Department of Internal Medicine, Kaiser Permanente Santa Clara, Santa Clara, CA, USA.
Department of Pathology, Kaiser Permanente Santa Clara, Santa Clara, CA, USA.
Perm J. 2022 Apr 5;26(1):132-136. doi: 10.7812/TPP/21.070.
Mixed phenotype acute leukemia (MPAL) is a rare type of acute leukemia with immunophenotypic features of both myeloid-derived and lymphoid-derived lineages.
We present an atypical case of a 32-year-old woman presenting with an anterior mediastinal mass and pericardial/pleural involvement that was initially diagnosed as primary mediastinal diffuse large B-cell lymphoma. However, flow cytometry on pleural fluid confirmed the diagnosis of MPAL of B-cell/myeloid lineage without peripheral blood/bone marrow involvement. The patient was treated with an acute lymphoblastic leukemia-type regimen and proceeded with myeloablative allogeneic hematopoietic cell transplantation in first complete remission.
MPAL can rarely present with isolated extramedullary disease without leukemic involvement and can often be misdiagnosed as a non-Hodgkin lymphoma. Careful integration of all the clinical data, particularly flow cytometry results, can clarify the diagnosis and change the treatment plan.
混合表型急性白血病(MPAL)是一种罕见的急性白血病,具有髓系和淋巴系来源的免疫表型特征。
我们报告了一例 32 岁女性的不典型病例,该患者表现为前纵隔肿块和心包/胸膜受累,最初诊断为原发性纵隔弥漫性大 B 细胞淋巴瘤。然而,胸腔积液的流式细胞术证实了 B 细胞/髓系谱系的 MPAL 诊断,无外周血/骨髓受累。该患者接受了急性淋巴细胞白血病样方案治疗,并在首次完全缓解后进行了清髓性异基因造血细胞移植。
MPAL 可罕见地表现为孤立性骨髓外疾病而无白血病累及,且常被误诊为非霍奇金淋巴瘤。仔细综合所有临床数据,特别是流式细胞术结果,可明确诊断并改变治疗方案。