Cranial and Spinal Epithelioid Hemangioma: Systematic Review and Illustrative Calvarial Case.

Anticancer ResOct 28, 2026

Gianluca Scalia, Gianluca Ferini, Gianluca Galvano et al.

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Condensed from the publisher's abstract. An xxcode editorial summary of this publication has not been generated yet.

From the abstract

Cranial and neuraxial epithelioid hemangioma (EH) is exceptionally rare and anatomically heterogeneous. We systematically reviewed reported cerebral, cranial osseous, primary non-osseous spinal epidural, and vertebral-origin EH with clinically relevant neuraxial extension and present an illustrative hypervascular calvarial case.

Reported results

Twenty-two reports were included: 14 (63.6%) vertebral-origin and eight (36.4%) cerebral, combined calvarial-cerebral, cranial osseous, or primary non-osseous spinal epidural. Surgery was reported in 19/22 publications (86.4%), radiotherapy in 10/22 (45.5%), and preoperative embolization in 3/22 (13.6%).

Authors' conclusions

Cranial and neuraxial EH is rare, with published evidence dominated by vertebral disease. Management should be individualized according to anatomical compartment, neural compression, structural instability, and vascularity. Histological distinction from epithelioid hemangioendothelioma and angiosarcoma is essential, while the available evidence is insufficient to establish comparative efficacy of radiotherapy or…

Source

Published in Anticancer Res. The text above is extracted from the publisher's own abstract and has not been edited by xxcode. For clinical decisions, review the original publication.

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