Ohwada S, Yanagisawa A, Joshita T, Yanagisawa T, Iino Y, Izumi M, Inoue T, Komiya J, Morishita Y
Second Department of Surgery, Gunma University School of Medicine, Maebashi, Japan.
Hepatogastroenterology. 1997 Jul-Aug;44(16):1090-4.
A 52-year-old man suffering neither from allergies or asthma, with necrotizing granulomatous vasculitis (allergic granulomatosis) of the transverse colon and gallbladder is presented. During an emergency laparotomy, segmental necrosis of the mesenteric side of the mid-transverse colon, and a bulky enlarged gallbladder were found. The affected colon was resected and cholecystectomy was performed. Histological findings included necrotizing granulomatous vasculitis of the small- and medium-sized muscular arteries and adjacent veins with tissue infiltration by eosinophils and extravascular eosinophilic granulomas. These histological features were compatible with allergic granulomatous angitis described by Churg and Strauss (CSS). The patient had neither asthma nor involvement of two or more extra-pulmonary organs which is a key clinical criteria of CSS and fulfilled the criteria of eosinophilia alone. Although pulmonary vasculitis was not confirmed in this patient, the histological diagnosis of this patient was definitive CSS. Localised PAN with allergic granulomatosis or an isolated or limited form of CSS based on these clinical features may be an alternative entity.
本文报告了一名52岁男性,既无过敏史也无哮喘病史,患有横结肠和胆囊的坏死性肉芽肿性血管炎(过敏性肉芽肿病)。在急诊剖腹手术中,发现横结肠中部肠系膜侧节段性坏死以及胆囊肿大。切除了受累的结肠并进行了胆囊切除术。组织学检查结果包括中小肌性动脉及相邻静脉的坏死性肉芽肿性血管炎,伴有嗜酸性粒细胞组织浸润和血管外嗜酸性肉芽肿。这些组织学特征与Churg和Strauss描述的过敏性肉芽肿性血管炎(CSS)相符。该患者既无哮喘,也未累及两个或更多肺外器官,而这是CSS的关键临床标准,仅符合嗜酸性粒细胞增多的标准。尽管该患者未证实有肺部血管炎,但该患者的组织学诊断为确诊的CSS。基于这些临床特征,伴有过敏性肉芽肿病的局限性结节性多动脉炎或CSS的孤立或局限性形式可能是一种替代实体。