with hydrocephalus in an infant
Aldo Iannelli1, Giancarlo Lupi, Maura Castagna
1Department of Neurosurgery, University of Pisa, Italy. a.iannelli@ao-pisa.toscana.it
Insights
A rare capillary hemangioma in a 3-month-old infant caused communicating hydrocephalus. Prompt diagnosis and surgical removal of the spinal tumor resolved the condition, highlighting the importance of considering spinal lesions in infant hydrocephalus.
Area of Science:
- Pediatric Neurology
- Neurosurgery
- Vascular Malformations
Background:
- Communicating hydrocephalus in infants can stem from various causes.
- Enlarging head circumference necessitates thorough neuroimaging to identify the underlying pathology.
- Posterior fossa abnormalities are common in pediatric hydrocephalus.
Observation:
- A 3-month-old infant presented with an enlarging head circumference and communicating hydrocephalus.
- Neuroimaging revealed a vascular lesion in the dorsal spinal cord as the likely cause.
- The lesion was identified as a capillary hemangioma upon histological examination.
Findings:
- Successful surgical intervention included cerebrospinal fluid shunt insertion and complete tumor resection.
- The patient's hydrocephalus resolved post-operatively.
- This case represents a previously unreported association between spinal capillary hemangioma and hydrocephalus in this age group.
Implications:
- Spinal lesions should be considered in the differential diagnosis of infant hydrocephalus, especially when the origin is unclear.
- Early detection and treatment of spinal vascular malformations are crucial for managing associated neurological conditions.
- This case expands the understanding of rare causes of pediatric hydrocephalus and informs diagnostic strategies.
Abstract:
This 3-month-old child presented with an enlarging head circumference arising from communicating hydrocephalus with large subarachnoid spaces in the posterior fossa. Neuroimaging performed to clarify the origin and pathogenesis of the hydrocephalus revealed a vascular lesion within the dorsal spinal cord. Insertion of a cerebrospinal fluid shunt and total removal of the spinal tumor were performed successfully. Histological examination of the medullar lesion demonstrated a capillary hemangioma. Proposed mechanisms for increased intracranial pressure and spinal cord lesions are presented. A spinal hemangioma in this age range associated with hydrocephalus has not been reported previously, but spinal lesions must be considered in the presence of hydrocephalus with no clear origin.
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