Yamauchi F, Tanabe R, Nakashima R, Endoh M, Nomoto Y, Sakai H, Sakonjyu T, Shindoh Y, Kimura N, Takayasu H
Department of: Nephrology and Metabolism, School of Medicine, Tokai University, Kanagawa, Japan.
Tokai J Exp Clin Med. 1995 Dec;20(4-6):233-40.
We treated a 55-year-old male patient with Wegener's granulomatosis (WG) associated with frequent gastric bleeding from multiple ulcerative lesions. Only a few cases of frequent hemorrhaging of peptic ulcers associated with WG have been reported. In our case, a gastric biopsy showed mononuclear cell infiltration in the submucosal area, without granulomas or vasculitis. An endoscopic maneuver, as well as administration of immunosuppressive agents, combined with an H2 receptor antagonist and proton pump inhibitor successfully eliminated the gastrointestinal bleeding. In this case, proof that the gastrointestinal involvement was pathologically related to WG could not be demonstrated because neither granulomas nor vasculitis were observed in the insufficient biopsy specimen of the stomach. It is also possible that the uremic state and cytotoxic agents worsened the gastrointestinal involvement. However, immunosuppressive therapy combined with routine antiulcer treatment was very effective in repairing the ulcerative lesions. The gastrointestinal involvement was considered a possible complication of the WG.
我们治疗了一名55岁的男性韦格纳肉芽肿(WG)患者,该患者伴有多个溃疡性病变导致的频繁胃出血。仅有少数关于与WG相关的消化性溃疡频繁出血的病例报道。在我们的病例中,胃活检显示黏膜下区域有单核细胞浸润,无肉芽肿或血管炎。内镜操作以及免疫抑制剂的使用,联合H2受体拮抗剂和质子泵抑制剂成功消除了胃肠道出血。在该病例中,由于在不足的胃活检标本中未观察到肉芽肿或血管炎,因此无法证明胃肠道受累与WG在病理上相关。尿毒症状态和细胞毒性药物也有可能使胃肠道受累情况恶化。然而,免疫抑制治疗联合常规抗溃疡治疗在修复溃疡性病变方面非常有效。胃肠道受累被认为是WG的一种可能并发症。