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[Epithelioid hemangioma: a clinicopathologic analysis of 7 cases]. | LitMetric

AI Article Synopsis

  • The study focuses on the clinicopathologic features and diagnostic aspects of epithelioid hemangioma, analyzing 7 cases from skin, bone, and venous vessels.
  • Patients ranged from 14 to 54 years old, presenting with various symptoms, including erythematous nodules on the skin and osteolytic lesions in bones; the tumors exhibited distinct morphological characteristics.
  • Epithelioid hemangioma is a rare benign tumor with similar presentations to other conditions, but it typically shows no recurrence or metastasis after treatment, making it curable.

Article Abstract

Objective: To study the clinicopathologic features, diagnosis and differential diagnosis of epithelioid hemangioma.

Methods: The morphologic features of 7 cases of epithelioid hemangioma of skin, bone and venous vessels were studied.

Results: There were altogether 4 male and 3 female patients (median age = 34 years; age range from 14 to 54 years). The 3 skin cases presented as single or multiple erythematous to bluish nodules or papules, with or without itchiness. The 2 bone cases appeared as osteolytic expansile lesions on radiologic examination. The remaining 2 cases involved medium-sized venous structures and presented as small isolated nodules in soft tissue. Histologically, the lesions were characterized by the presence of exuberant endothelial proliferations with various degree of inflammatory reaction. The neoplastic endothelial cells were plump, eosinophilic and polygonal, forming vascular channels. Occasional solid sheet-like arrangement was demonstrated. Intracytoplasmic vacuoles were commonly identified, indicating formation of primary lumen. The surrounding stroma contained various number of eosinophils and lymphoplasmacytic cells. Immunohistochemical study showed that the tumor cells were positive for endothelial markers (CD31 and CD34) and negative for epithelial marker (cytokeratin). Follow-up information was available in 6 cases. The duration of follow-up ranged from 5 to 36 months (median = 14 months). There was no evidence of recurrence or distant metastasis.

Conclusions: Epithelioid hemangioma is a rare benign curable lesion which can be multifocal, involving skin, soft tissue and bone. It needs to be distinguished from Kimura's disease and epithelioid hemangioendothelioma.

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