Yokoyama Hiroki, Sakaguchi Mayumi, Yamada Yuko, Kitamoto Koichi, Okada Shinichi, Kanzaki Susumu, Namba Noriyuki
Division of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, Yonago, Japan.
Department of Pediatrics, Tottori Prefectural Central Hospital, Tottori, Japan.
Front Pediatr. 2020 Jun 2;8:216. doi: 10.3389/fped.2020.00216. eCollection 2020.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic disease causing renal cysts. Reports on kidney cyst infection in children are rare despite cyst infections being important complications of ADPKD. Here, we report a case of a child without any medical history who had a urinary tract infection with sepsis at 7 months. Leukocyturia persisted despite antibiotic therapy because the infection was treatment-resistant. Initial ultrasound and contrast computed tomography were inconclusive because cysts could not be detected clearly, and a family history of renal cysts was not determined. Subsequently, history of paternal renal cysts, thick walls in infectious cystic lesions on diffusion-weighted magnetic resonance imaging (MRI), and multiple small lesions with high signals on T2-weighted imaging in both kidneys became apparent. Upon diagnosis of ADPKD with cyst infection, antibiotic therapy was switched from cefotaxime to trimethoprim/sulfamethoxazole to achieve better cyst penetration, which successfully resolved the infection. In this patient, MRI was effective for clear visualization and diagnosis of infectious lesions and small cysts in undiagnosed ADPKD with cyst infection. Administering antibiotics with better cyst penetration is important. Trimethoprim/sulfamethoxazole is an option for use in children. This is the first case report that describes ADPKD with cyst infection in an infant in detail.
常染色体显性多囊肾病(ADPKD)是导致肾囊肿的最常见遗传性疾病。尽管囊肿感染是ADPKD的重要并发症,但关于儿童肾囊肿感染的报道却很少。在此,我们报告一例7个月大的无任何病史的儿童,其患有尿路感染并伴有败血症。尽管进行了抗生素治疗,但白细胞尿仍持续存在,因为该感染具有耐药性。最初的超声和增强计算机断层扫描结果不明确,因为囊肿无法清晰检测到,且未确定肾囊肿家族史。随后,父亲的肾囊肿病史、扩散加权磁共振成像(MRI)上感染性囊性病变的厚壁以及双肾T2加权成像上多个高信号小病变变得明显。在诊断为ADPKD合并囊肿感染后,抗生素治疗从头孢噻肟改为甲氧苄啶/磺胺甲恶唑,以实现更好的囊肿穿透,从而成功解决了感染问题。在该患者中,MRI对于清晰显示和诊断未确诊的合并囊肿感染的ADPKD中的感染性病变和小囊肿有效。使用具有更好囊肿穿透性的抗生素很重要。甲氧苄啶/磺胺甲恶唑是儿童使用的一种选择。这是第一例详细描述婴儿ADPKD合并囊肿感染的病例报告。