IntroductionLymph node architecture can be partially replaced in conditions such as lymph node infarction, vascular transformation of the sinuses, bacillary angiomatosis, and metastatic angiosarcoma.1-3 In 1992, Chan et al were the first to report an angiomyomatous hamartoma as an independent condition characterized by replacement of the nodal parenchyma with smooth-muscle cells and fibrous tissue arranged in a sclerotic stroma.4 Angiomyomatous hamartomas have been de
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