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Primary plasmacytoma involving mediastinal lymph nodes: A diagnostic mimicry of primary mediastinal lymphoma

机译:涉及纵隔淋巴结的原发性浆细胞瘤:原发性纵隔淋巴瘤的诊断模仿

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Plasmacytomas could involve any organ, and at times might pose a diagnostic challenge when the site of involvement is unusual, or if the presentation is similar to other diseases. We describe a 48-year-old man presenting with worsening shortness of breath and chest discomfort with radiologic evidence of mediastinal enlargement, mimicking a lymphoma with mediastinal involvement. An excisional biopsy of a mediastinal lymph node showed a plasma-cell infiltrate strongly positive for CD138, with a flow-cytometry analysis showing a population of lambda-restricted neoplastic plasma cells. He failed to respond to 50Gy involved-field radiotherapy, but achieved a partial response to combination chemotherapy. He underwent high-dose chemotherapy with melphalan (200mg/m^2) followed by lenalidomide maintenance, and is in complete remission 18months postautografting. This case illustrates a unique and rare presentation of primary lymph-node plasmacytomas involving the mediastinum potentially mistaken as lymphoid malignancy. Clinicians should be aware of the plasma-cell origin of the mediastinal neoplastic process.
机译:浆细胞瘤可累及任何器官,有时在累及部位异常或呈与其他疾病相似的情况下,有时可能会给诊断带来挑战。我们描述了一个48岁的男性,表现为呼吸急促和胸部不适加重,放射学证据显示纵隔肿大,模仿了纵隔累及的淋巴瘤。纵隔淋巴结的切除活检显示,CD138的浆细胞浸润强烈阳性,流式细胞术分析显示有λ限制的赘生性浆细胞。他对50Gy累及野放疗没有反应,但对联合化疗取得了部分反应。他接受了美法仑(200mg / m ^ 2)的大剂量化疗,并接受来那度胺维持治疗,并且自体移植后18个月完全缓解。该病例说明涉及纵隔的原发性淋巴结浆细胞瘤的独特且罕见的表现,可能被误认为是淋巴样恶性肿瘤。临床医生应注意纵隔肿瘤过程的浆细胞起源。

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