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Abstract:

This transcript describes Angiolymphoid Hyperplasia with Eosinophilia (ALHE), also referred to as Epithelioid Hemangioma. The discussion focuses on its distinctive histopathological characteristics, such as nodular lymphocytic aggregates with germinal centers and vessels lined by unusually plump, epithelioid endothelial cells that nearly obliterate the lumen. Commonly presenting on the temple, often linked to a damaged temporal artery, its classification as a neoplasm versus a reactive lesion remains a subject of debate. A significant clinical consideration highlighted is the differential diagnosis with robust insect bite reactions and Lymphomatoid Papulosis (LYP), particularly given that all three entities can exhibit CD30 positive reactive immunoblasts, underscoring the necessity for comprehensive clinical correlation.

Angiolymphoid Hyperplasia with Eosinophilia (ALHE): Key Characteristics and Differential Diagnoses

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