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DOI 10.3171/jns.2004.101.1.0073

Медицинская библиотека · Journal of neurosurgery · 2004

Capillary hemangioma of the central nervous system.

Abe Masamitsu, Tabuchi Kazuo, Tanaka Shin, Hodozuka Akira, Kunishio Katsuzo, Kubo Naohiko, Nishimura Yukimasa

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Аннотация

OBJECT: Capillary hemangiomas are benign tumors or tumorlike lesions that originate from blood vessels and have rarely been reported to develop in the brain or spinal cord. The authors summarize the clinical and histological features of capillary hemangiomas of the central nervous system (CNS).

METHODS

The clinical features, imaging characteristics, and outcomes in 10 patients with CNS capillary hemangiomas were reviewed. Histological studies included immunostaining with CD31, alpha-smooth muscle actin, vascular endothelial growth factor, and Ki-67 antigen. Three patients with lesions in the brain presented with symptoms of increased intracranial pressure or seizures. Seven patients with lesions in the spinal cord presented with progressive sensorimotor disturbances of the lower limbs. Computerized tomography and magnetic resonance imaging demonstrated well-defined, enhancing lesions associated with marked perifocal edema. Angiography demonstrated hypervascular lesions, which have not recurred after resection. In two cases, multiple satellite lesions resolved after the systemic administration of steroid drugs or interferon-alpha. Histologically, all lesions were consistent with findings of capillary hemangioma of the skin or soft tissues. The CNS lesions differed significantly from other vascular neoplasms, such as hemangioendotheliomas, hemangiopericytomas, and hemangioblastomas.

CONCLUSIONS

Capillary hemangiomas of the CNS are benign lesions that can be surgically removed and cured without adjuvant therapy.

Для цитирования: Abe Masamitsu, Tabuchi Kazuo, Tanaka Shin, Hodozuka Akira, Kunishio Katsuzo, Kubo Naohiko, Nishimura Yukimasa. Capillary hemangioma of the central nervous system.. Journal of neurosurgery. 2004. DOI: 10.3171/jns.2004.101.1.0073.

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