Han Hulin, Kim Hyunsung, Rehman Abdul, Jang Se Min, Paik Seung Sam
Hulin Han, Hyunsung Kim, Abdul Rehman, Se Min Jang, Seung Sam Paik, Department of Pathology, College of Medicine, Hanyang University, Seoul 133-792, South Korea.
World J Clin Cases. 2014 Dec 16;2(12):888-92. doi: 10.12998/wjcc.v2.i12.888.
To determine the incidence of appendiceal Crohn's disease (CD) and to summarize the characteristic histologic features of appendiceal CD.
We reviewed the pathology files of 2179 appendectomy specimens from January 2007 to May 2013. The computer-assisted retrieval search facility was utilized to collect specimens. We selected those cases that were diagnosed as CD or chronic granulomatous inflammation and defined the final diagnosis according to the histologic findings of CD, including transmural lymphocytic inflammation, non-caseating epithelioid granulomas, thickening of the appendiceal wall secondary to hypertrophy of muscularis mucosa, mucosal ulceration with crypt abscesses, mucosal fissures, and fistula formation.
We found 12 cases (7 male and 5 female patients, with an average age of 29.8 years) of appendiceal CD. The incidence of appendiceal CD was 0.55%. The chief complaints were right lower quadrant pain, abdominal pain, lower abdominal pain, and diarrhea. The duration of symptom varied from 2 d to 5 mo. The histologic review revealed appendiceal wall thickening in 11 cases (92%), transmural inflammation in all cases (100%), lymphoid aggregates in all cases (100%), epithelioid granulomas in all cases (100%), mucosal ulceration in 11 cases (92%), crypt abscesses in 5 cases (42%), perforation in 2 cases (17%), muscular hypertrophy in 1 case (8%), neural hyperplasia in 5 cases (42%), and perpendicular serosal fibrosis in 8 cases (67%).
A typical and protracted clinical course, unusual gross features of the appendix and the characteristic histologic features are a clue in the diagnosis of appendiceal CD.
确定阑尾克罗恩病(CD)的发病率,并总结阑尾CD的特征性组织学特征。
我们回顾了2007年1月至2013年5月期间2179例阑尾切除标本的病理档案。利用计算机辅助检索设施收集标本。我们选择那些被诊断为CD或慢性肉芽肿性炎症的病例,并根据CD的组织学表现确定最终诊断,包括透壁淋巴细胞炎症、非干酪样上皮样肉芽肿、黏膜肌层肥大继发的阑尾壁增厚、伴有隐窝脓肿的黏膜溃疡、黏膜裂隙和瘘管形成。
我们发现12例阑尾CD患者(7例男性和5例女性,平均年龄29.8岁)。阑尾CD的发病率为0.55%。主要症状为右下腹疼痛、腹痛、下腹部疼痛和腹泻。症状持续时间从2天到5个月不等。组织学检查显示,11例(92%)阑尾壁增厚,所有病例(100%)均有透壁炎症,所有病例(100%)均有淋巴滤泡聚集,所有病例(100%)均有上皮样肉芽肿,11例(92%)有黏膜溃疡,5例(42%)有隐窝脓肿,2例(17%)有穿孔,1例(8%)有肌层肥大,5例(42%)有神经增生,8例(67%)有垂直性浆膜纤维化。
典型且病程迁延、阑尾不寻常的大体特征以及特征性组织学特征是诊断阑尾CD的线索。