Angiosarcoma is a rare vascular malignant neoplasm that mainly occurs in skin and soft tissues. Intracranial localization is very rare and only a few cases have been reported. This report intends to present the clinical, radiological and pathological pictures of a primary central nervous system angiosarcoma along with a review of the literature. A 35-year-old woman presented at our institution with weakness and sensory disturbances of her right hand. Neuroimaging revealed a roughly round, hemorrhagic and moderately enhancing lesion in the left frontal posterior region. The tumor was totally removed under awake anesthesia and continuous monitoring of motor and language functions. Histopathology revealed an epithelioid angiosarcoma. Radical removal, followed by adjuvant radiotherapy and chemotherapy, is able to completely control the disease for a relatively long period.

Primary central nervous system angiosarcoma : a case report and literature review / E. La Corte, F. Acerbi, M. Schiariti, M. Broggi, E. Maderna, B. Pollo, R. Nunziata, E. Maccagnano, P. Ferroli. - In: NEUROPATHOLOGY. - ISSN 0919-6544. - 35:2(2015 Apr), pp. 184-191.

Primary central nervous system angiosarcoma : a case report and literature review

E. La Corte
;
F. Acerbi;M. Schiariti;M. Broggi;
2015

Abstract

Angiosarcoma is a rare vascular malignant neoplasm that mainly occurs in skin and soft tissues. Intracranial localization is very rare and only a few cases have been reported. This report intends to present the clinical, radiological and pathological pictures of a primary central nervous system angiosarcoma along with a review of the literature. A 35-year-old woman presented at our institution with weakness and sensory disturbances of her right hand. Neuroimaging revealed a roughly round, hemorrhagic and moderately enhancing lesion in the left frontal posterior region. The tumor was totally removed under awake anesthesia and continuous monitoring of motor and language functions. Histopathology revealed an epithelioid angiosarcoma. Radical removal, followed by adjuvant radiotherapy and chemotherapy, is able to completely control the disease for a relatively long period.
Brain angiosarcoma; Central nervous system tumor; Neurosurgery; Survival; Treatment; Adolescent; Adult; Aged; Brain Neoplasms; Child; Child, Preschool; Female; Hemangiosarcoma; Humans; Infant; Infant, Newborn; Male; Middle Aged; Young Adult; 2734; Neurology (clinical); Medicine (all)
Settore MED/27 - Neurochirurgia
Settore MED/08 - Anatomia Patologica
apr-2015
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/466859
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