Sritharan Shobashenee, Lau Peter Sie-Teck, Manan Kamilah, Mohan Anand
Department of Pediatrics, Bintulu Hospital, Ministry of Health Malaysia, Bintulu, Malaysia.
Department of Radiology, Bintulu Hospital, Ministry of Health Malaysia, Bintulu, Malaysia.
Front Pediatr. 2023 Jul 13;11:1214551. doi: 10.3389/fped.2023.1214551. eCollection 2023.
Systemic lupus erythematosus (SLE) can involve any organ system and cause a wide range of manifestations. Noninfectious inflammatory lesions termed aseptic abscesses have been reported in some autoimmune and autoinflammatory conditions but not in childhood-onset SLE. In this report, we highlight the unusual finding of occult splenic abscesses in two children diagnosed with SLE who had no evidence of concomitant infection.
An 8-year-old and an 11-year-old were admitted separately to the hospital with fever for 7 and 14 days, respectively. In the younger child, a generalized rash preceded the fever. Both had been well, with no significant past medical history prior to the onset of the illness. In both girls, abdominal ultrasonography showed multiple small hypoechoic lesions suggestive of abscesses scattered throughout the spleen. Their C-reactive protein and blood cultures were negative, and symptoms persisted despite intravenous antibiotics. Fulfilling the clinical and immunologic criteria for diagnosis, both were ultimately diagnosed with childhood-onset SLE. Rapid recovery of symptoms and complete resolution of the abscesses ensued with corticosteroids and immunosuppressive therapy.
These two cases suggest that aseptic splenic abscesses may occur in childhood-onset SLE. Autoimmune conditions such as SLE should be included in the differential diagnosis of children with occult splenic abscesses.
系统性红斑狼疮(SLE)可累及任何器官系统并引发广泛的临床表现。在一些自身免疫性和自身炎症性疾病中已报道过称为无菌性脓肿的非感染性炎性病变,但儿童期发病的SLE中未见报道。在本报告中,我们着重介绍了两名诊断为SLE的儿童中隐匿性脾脓肿这一不寻常的发现,他们没有合并感染的证据。
一名8岁和一名11岁儿童分别因发热7天和14天入院。在年幼的儿童中,发热前出现全身性皮疹。两人在发病前均健康,无重大既往病史。两名女孩的腹部超声均显示多个小的低回声病变,提示脓肿散在分布于整个脾脏。她们的C反应蛋白和血培养均为阴性,尽管使用了静脉抗生素,症状仍持续存在。根据诊断的临床和免疫学标准,两人最终均被诊断为儿童期发病的SLE。使用皮质类固醇和免疫抑制治疗后,症状迅速缓解,脓肿完全消退。
这两例病例提示无菌性脾脓肿可能发生于儿童期发病的SLE。自身免疫性疾病如SLE应纳入隐匿性脾脓肿患儿的鉴别诊断。