原发性肺淋巴瘤伴上腔静脉综合征

A. Rosyid, Resti Yudhawati Meliana
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摘要

原发性肺淋巴瘤(PPL)是一种淋巴样细胞的克隆性增生,累及一个或两个肺(实质和/或支气管)。PPL在所有淋巴瘤病例中约占0.4%,在NHL病例中占3.6%。I期和II期5年生存率为90%,III期和IV期为80%。一名63岁男性农民,入院前主诉为呼吸短促1周,咳嗽1个月,食欲不振,盗汗。右侧胸部体检异常,右侧锁骨上及颈部无压痛性淋巴结肿大,上腔静脉综合征。CT引导下FNAB提示NHL。患者采用CHOP化疗方案。然而,对于高级别淋巴瘤,患者的反应并不好。
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Primary Pulmonary Lymphoma with Superior Vena Cava Syndrome
Primary Pulmonary Lymphoma (PPL) is a clonal proliferation of lymphoid cells that involve one or two lungs (parenchyma and or bronchi. PPL is found in approximately 0.4% of all lymphoma cases and 3.6% of NHL cases. Five years survival rate at stage I and II is 90%, and 80% in stage III and IV. A 63-year-old male farmer presented with chief complaint of shortness of breath for one week before admission and preceded by coughing for a month, loss of appetite and night sweating. There was an abnormal physical examination on the right side of the chest with non-tender lymph node enlargements in the right supraclavicular and neck region and superior vena cava syndrome. CT guided FNAB suggesting NHL. Patient was treated with CHOP chemotherapy regiment. However, with high grade lymphoma, patient did not respond well.
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