D'Alessandro Antonio, Rausch Robert L
Department of Tropical Medicine, School of Public Health and Tropical Medicine SL-29, Tulane University, 1440 Canal Street, Suite 2210, New Orleans, Louisiana 70112-2824, USA.
Clin Microbiol Rev. 2008 Apr;21(2):380-401, table of contents. doi: 10.1128/CMR.00050-07.
Of the four species of the genus Echinococcus (Cestoda) distinguished by biological and morphological characteristics, two species, E. vogeli and E. oligarthrus, occur widely in the Neotropics. Approximately 200 cases of polycystic echinococcosis (PE) have been recorded from 12 countries in South America. Following early proliferation of E. vogeli in the human host, typically in the liver, the metacestode usually spreads in the peritoneal and pleural cavities, and numerous organs may be invaded. The clinical characteristics of PE in 81 patients with sufficient information are reviewed. Type I disease consists of polycysts in the liver and abdominal cavity (37% of the patients had this characteristic); type II is similar to type I but also includes hepatic insufficiency (26%); type III consists of cysts in liver and chest (14%); type IV consists of cysts only in the mesenteries (16%); and type V consists of cysts calcified in liver and lung (4%). The percentage of patients with polycysts in the liver was 81%, and the percentage of patients with polycysts in the chest was 14%. PE is most ready diagnosed by geographic origin of the patient and by means of ultrasound or computerized tomography scanning showing cysts and calcifications. The highest mortality was for patients with type II disease, due to hepatic failure and its complications. There were five patients who died due to surgical accidents, whereas 35 cases had uncomplicated surgery. Twenty-three patients died of PE, making the total mortality 29% (23 of 78 cases). None of the 13 patients treated only with albendazole, the most efficacious treatment, was completely cured. PE represents a severe medical problem in South America. A reevaluation of the characteristics of the metacestode of E. oligarthrus indicated that it is unicystic. Only three human cases are known (two with infection in the orbit and one with infection in the heart). The metacestode of E. oligarthrus, in contrast with that of E. vogeli, consists of a spherical, fluid-filled vesicle that enlarges concentrically and is not known to undergo exogenous proliferation.
在细粒棘球绦虫属(绦虫纲)的四个物种中,根据生物学和形态学特征区分出的两个物种,即伏氏棘球绦虫和少节棘球绦虫,在新热带地区广泛存在。南美洲12个国家已记录了约200例多囊性棘球蚴病(PE)病例。伏氏棘球绦虫在人体宿主中早期增殖后,通常在肝脏,其幼虫通常在腹膜和胸膜腔扩散,许多器官可能被侵袭。对81例有足够信息的PE患者的临床特征进行了回顾。I型疾病表现为肝脏和腹腔内有多个囊肿(37%的患者有此特征);II型与I型相似,但也包括肝功能不全(26%);III型包括肝脏和胸部有囊肿(14%);IV型仅表现为肠系膜有囊肿(16%);V型表现为肝脏和肺部有钙化囊肿(4%)。肝脏有囊肿的患者比例为81%,胸部有囊肿的患者比例为14%。PE最容易通过患者的地理来源以及超声或计算机断层扫描显示囊肿和钙化来诊断。II型疾病患者的死亡率最高,原因是肝功能衰竭及其并发症。有5例患者死于手术意外,而35例手术无并发症。23例患者死于PE,总死亡率为29%(78例中的23例)。13例仅接受最有效的治疗药物阿苯达唑治疗的患者均未完全治愈。PE在南美洲是一个严重的医学问题。对少节棘球绦虫幼虫特征的重新评估表明它是单囊的。已知仅有3例人类病例(2例眼眶感染,1例心脏感染)。与伏氏棘球绦虫的幼虫不同,少节棘球绦虫的幼虫由一个充满液体的球形囊泡组成,该囊泡同心扩大,且未知会发生外生性增殖。