A case of chylothorax due to diffuse large B-Cell lymphoma

F. Şahin
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Abstract

A 66-year-old male patient with was admitted to hospital with complaints of fatigue and shortness of breath. In the chest X-ray of the patient, homogeneous density increase was observed in the lower zone of the right lung, suggesting pleural effusion and showing Damoiseau's line. In the patient who underwent thoracentesis, pleural fluid in the form of yellow pus and empyema was seen. The pleural fluid biochemistry was in the character of exudate. Thoracic computed tomography (CT) was performed in the patient who underwent closed underwater drainage with tube thoracostomy. Pleural effusion was reaching 8 cm. in the right hemithorax. The size of the spleen was increased, the liver parenchyma was heterogeneous. In the follow-ups, although the pleural effusion and Damoiseau line of the patient were erased, the fluid continued to come out of the drain as a daily empyema; the patient's clinical and laboratory tests were not compatible with empyema. In addition, a possible hematological malignancy was considered due to low Hb, leukocyte, platelet levels, and hepatosplenomegaly. Chylothorax was taken into the differential diagnosis and triglyceride and cholesterol were sent from the pleural fluid. Triglyceride was high in pleural fluid. No malignant cells were seen in pleural fluid cytology. Positron emission tomography (PET)/CT was performed to determine the etiology in the patient who was diagnosed with chylothorax. There were dense hypermetabolic lymphadenopathy masses starting from the level of the 8th thoracic vertebra up to the retrocrural area in the prevertebral area. Spleen sizes were increased and there were intense hypermetabolic involvements. Involvement due to lymphoproliferative diseases was considered in the foreground. Mediastinoscopy was performed. Biopsies were taken from mass in the paraesophageal area (posterior mediastinum). The pathology result of the biopsies was "Diffuse Large B-Cell Lymphoma". The patient was referred to hematology and oncology clinics for treatment and discharged.
弥漫性大b细胞淋巴瘤致乳糜胸1例
66岁男性患者因疲劳和呼吸短促而入院。患者胸片示右肺下区均匀密度增高,提示胸腔积液,呈达莫瓦索线。在接受胸腔穿刺术的患者中,可见黄色脓液形式的胸腔积液和脓肿。胸膜液生化特征为渗出物。对行闭式水下引流管开胸术的患者行胸部CT检查。胸腔积液达8厘米。在右半胸。脾脏体积增大,肝脏实质不均匀。在随访中,虽然患者的胸膜积液和达摩索线已被清除,但液体继续从引流管中流出,成为每日的脓胸;病人的临床和实验室检查与脓胸不符。此外,由于低血红蛋白、白细胞、血小板水平和肝脾肿大,可能存在血液系统恶性肿瘤。乳糜胸纳入鉴别诊断,胸膜液检测甘油三酯和胆固醇。胸膜液中甘油三酯含量高胸膜液细胞学检查未见恶性细胞。诊断为乳糜胸的患者行正电子发射断层扫描(PET)/CT以确定病因。椎前区从第8胸椎水平至脚后可见密集的高代谢性淋巴结肿物。脾脏体积增大,伴有强烈的高代谢累及。由于淋巴增生性疾病的累及被认为是前景。行纵隔镜检查。食道旁区(后纵隔)肿块活检。活检病理结果为“弥漫性大b细胞淋巴瘤”。患者转诊至血液科及肿瘤科治疗后出院。
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