[胃肠病学]钩端螺旋体病。Universitário加拉加斯医院14例病例研究[1984-1994]。

G.E.N Pub Date : 1995-10-01
P Candia, A Pinto
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引用次数: 0

摘要

对1989年至1994年期间入住加拉加斯大学医院的14例经活抗原微凝集确诊为钩端螺旋体病的病例进行了研究。大多数人都在肠胃科住院。血清学中最常见的是黄疸出血11例。男性占12/2,年龄在31 ~ 40岁之间。最常见的表现形式是:发烧(14),黄疸(10)和肌痛(10),而最相关的体格检查结果是:黄疸(12),发烧(11)和肝肿大(8)。所有患者都有异常的实验室检查,其中转氨酶,胆红素,创造素,CPK,血小板和尿沉渣更频繁地改变。只有一半的患者在入院时被诊断为钩端螺旋体病。我们的结论是,尽管钩端螺旋体病是一种分布在世界各地的传染病,但只有少数病例住院治疗,而且由于临床表现的多样性和缺乏实验室资源,鉴别诊断很困难。这对胃肠病学家来说很重要,因为大多数复杂的病例都表现为黄疸患者。
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[Leptospirosis in Gastroenterology. Study of 14 cases in the Hospital Universitário de Caracas 1984-1994].

14 cases that were admitted to the Hospital Universitario de Caracas, between 1.989 and 1.994, with a definitive diagnosis of Leptospirosis by microaglutination of live antigens were studied. Most of them hospitalized at the gastroenterology service. The serovar most frequently found was icterohemorragiae 11 cases. There was a predominium for the male gender 12/2 and the majority of patients belonged to the range of age between 31 and 40. The most common forms of presentations were: fever (14), jaundice (10) and myalgias (10) while the most relevant findings at physical examination were: jaundice (12), fever (11) and hepatomegaly (8). All patients had abnormal laboratory tests and among these, aminotransferases, bilirrubin, creatinin, CPK, platelets and urinary sediment were more frequently altered. Only half of the patients were diagnosed as Leptospirosis at the moment of admission. We conclude that even though Leptospirosis is an infectious disease distributed worldwide only few cases are hospitalized and differential diagnosis is difficult because of diversity of clinical presentations and lack of laboratory resources. It is important for gastroenterologists because most of complicated cases present as jaundiced patients.

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[Hepatitis C virus]. [Evaluation of methods for the diagnosis of Helicobacter pylori infection]. [Leptospirosis in Gastroenterology. Study of 14 cases in the Hospital Universitário de Caracas 1984-1994]. [Gastrointestinal stromal sarcoma. Report of a case and review of the literature]. [Von Recklinghausen disease and hepatic neurofibromatosis].
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