Li Ning, Wang Jun C, Zhu Ming H, Wang Jia Y, Fu Xue L, Zhou Jie R, Zheng Song G, Han Jie, Chan Paul
Department of Rheumatology, Shanghai East Hospital, Tongji University, Shanghai, China.
Int J Clin Exp Pathol. 2013;6(2):273-80. Epub 2013 Jan 15.
Systemic lupus erythematosus (SLE) is a common autoimmune disease that involved multiple organ systems. Diagnosis is usually not difficult. However, SLE involved spleen with spontaneous rupture is a rare condition that has been only 5 cases reported previously; and no definite pathologic diagnosis has been reported. We present the case of a 54 year-old white American woman who had SLE for 10 years with multiple immunosuppressive agents treatment at stable condition. She had acute abdomen presented to the emergency department and received timely surgical treatment which confirmed she had spontaneous spleen rupture (SSR). Detailed pathologic study, with control of a traumatic rupture spleen of almost the same age and sex, revealed marked congestion of the red pulp and atrophy of white pulp notified in the SLE spleen. Congestion of red pulp may be the cause of SSR in the SLE spleen.
系统性红斑狼疮(SLE)是一种累及多个器官系统的常见自身免疫性疾病。诊断通常并不困难。然而,SLE累及脾脏并自发破裂是一种罕见情况,此前仅有5例报道;且尚无明确的病理诊断报告。我们报告一例54岁的美国白人女性,她患SLE已10年,在病情稳定时接受了多种免疫抑制剂治疗。她因急腹症就诊于急诊科,接受了及时的手术治疗,证实为自发性脾破裂(SSR)。详细的病理研究,与几乎相同年龄和性别的外伤性破裂脾脏作对照,发现SLE脾脏红髓明显充血,白髓萎缩。红髓充血可能是SLE脾脏发生SSR的原因。