Moh M, et al. - An assessment was performed of the angiomyomatous hamartoma of lymph nodes (AMH-LN) for clinical, morphologic and immunophenotypic features of lymph nodes (LN)-lymphangioleiomyomatosis (LAM). It was determined that neither of the cases displayed classical features of LN-LAM such as subcapsular localization, extranodal extension, intralymphatic growth, compact nests, branching lymphatic channels, plump cell shape or foamy/clear cytoplasm. None exhibited any staining for cathepsin K, HMB45, or MiTF. No clinical, morphologic or immunohistochemical evidence was reported to suggest that AMH-LN as being a variant of LN-LAM.