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Severe aplastic anemia concurrent with lymphoplasmacytic lymphoma/Waldenström's macroglobulinemia: A case report.

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Internal medicine (Tokyo, Japan) 📖 저널 OA 81.2% 2024: 6/6 OA 2025: 37/56 OA 2026: 76/84 OA 2024~2026 2026 OA
Retraction 확인
출처

Okuda T, Hanyu Y, Mineshige H, Inoue Y, Sakurada M, Matsui M

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A 79-year-old female presented with progressive dyspnea.

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APA Okuda T, Hanyu Y, et al. (2026). Severe aplastic anemia concurrent with lymphoplasmacytic lymphoma/Waldenström's macroglobulinemia: A case report.. Internal medicine (Tokyo, Japan). https://doi.org/10.2169/internalmedicine.6790-25
MLA Okuda T, et al.. "Severe aplastic anemia concurrent with lymphoplasmacytic lymphoma/Waldenström's macroglobulinemia: A case report.." Internal medicine (Tokyo, Japan), 2026.
PMID 41813169 ↗

Abstract

A 79-year-old female presented with progressive dyspnea. A bone marrow biopsy revealed hypoplastic marrow with abnormal lymphoid cells. A genetic analysis revealed a MYD88 p.V204F mutation, supporting the diagnosis of lymphoplasmacytic lymphoma/Waldenström's macroglobulinemia (LPL/WM). Additional evaluations established a concomitant diagnosis of aplastic anemia (AA). Treatment prioritized AA with cyclosporine and eltrombopag. Subsequently, the LPL/WM was treated with rituximab monotherapy. This sequential treatment resulted in a symptomatic improvement. Although AA is a diagnosis of exclusion, its coexistence with lymphoma is rare. This case highlights the diagnostic and therapeutic complexity of AA and LPL/WM overlap and suggests that prioritizing the treatment of AA may lead to better outcomes.

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