Hall S, McCormick J L, Greipp P R, Michet C J, McKenna C H
Ann Intern Med. 1985 Mar;102(3):325-8. doi: 10.7326/0003-4819-102-3-325.
Fourteen patients with systemic lupus erythematosus had splenectomies done between 1960 and 1982 for treatment of severe thrombocytopenia. Thrombocytopenia persisted or recurred within 1 month postoperatively in five patients and within 6 months in three others. Three patients had late recurrence (18, 30, and 54 months after splenectomy); in two it was probably related to withdrawal of immunosuppressive agents or corticosteroids. Median lowest platelet count before splenectomy and median platelet count at relapse or failure of splenectomy were both 8000/microL. Only two patients maintained normal platelet counts without need for corticosteroids or other treatment. These results differ from those in patients with idiopathic thrombocytopenic purpura. Other treatments should be tried before splenectomy is done for thrombocytopenia in patients with systemic lupus erythematosus.
1960年至1982年间,14例系统性红斑狼疮患者因严重血小板减少症接受了脾切除术。5例患者术后1个月内血小板减少症持续存在或复发,另外3例在6个月内复发。3例患者出现晚期复发(脾切除术后18、30和54个月);其中2例可能与停用免疫抑制剂或皮质类固醇有关。脾切除术前血小板计数中位数最低值以及脾切除复发或失败时的血小板计数中位数均为8000/微升。只有2例患者无需皮质类固醇或其他治疗即可维持正常血小板计数。这些结果与特发性血小板减少性紫癜患者的结果不同。对于系统性红斑狼疮患者的血小板减少症,在进行脾切除术之前应尝试其他治疗方法。