Gastroenterology, Barnet and Chase Farm Hospitals NHS Trust, London, UK
Gastroenterology, University College London Hospitals NHS Foundation Trust, London, UK.
BMJ Case Rep. 2023 Sep 26;16(9):e254073. doi: 10.1136/bcr-2022-254073.
Seronegative villous atrophy (SNVA) is a diagnostic challenge for gastroenterologists, which is defined by villous atrophy and negative coeliac serology. Non-coeliac forms of SNVA, such as autoimmune enteropathy, can be life-threatening leading to intractable diarrhoea and severe malabsorption that require systemic immunosuppression. When all known causes have been excluded, it is termed idiopathic villous atrophy (IVA). We present a case of non-coeliac SNVA complicated by Kaposi sarcoma (KS). A previously well HIV-negative man in his 30s presented with a 4-month history of watery diarrhoea and 25 kg weight loss. After prolonged investigation, he was diagnosed with non-coeliac SNVA without an identified aetiology that would be consistent with IVA. Clinical recovery was achieved with parenteral nutrition for type II intestinal failure and immunosuppression using high-dose corticosteroids. On subsequent gastroscopy, he was diagnosed with localised intestinal KS prompting cessation of all immunosuppression but remained in clinical remission.
血清阴性绒毛萎缩症(SNVA)是消化科医生面临的诊断难题,其定义为绒毛萎缩和阴性乳糜泻血清学。非乳糜泻形式的 SNVA,如自身免疫性肠炎,可能危及生命,导致难治性腹泻和严重吸收不良,需要全身免疫抑制。当排除所有已知原因时,称为特发性绒毛萎缩症(IVA)。我们报告了一例非乳糜泻 SNVA 合并卡波西肉瘤(KS)的病例。一名 30 多岁的既往健康的 HIV 阴性男性,出现 4 个月的水样腹泻和 25kg 体重减轻。经过长时间的检查,他被诊断为非乳糜泻 SNVA,没有明确的病因,符合 IVA。通过 II 型肠衰竭的肠外营养和大剂量皮质类固醇的免疫抑制治疗,他实现了临床康复。随后的胃镜检查诊断为局部肠道 KS,促使停止所有免疫抑制治疗,但仍处于临床缓解期。