Abdulfattah Omar, Rahman Ebad Ur, Bhattarai Bikash, Dahal Sumit, Alnafoosi Zainab, Trauber David, Enriquez Danilo, Schmidt Frances
Medicine Department, Pulmonary and Critical Care Division, Interfaith Medical Center, Brooklyn, NY, USA.
Medicine Department, Interfaith Medical Center, Brooklyn, NY, USA.
J Community Hosp Intern Med Perspect. 2018 Apr 17;8(2):68-72. doi: 10.1080/20009666.2018.1440854. eCollection 2018.
: Lymphoplasmacytic lymphoma (LPL) is a mature B cell lymphoma that usually involves the bone marrow, spleen and lymph nodes. Extramedullary involvement, including the lung, is rarely reported. : A 73-year-old female initially presented to our hospital complaining of productive cough of white-colour sputum for three weeks duration. She reported unintentional weight loss of ten pounds over the last five months. There was no history of haemoptysis, fever, night sweats, chills, recent infections or hospitalization. Chest imaging showed right lower lobe consolidation, small right pleural effusion. She was treated with oral antibiotic for pneumonia. After two months, a follow up chest imaging revealed persistent right lower lobe consolidation. Therefore, she was worked up for the possibility of malignancy. Bronchoscopy showed polypoid nodularities surrounded by black discoloured mucosa in the sub-segmental bronchi of the right lower lobe, and biopsy specimen revealed atypical B cell lymphocytic infiltrate. Polymerase chain reaction confirmed a clonal B-cell gene rearrangement supportive for a low-grade B-cell Lymphoma. Subsequently; serum immunofixation showed IgM of 1491 mg/dL (normal range 26-217 mg/dl) with normal levels of IgG and IgA. Urine contained free kappa light chains. Cytology with immunophenotyping of pleural fluid revealed lymphoplasmacytic lymphocytes. This combination of lab and bronchoscopy findings established the diagnosis of extramedullary Waldenström's macroglobulinemia. : Waldenström's macroglobulinemia, a manifestation of LPL, is associated with an IgM monoclonal gammopathy in the blood. Extramedullary involvement including the lung is rarely seen in LPL. Physicians need to be aware of this rare presentation.
淋巴浆细胞淋巴瘤(LPL)是一种成熟B细胞淋巴瘤,通常累及骨髓、脾脏和淋巴结。髓外受累,包括肺部受累,鲜有报道。
一名73岁女性最初因持续三周的白色咳痰前来我院就诊。她自述在过去五个月中体重无意减轻了10磅。无咯血、发热、盗汗、寒战、近期感染或住院史。胸部影像学检查显示右下叶实变,右侧少量胸腔积液。她接受了口服抗生素治疗肺炎。两个月后,胸部影像学复查显示右下叶实变持续存在。因此,对其进行了恶性肿瘤可能性的评估。支气管镜检查显示右下叶亚段支气管内有息肉样结节,周围黏膜呈黑色,活检标本显示非典型B细胞淋巴细胞浸润。聚合酶链反应证实了支持低度B细胞淋巴瘤的克隆性B细胞基因重排。随后,血清免疫固定电泳显示IgM为1491mg/dL(正常范围26 - 217mg/dl),IgG和IgA水平正常。尿液中含有游离κ轻链。胸腔积液的细胞学及免疫表型分析显示为淋巴浆细胞淋巴细胞。实验室检查结果与支气管镜检查结果相结合,确诊为髓外华氏巨球蛋白血症。
华氏巨球蛋白血症是LPL的一种表现形式,与血液中的IgM单克隆丙种球蛋白病相关。LPL中很少见包括肺部在内的髓外受累情况。医生需要了解这种罕见的表现形式。