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Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
Published on: October 20, 2017
A case of cerebellar capillary hemangioma with multiple cysts
Atsushi Uyama1, Atsuhumi Kawamura, Hideyuki Akiyama
1Department of Neurosurgery, Hyogo Prefectural Kobe Children's Hospital, Kobe, Japan. auyama811@yahoo.co.jp
Insights
Intracranial capillary hemangiomas are rare brain tumors. This case highlights successful surgical and neuroendoscopic treatment for a pediatric patient with a complex intracranial capillary hemangioma and hydrocephalus.
Area of Science:
- Pediatric Neurosurgery
- Vascular Neurology
Background:
- Intracranial capillary hemangiomas are exceptionally rare vascular malformations.
- Recent reports indicate an increase in spinal capillary hemangioma diagnoses.
- This study focuses on a unique pediatric case with intracranial involvement.
Observation:
- A 4-month-old female presented with hydrocephalus and a cerebellar mass.
- The patient exhibited widespread cutaneous and visceral hemangiomas.
- Brain imaging revealed a cystic cerebellar lesion causing obstructive hydrocephalus.
Findings:
- Histopathological examination confirmed capillary hemangioma.
- Neuroendoscopic fenestration and surgical resection were performed.
- The patient experienced no postoperative recurrence.
Implications:
- This case demonstrates the efficacy of combined surgical and neuroendoscopic approaches.
- Early diagnosis and intervention are crucial for managing intracranial capillary hemangiomas.
- Surgical management should be considered for intracranial capillary hemangiomas.
Abstract:
Intracranial capillary hemangiomas are very rare, though several spinal capillary hemangiomas have recently been reported. We report here a case of intracranial capillary hemangioma with multiple cysts and review the current literature of similar cases. A 4-month-old girl was referred to our hospital for treatment of hydrocephalus and a cerebellar mass lesion. She presented with hemangiomas distributed widely over the body, as well as disseminated hemangiomas in the pleura, liver, spleen, pancreas, kidneys and vagina. Pathological examination of the specimen from the vagina confirmed the diagnosis of a capillary hemangioma made at another hospital. Radiological examination of the brain revealed a cystic mass lesion in the left cerebellar hemisphere with subsequent obstructive hydrocephalus. The cysts extended upward into the bilateral ventricle. Following neuroendoscopic fenestration of the cysts, resection of the left cerebellar mass was performed. Histological examination of the lesion demonstrated similarly sized capillaries, and the pathological diagnosis was confirmed as capillary hemangioma. There was no recurrence postoperatively. Our patient was treated successfully by surgical resection and neuroendoscopic procedures. Surgical intervention may therefore be indicated in intracranial capillary hemangiomas.
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