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- W2144268455 abstract "Multinucleate cell angiohistiocytoma (MCAH) is a rare, benign vascular proliferation. Fewer than 80 cases have been reported to date, which may relate to under-recognition of this entity. Lesions are commonly asymptomatic and appear as erythematous to violaceous papules on the lower extremities and dorsal hands of middle-aged to elderly women. The characteristic histopathologic and immunohistochemical features of MCAH are essential for definitive diagnosis of MCAH. Multinucleate cell angiohistiocytoma follows a slowly progressive course, although spontaneous regression has been reported in rare cases. We present a case of MCAH to increase awareness and elucidate the characteristic clinical and histopathologic features of this disorder." @default.
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- W2144268455 date "2014-01-01" @default.
- W2144268455 modified "2023-10-14" @default.
- W2144268455 title "Multinucleate cell angiohistiocytoma: a case report and review of the literature." @default.
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- W2144268455 doi "https://doi.org/10.5070/d3205022610" @default.
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