Daniel Alexandra, Bagnato Gianluca, Vital Edward, Del Galdo Francesco
Department of Rheumatology Unit, Centro Hospitalar e Universitario de Coimbra EPE, Coimbra, Portugal.
Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK.
BMJ Case Rep. 2017 Oct 20;2017:bcr-2017-222339. doi: 10.1136/bcr-2017-222339.
The authors present a case of a 51-year-old woman with clinical diagnosis of mixed connective tissue disease and overlap systemic lupus erythematosus features, with a 6-month history of progressive painless abdominal distension. On examination, evident signs of ascites were present. Both the abdominal-pelvic ultrasound and CT scan confirmed a large amount of ascites. A diagnostic paracentesis was performed, which revealed typical features of chylous ascites (CA). An extensive diagnostic work-up led by a multidisciplinary team was performed, excluding malignancy, cirrhosis, infectious, as well as cardiac and primary lymphatic causes. The patient was kept under surveillance, with dietary therapy and periodic ascitic drainages. The hypothesis of an autoimmune cause for CA was considered by exclusion. Rituximab therapy was initiated and an excellent response was achieved, with reduction of the rate of accumulation of CA and an increase in quality of life of the patient.
作者报告了一例51岁女性病例,临床诊断为混合性结缔组织病并伴有重叠系统性红斑狼疮特征,有6个月进行性无痛性腹胀病史。检查时发现明显的腹水体征。腹部盆腔超声和CT扫描均证实有大量腹水。进行了诊断性腹腔穿刺术,结果显示为典型的乳糜性腹水(CA)特征。由多学科团队主导进行了广泛的诊断性检查,排除了恶性肿瘤、肝硬化、感染以及心脏和原发性淋巴系统病因。对患者进行监测,采用饮食疗法并定期进行腹水引流。通过排除法考虑CA的自身免疫性病因。开始使用利妥昔单抗治疗,取得了良好效果,CA的积聚速率降低,患者生活质量提高。