Objective: Capillary hemangiomas are benign vascular lesions involving the skin and soft tissues that commonly occur at birth or an early age. Intracranial capillary hemangiomas are extremely rare; only 14 cases have been reported the literature. Case Description: We describe four patients with capillary hemangiomas. In two of these patients the lesions arose from the cavernous sinus. In the third patient, a large capillary hemangioma arising from the middle cranial fossa extended into the infratemporal fossa. The fourth patient had a left hemorrhagic temporoparietal capillary hemangioma. Results: The first two patients underwent a partial resection, followed by radiotherapy. Local tumor control was achieved in both cases, as shown by the follow-up magnetic resonance imaging. In the third patient the lesion was subtotally removed after embolization. Radiotherapy, performed one year after surgery because of recurrence, allowed tumor control. In the fourth patient surgical removal was total and no adjuvant radiotherapy was required after surgery; follow-up magnetic resonance imaging did not show any recurrence at the one-year follow-up. Conclusion: Surgery is an option for symptomatic intracranial capillary hemangiomas. However, because partial removal is associated with a high recurrence rate, capillary hemangiomas that cannot be removed radically should be treated with radiotherapy, which offers the possibility of controlling lesion size and preventing tumor recurrence. © 2012 Elsevier Inc.

Intracranial capillary hemangioma: A description of four cases / Morace, Roberta; Marongiu, Alessandra; Tommaso, Vangelista; Vittorio, Galasso; Colonnese, Claudio; Giangaspero, Felice; Gualtiero, Innocenzi; Esposito, Vincenzo; Cantore, Giampaolo. - In: WORLD NEUROSURGERY. - ISSN 1878-8750. - STAMPA. - 78:1-2(2012), pp. 15-21. [10.1016/j.wneu.2011.09.017]

Intracranial capillary hemangioma: A description of four cases

MORACE, ROBERTA;MARONGIU, ALESSANDRA;COLONNESE, Claudio;GIANGASPERO, FELICE;ESPOSITO, Vincenzo;CANTORE, Giampaolo
2012

Abstract

Objective: Capillary hemangiomas are benign vascular lesions involving the skin and soft tissues that commonly occur at birth or an early age. Intracranial capillary hemangiomas are extremely rare; only 14 cases have been reported the literature. Case Description: We describe four patients with capillary hemangiomas. In two of these patients the lesions arose from the cavernous sinus. In the third patient, a large capillary hemangioma arising from the middle cranial fossa extended into the infratemporal fossa. The fourth patient had a left hemorrhagic temporoparietal capillary hemangioma. Results: The first two patients underwent a partial resection, followed by radiotherapy. Local tumor control was achieved in both cases, as shown by the follow-up magnetic resonance imaging. In the third patient the lesion was subtotally removed after embolization. Radiotherapy, performed one year after surgery because of recurrence, allowed tumor control. In the fourth patient surgical removal was total and no adjuvant radiotherapy was required after surgery; follow-up magnetic resonance imaging did not show any recurrence at the one-year follow-up. Conclusion: Surgery is an option for symptomatic intracranial capillary hemangiomas. However, because partial removal is associated with a high recurrence rate, capillary hemangiomas that cannot be removed radically should be treated with radiotherapy, which offers the possibility of controlling lesion size and preventing tumor recurrence. © 2012 Elsevier Inc.
2012
capillary hemangioma; middle cranial fossa; cavernous sinus; radiotherapy; surgery
01 Pubblicazione su rivista::01a Articolo in rivista
Intracranial capillary hemangioma: A description of four cases / Morace, Roberta; Marongiu, Alessandra; Tommaso, Vangelista; Vittorio, Galasso; Colonnese, Claudio; Giangaspero, Felice; Gualtiero, Innocenzi; Esposito, Vincenzo; Cantore, Giampaolo. - In: WORLD NEUROSURGERY. - ISSN 1878-8750. - STAMPA. - 78:1-2(2012), pp. 15-21. [10.1016/j.wneu.2011.09.017]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/431577
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