Clinical laboratory · 2025
Lymphoplasmacytic Lymphoma with IgA Paraprotein: a Case Report and Literature Review.
СтатьяКлинический случайОбзорНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Sun Yingying, Li Liyan, Jiang Fengjuan, Liu Hui, Gao Shan, Wang Honglei, Ren Yue, Song Jia, Wang Huaquan, Shao Zonghong, Fu Rong, Li Lijuan
Аннотация
BACKGROUND: Lymphoplasmacytic Lymphoma (LPL) with immunoglobulin (Ig)A paraprotein is rare. When plasma cells dominate, the diagnosis becomes more challenging.
METHODS: We reported a case of a 71-year-old male with elevated creatinine, splenomegaly, monoclonal IgA, and MYD88 mutation. Only monoclonal plasma cells were detected first, leading to a misdiagnosis of multiple myeloma. When progressive spleen enlargement was observed, re-evaluation revealed the emergence of monoclonal lymphocytes and the diagnosis was revised to LPL.
RESULTS: The addition of rituximab to DVD regimen led to a partial response.
CONCLUSIONS: For cases where an initial definitive diagnosis cannot be established, close follow-up is required for timely diagnosis revision and therapeutic adjustment.
METHODS: We reported a case of a 71-year-old male with elevated creatinine, splenomegaly, monoclonal IgA, and MYD88 mutation. Only monoclonal plasma cells were detected first, leading to a misdiagnosis of multiple myeloma. When progressive spleen enlargement was observed, re-evaluation revealed the emergence of monoclonal lymphocytes and the diagnosis was revised to LPL.
RESULTS: The addition of rituximab to DVD regimen led to a partial response.
CONCLUSIONS: For cases where an initial definitive diagnosis cannot be established, close follow-up is required for timely diagnosis revision and therapeutic adjustment.