Health Sciences Centre, Memorial University of Newfoundland, 300 Prince Phillip Drive, St. John's, NL, A1B 3V6, Canada.
Division of Gastroenterology, University of British Columbia, Gordon & Leslie Diamond Health Care Centre, 2775 Laurel Street, Vancouver, BC, V5Z 1M9, Canada.
BMC Gastroenterol. 2022 Apr 11;22(1):181. doi: 10.1186/s12876-022-02253-6.
Emphysematous cystitis (EC) is characterized by the presence of air within the bladder wall, often a complication of urinary tract infection (UTI) by gas-producing organisms. However, EC has also been reported in the setting of infectious colitis suggesting an alternate etiology. We report a rare case of EC in the setting of severe Crohn's colitis with no clinical evidence of UTI.
A 43-year old female presented with a 2-month history of bloody diarrhea consisting of 8-12 bowel movements a day, weight loss of 10 kg and peripheral edema. She also had multiple ulcerated lesions on her abdominal wall and in the perianal region. Initial CT scan was significant for pancolitis, anasarca and EC. The follow-up CT cystogram, flexible cystoscopy and pelvic MRI confirmed the diagnosis of EC and ruled out any fistulous tracts in the pelvis including enterovesical/colovesical fistula. The patient did not report any urinary symptoms and the urinalysis was within normal limits. An extensive infectious workup was negative. Despite the paucity of infectious findings, the EC was empirically treated with an intravenous third-generation cephalosporin. Colonoscopy was significant for multiple ulcerated and hyperemic areas with pseudopolyps all throughout the right, transverse and left colon. Biopsies confirmed Crohn's colitis with no evidence of granulomata or dysplasia. Immunohistochemistry was negative for CMV. The perianal and abdominal wall lesions were suspected to be pyoderma gangrenosum although biopsies were equivocal. The colitis was initially treated with intravenous steroids followed by biologic therapy with Infliximab. Despite appropriate escalation of therapies, the patient developed colonic perforation requiring subtotal colectomy.
This is a rare case of EC in a patient with severe Crohn's colitis. There was no evidence of urinary tract infection or fistulising disease. According to our review, this is the first reported incident of EC in a patient with inflammatory bowel disease without any prior intra-abdominal surgeries. While active Crohn's disease alone is a critical illness, we conclude that concomitant EC may be a poor prognostic factor.
气肿性膀胱炎(EC)的特征是膀胱壁内存在气体,通常是产气生物体引起的尿路感染(UTI)的并发症。然而,EC 也已在感染性结肠炎的情况下报告,提示存在另一种病因。我们报告了一例罕见的严重克罗恩病合并 EC 的病例,无 UTI 的临床证据。
一名 43 岁女性,有 2 个月的血便史,每天排便 8-12 次,体重减轻 10 公斤,外周水肿。她的腹壁和肛周还有多个溃疡性病变。最初的 CT 扫描显示全结肠炎、全身水肿和 EC。后续的 CT 膀胱造影、软性膀胱镜检查和盆腔 MRI 证实了 EC 的诊断,并排除了盆腔内任何瘘管,包括肠膀胱/结肠膀胱瘘。患者没有报告任何尿路症状,尿液分析在正常范围内。广泛的感染性检查均为阴性。尽管缺乏感染性发现,但 EC 仍被经验性地用第三代头孢菌素静脉治疗。结肠镜检查显示整个右半结肠、横结肠和左半结肠均有多个溃疡性和充血性区域,伴有假息肉。活检证实为克罗恩病,无肉芽肿或发育不良的证据。免疫组化检查 CMV 为阴性。肛周和腹壁病变被怀疑为坏疽性脓皮病,尽管活检结果不确定。最初,该结肠炎采用静脉注射类固醇治疗,然后采用英夫利昔单抗进行生物治疗。尽管适当升级了治疗方案,但患者仍出现结肠穿孔,需要进行次全结肠切除术。
这是一例严重克罗恩病合并 EC 的罕见病例。无尿路感染或瘘管性疾病的证据。根据我们的回顾,这是首例报道的无先前腹部手术的炎症性肠病合并 EC 的病例。虽然活动性克罗恩病本身就是一种严重疾病,但我们的结论是,同时合并 EC 可能是预后不良的因素。