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Flucke, U., Vogels, R.J., de Saint Aubain Somerhausen, N., Creytens, D.H., Riedl, R.G., van Gorp, J.M., et al. (2014) Epithelioid Hemangioendothelioma: Clinicopathologic, Immunhistochemical, and Molecular Genetic Analysis of 39 Cases. Diagnostic Pathology, 9, Article No. 131.
https://doi.org/10.1186/1746-1596-9-131

has been cited by the following article:

• TITLE: CT and MRI Findings of Epithelioid Hemangioma of Bone: A Case Report

  AUTHORS: Miaoyin Chen, Liangping Luo

  KEYWORDS: Epithelioid Hemangioma, Bone Tumor, Misdiagnosis, Imaging Diagnosis and Differential Diagnosis

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.14 No.3, March 9, 2026

  ABSTRACT: Epithelioid hemangioma (EH) of bone is a rare, locally aggressive vascular tumor, classified as an intermediate-grade neoplasm in the WHO classification. This article reports a case of a 15-year-old male patient presenting with left knee pain for over one month. Imaging revealed a well-defined osteolytic lesion in the left tibial metaphysis without a sclerotic border or periosteal reaction. MRI showed the lesion to be markedly hyperintense on T2WI, with progressive heterogeneous enhancement post-contrast. Histopathological examination confirmed epithelioid endothelial cell proliferation, supported by a characteristic immunohistochemical profile (CD31+, ERG+), leading to a diagnosis of EH. This case highlights the atypical presentation of EH in an adolescent and emphasizes the role of multimodal imaging and histopathological correlation in diagnosis.