A Canadian children's hospital's experience with cystic echinococcosis over 30 years: A case series.

Q3 Medicine JAMMI Pub Date : 2024-01-16 eCollection Date: 2024-01-01 DOI:10.3138/jammi-2022-0041
Kescha Kazmi, Carsten Krueger, Waison Wong, Reto M Baertschiger, Charles Hui, Anita Nagy, Oscar M Navarro, Fathima Razik, Kevin L Schwartz, Andrea K Boggild, Shaun K Morris
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Abstract

Background: Cystic echinococcosis (CE) or hydatid disease caused by the cestode Echinococcus granulosus sensu lato is an uncommon infection in Canada especially among children. There are limited reports describing the clinical presentation and management in Canadian children.

Methods: The medical records of all children diagnosed with CE at a quaternary paediatric centre in Ontario between January 1988 and August 2021 were retrospectively reviewed. The clinical course, management, and outcomes of each case were summarized.

Results: We report two paediatric cases of cystic echinococcosis (CE) in detail and review four additional cases seen at our institution over 33.5 years. The first case was a previously healthy 12-year-old boy with pulmonary CE resulting in unilateral lung collapse and mediastinal shift, who was presumedly infected while living in the Middle East. The second case was a previously healthy 3-year-old girl with pulmonary CE acquired locally in southern Ontario. Four other cases of CE with hepatic involvement (median age 12.5 years) were identified during the study period. Five out of six patients received both surgical and medical therapy.

Conclusion: CE is a rare but serious disease seen in southern Canada that has historically been associated with travel or migration. Due to changes in urban wildlife landscapes and increased global migration, CE may become more prevalent in Canadian children. We describe the first locally acquired case in rural southern Ontario diagnosed at our centre. Prompt recognition of this infection in children by health care providers is important to prevent morbidity and mortality.

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加拿大一家儿童医院 30 多年来治疗囊性棘球蚴病的经验:病例系列。
背景:囊性棘球蚴病(CE)或由普通棘球蚴引起的包虫病在加拿大并不常见,尤其是在儿童中。有关加拿大儿童的临床表现和治疗方法的报告很有限:方法:回顾性审查了 1988 年 1 月至 2021 年 8 月期间在安大略省一家四级儿科中心确诊为棘球蚴病的所有儿童的病历。结果:我们报告了两例儿童囊肿病例:我们详细报告了两例囊性棘球蚴病(CE)儿科病例,并回顾了 33.5 年来在我院就诊的另外四例病例。第一个病例是一名先前健康的 12 岁男孩,肺部棘球蚴病导致单侧肺塌陷和纵隔移位,推测他是在中东生活时感染的。第二个病例是一名原本健康的 3 岁女孩,在安大略省南部当地感染了肺动脉高压。研究期间还发现了另外四例肝脏受累的 CE 病例(中位年龄为 12.5 岁)。六名患者中有五名同时接受了手术和药物治疗:CE是加拿大南部一种罕见但严重的疾病,历来与旅行或迁徙有关。由于城市野生动物景观的变化和全球移民的增加,CE 可能会在加拿大儿童中更加流行。我们描述了本中心在安大略省南部农村地区诊断出的首例本地感染病例。医护人员及时发现儿童感染这种疾病对于预防发病和死亡非常重要。
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来源期刊
JAMMI
JAMMI Medicine-Infectious Diseases
CiteScore
3.80
自引率
0.00%
发文量
48
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