Desailloud R, Papo T, Vaneecloo S, Gamblin C, Vanhille P, Piette J C
Centre Hospitalier de Valenciennes, France.
Arthritis Rheum. 1998 Jul;41(7):1318-20. doi: 10.1002/1529-0131(199807)41:7<1318::AID-ART24>3.0.CO;2-K.
A 29-year-old woman was referred for abdominal pain. Results of tests for lupus anticoagulant and antibodies to phosphatidylserine and to beta2-glycoprotein I were positive, but the patient had no features of systemic lupus erythematosus (SLE). Abdominal ultrasonography showed a thickening of the gallbladder wall without cholelithiasis. A surgical procedure revealed necrotic areas of the gallbladder wall, and a cholecystectomy was performed. Histologic examination of the gallbladder showed multiple thrombi and no vasculitis. Despite full-dose heparin, the patient developed a catastrophic antiphospholipid syndrome (APS) and subsequently died. Among connective tissue disorders, acute acalculous cholecystitis has been reported in patients with polyarteritis nodosa and/or SLE. APS should be considered as a possible cause of acalculous cholecystitis.
一名29岁女性因腹痛前来就诊。狼疮抗凝物、抗磷脂酰丝氨酸抗体及抗β2糖蛋白I抗体检测结果均为阳性,但该患者并无系统性红斑狼疮(SLE)的特征表现。腹部超声显示胆囊壁增厚但无胆结石。手术过程中发现胆囊壁有坏死区域,遂进行了胆囊切除术。胆囊组织学检查显示有多处血栓形成且无血管炎表现。尽管给予了全剂量肝素治疗,该患者仍发展为灾难性抗磷脂综合征(APS),随后死亡。在结缔组织疾病中,结节性多动脉炎和/或SLE患者曾有急性非结石性胆囊炎的报道。APS应被视为非结石性胆囊炎的一个可能病因。