Key result
The MYD88 L265P mutation was identified in the lesional skin of cutaneous Waldenström macroglobulinemia.
Single-case data warrant no practice change; leaves open MYD88 L265P's role in cutaneous Waldenström macroglobulinemia.
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Shibuya et al. (2026) studied this question. The MYD88 L265P mutation was identified in the lesional skin of cutaneous Waldenström macroglobulinemia.
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