Khushman M, Morris M I, Diaz L, Goodman M, Pereira D, Fuller K, Garcia-Buitrago M, Moshiree B, Zelaya S, Nayer A, Benjamin C L, Komanduri K V
The University of South Alabama, Mitchell Cancer Institute, Mobile, Alabama, USA.
Infectious Diseases, The University of Miami Miller School of Medicine, Miami, Florida, USA.
Transplant Proc. 2017 Mar;49(2):373-377. doi: 10.1016/j.transproceed.2016.12.012.
Syndrome of inappropriate anti-diuretic hormone (SIADH) has been reported to be associated with systemic Strongyloides stercoralis. Here, we report a case of a stem cell transplant (SCT) recipient who developed severe SIADH secondary to systemic S Stercoralis. The SIADH resolved quickly after treating the systemic S Stercoralis with ivermectin. A systematic review of the literature was performed by PubMed, Scopus, and Cochrane database search. Only eight cases of S Stercoralis in allogeneic SCT recipients have been previously reported. To our knowledge, ours is the first reported case of SIADH secondary to S Stercoralis infection in an allogeneic SCT recipient. Prior to transplantation, even if asymptomatic, patients from endemic regions should be screened with strongyloides immunoglobulin (Ig)G serology. Pretransplantation eosinophilia should be evaluated by screening multiple stool samples for ova and parasites. Transplant candidates with positive serology or stool tests can be treated pretransplantation to eradicate infection. Patients at risk for S Stercoralis who develop nonspecific gastrointestinal complaints, rash, pulmonary infiltrates, or gram-negative bacteremia or meningitis may have S Stercoralis hyperinfection syndrome. Our case indicates that the development of SIADH may be an additional clue to this diagnosis. Appropriate diagnostic studies, including repeat stool and other body fluid sampling, should be expedited and ivermectin therapy initiated rapidly to prevent significant morbidity and mortality.
抗利尿激素分泌异常综合征(SIADH)已被报道与系统性粪类圆线虫感染有关。在此,我们报告一例干细胞移植(SCT)受者,其因系统性粪类圆线虫感染继发严重SIADH。在用伊维菌素治疗系统性粪类圆线虫感染后,SIADH迅速缓解。通过PubMed、Scopus和Cochrane数据库检索对文献进行了系统回顾。此前仅报道过8例同种异体SCT受者发生粪类圆线虫感染的病例。据我们所知,我们的病例是首例报道的同种异体SCT受者因粪类圆线虫感染继发SIADH的病例。移植前,即使无症状,来自流行地区的患者也应进行粪类圆线虫免疫球蛋白(Ig)G血清学筛查。应通过多次粪便样本检查虫卵和寄生虫来评估移植前嗜酸性粒细胞增多情况。血清学或粪便检测呈阳性的移植候选者可在移植前接受治疗以根除感染。有粪类圆线虫感染风险且出现非特异性胃肠道症状、皮疹、肺部浸润或革兰氏阴性菌血症或脑膜炎的患者可能患有粪类圆线虫高度感染综合征。我们的病例表明,SIADH的发生可能是该诊断的另一条线索。应加快进行适当的诊断研究,包括重复粪便和其他体液采样,并迅速开始伊维菌素治疗,以防止出现严重的发病率和死亡率。