共查询到20条相似文献,搜索用时 15 毫秒
1.
Angela A. Stanton 《Journal of the American College of Cardiology》2019,73(14):1872-1873
2.
Confusing cortical columns 总被引:2,自引:0,他引:2
Rakic P 《Proceedings of the National Academy of Sciences of the United States of America》2008,105(34):12099-12100
3.
4.
5.
When patients present with chest discomfort, efforts are made to determine whether the symptom is due to myocardial ischemia or something else. Julian, in 1981, suggested that “angina pectoris is a sense of discomfort arising in the myocardium as a result of myocardial ischemia in the absence of infarction.” 1 Copyright © 2009 Wiley Periodicals, Inc. 相似文献
6.
7.
8.
9.
10.
11.
12.
13.
Zhen-Kai Wang Hui Shi Shao-Dong Wang Jiong Liu Wei-Ming Zhu Miao-Fang Yang Chan Liu Heng Lu Fang-Yu Wang 《World journal of gastrointestinal endoscopy》2014,(1)
Behcet's disease(BD) is a rare and life-long disorder characterized by inflammation of blood vessels throughout the body. BD was originally described in 1937 as a syndrome involving oral and genital ulceration in addition to ocular inflammation. Intestinal BD refers to colonic ulcerative lesions documented by objective measures in patients with BD. Many studies have shown that over 40% of BD patients have gastrointestinal complaints. Symptoms include abdominal pain, diarrhea, nausea, anorexia and abdominal distension. Although gastrointestinal symptoms are common, the demonstration of gastrointestinal ulcers is rare. This so-called intestinal BD accounts for approximately 1% of cases. There is no specific test for BD, and the diagnosis is based on clinical criteria. The manifestations of intestinal BD are similar to those of other colitis conditions such as Crohn's disease or intestinal tuberculosis, thus, it is challenging for gastroenterologists to accurately diagnose intestinal BD in patients with ileocolonic ulcers. However, giant ulcers distributed in the esophagus and ileocecal junction with gastrointestinal hemorrhage are rare in intestinal BD. Here, we present a case of untypical intestinal BD. The patient had recurrent aphthous ulceration of the oral mucosa, and esophageal and ileo-colonic ulceration, but no typical extra-intestinal symptoms. During examination, the patient had massive acute lower gastrointestinal bleeding. The patient underwent ileostomy after an emergency right hemicolectomy and partial ileectomy, and was subsequently diagnosed with incomplete-type intestinal BD by pathology. The literature on the evaluation and management of this condition is reviewed. 相似文献
14.
15.
16.
17.
18.
Vecchio P 《Rheumatology (Oxford, England)》2000,39(9):1047
SIR, In support of the recent correspondence regarding the problemwith 相似文献
19.
20.
Wang ZK Shi H Wang SD Liu J Zhu WM Yang MF Liu C Lu H Wang FY 《World journal of gastrointestinal endoscopy》2014,6(1):27-31
Behcet’s disease (BD) is a rare and life-long disorder characterized by inflammation of blood vessels throughout the body. BD was originally described in 1937 as a syndrome involving oral and genital ulceration in addition to ocular inflammation. Intestinal BD refers to colonic ulcerative lesions documented by objective measures in patients with BD. Many studies have shown that over 40% of BD patients have gastrointestinal complaints. Symptoms include abdominal pain, diarrhea, nausea, anorexia and abdominal distension. Although gastrointestinal symptoms are common, the demonstration of gastrointestinal ulcers is rare. This so-called intestinal BD accounts for approximately 1% of cases. There is no specific test for BD, and the diagnosis is based on clinical criteria. The manifestations of intestinal BD are similar to those of other colitis conditions such as Crohn’s disease or intestinal tuberculosis, thus, it is challenging for gastroenterologists to accurately diagnose intestinal BD in patients with ileo-colonic ulcers. However, giant ulcers distributed in the esophagus and ileocecal junction with gastrointestinal hemorrhage are rare in intestinal BD. Here, we present a case of untypical intestinal BD. The patient had recurrent aphthous ulceration of the oral mucosa, and esophageal and ileo-colonic ulceration, but no typical extra-intestinal symptoms. During examination, the patient had massive acute lower gastrointestinal bleeding. The patient underwent ileostomy after an emergency right hemicolectomy and partial ileectomy, and was subsequently diagnosed with incomplete-type intestinal BD by pathology. The literature on the evaluation and management of this condition is reviewed. 相似文献