Composite diffuse large B-cell and peripheral T-cell lymphoma with T-helper phenotype treated with both rituximab and brentuximab vedotin
Composite diffuse large B-cell and peripheral T-cell lymphoma with T-helper phenotype treated with both rituximab and brentuximab vedotin
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使用利妥昔单抗和 brentuximab vedotin 治疗的具有 T 辅助表型的复合弥漫性大 B 细胞和外周 T 细胞淋巴瘤
DOI:
10.1007/s00277-021-04633-6
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发表时间:
2021
影响因子:
3.5
通讯作者:
Tajima Katsushi
中科院分区:
文献类型:
--
作者:
Ohya Kouichi;Okuyama Shuhei;Ogata Shin-ya;Maeda Kunihiko;Yamada Kyohei;Ohshima Kouichi;Tajima Katsushi
Composite lymphoma (CL) is defined as two or more distinct lymphoma subtypes in a single anatomic tissue or the same lymph node, while discordant lymphoma is two or more distinct lymphoma subtypes existing at different sites simultaneously [1]. The T-/B-cell type CL is quite rare [2]. Optimal or standard treatments for T-/B-cell type CLs have not yet been defined.An 80-year-old Japanese woman, who had myelodysplastic syndrome with multilineage dysplasia 10 years ago, visited our hospital regularly without any treatments. Her regular examination identified systemic lymph node (LN) enlargements, and after a short time, she developed several subcutaneous nodules. Laboratory findings were as follows: WBCs, 2220/μL; hemoglobin, 11.8 g/dL; Plts, 96,000; soluble IL-2 receptor, 4170 U/mL (normal 121–613). Positronemission tomography/computed tomography (PET-CT) showed increased metabolic activity in the LNs and subcutaneous nodules (Fig. 1a). A supraclavicular LN biopsy revealed the diffuse proliferation of medium to large abnormal lymphoid cells and endothelium in expanded interfollicular areas (Fig. 1b, c). The medium-sized cells in the interfollicular areas were positive for CD3, PD-1, ICOS, CXCL13, and BC-6, but negative for CD10 (Fig. 1d, e). The
影响因子:
3.3
作者:
F. Vega;L. J. Medeiros
通讯作者:
L. J. Medeiros