Simopoulou Theodora, Klimopoulos Serafim, Sampaziotis Dimitrios, Tzortziotis Apostolos, Bogdanos Dimitrios, Sakkas Lazaros I
Department of Rheumatology and Clinical Immunology, Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa, Greece.
2nd Department of Surgery, Evangelismos General Hospital, Athens, Greece.
J Scleroderma Relat Disord. 2018 Oct;3(3):NP1-NP6. doi: 10.1177/2397198318764793. Epub 2018 Mar 26.
IgG4-related disease is an immune-mediated deposition of fibro-inflammatory tissue with IgG4-positive plasma cells and dense fibrosis in a single or multiple organs. It often raises concern for malignancy requiring biopsy for diagnosis. Presentation may vary according to organ involved. IgG4-related retroperitoneal fibrosis accounts for two-thirds of the previously considered idiopathic retroperitoneal fibrosis cases. In IgG4-related retroperitoneal fibrosis, computed tomography scan or magnetic resonance imaging shows periaortic soft tissue that extends from below the kidneys to iliac arteries and entrap ureters causing hydronephrosis and renal failure. We present a rare case of IgG4-related retroperitoneal fibrosis presenting with leg swelling and pain due to inferior vena cava compression and thrombosis, and we review current concepts on disease pathogenesis, diagnosis and treatment.
IgG4相关性疾病是一种免疫介导的纤维炎症组织沉积,在单个或多个器官中存在IgG4阳性浆细胞和致密纤维化。它常常引发对恶性肿瘤的担忧,需要进行活检以明确诊断。临床表现可能因受累器官而异。IgG4相关性腹膜后纤维化占既往认为的特发性腹膜后纤维化病例的三分之二。在IgG4相关性腹膜后纤维化中,计算机断层扫描或磁共振成像显示主动脉周围软组织从肾下延伸至髂动脉,并压迫输尿管导致肾积水和肾衰竭。我们报告一例罕见的IgG4相关性腹膜后纤维化病例,该病例因下腔静脉受压和血栓形成出现腿部肿胀和疼痛,并对疾病的发病机制、诊断和治疗的当前概念进行综述。