The first case of alveolar echinococcosis from southern Croatia: progressive course of the disease in an immunocompromised patient.

IF 1.7 Q3 INFECTIOUS DISEASES
GERMS Pub Date : 2024-09-30 eCollection Date: 2024-09-01 DOI:10.18683/germs.2024.1439
Ivan Mihanovic, Relja Beck, Marin Petric, Natasa Males Raskovic, Ana Dunatov Huljev, Dijana Perkovic, Mirela Pavicic Ivelja
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Abstract

Introduction: Alveolar echinococcosis is one of the most pathogenic zoonoses caused by the larval forms of Echinococcus multilocularis. It is endemic in central Europe, but from 2001 to 2018, eight European countries reported their first cases of alveolar echinococcosis. These numbers testify to unprecedented spread of the infection.

Case report: We report the first case of alveolar echinococcosis from southern Croatia that was incidentally found in an immunocompromised 70-year-old male patient. He was admitted to the hospital due to macrohematuria and renal insufficiency. Diagnostic assessment of kidney impairment revealed a large liver infiltration whose radiographic appearance was suspicious of a cancer. Nevertheless, histopathological and molecular analysis of the liver biopsy confirmed alveolar echinococcosis. The lesion was irresectable due to expansion along the major liver vessels. Therefore, conservative treatment with albendazole was started and the existing immunosuppressive therapy was modulated. The control imaging following 11 months of albendazole treatment showed regression of the lesions.

Conclusions: It is not clear whether this case was imported or autochthonous, but it is evident that the incidence of alveolar echinococcosis is rising in Europe. Due to its rareness and malignant nature of the disease, it is often misdiagnosed or diagnosed late when radical surgical treatment is impossible to perform. Clinicians should be aware of this emerging parasitic disease, especially in immunocompromised patients, because every delay in reaching the diagnosis seriously hampers therapeutic efficacy. Better therapeutic options and standardized guidelines on the modulation of immunosuppressive therapy in these patients are highly needed.

来自克罗地亚南部的第一例肺泡包虫病:免疫功能低下患者的病程进展。
肺泡棘球蚴病是由多房棘球蚴幼虫引起的致病性最高的人畜共患病之一。它在中欧流行,但从2001年到2018年,八个欧洲国家报告了第一例肺泡包虫病。这些数字证明了感染的空前蔓延。病例报告:我们报告第一例肺泡包虫病从克罗地亚南部,偶然发现在免疫功能低下的70岁男性患者。他因大量血尿和肾功能不全而入院。肾脏损害的诊断评估显示一个大的肝脏浸润,其影像学表现怀疑是癌症。然而,肝活检的组织病理学和分子分析证实为肺泡包虫病。病变沿肝脏主要血管扩张,无法切除。因此,开始阿苯达唑保守治疗,并调整现有免疫抑制治疗。阿苯达唑治疗11个月后的对照影像学显示病变消退。结论:目前尚不清楚该病例是输入性还是本地性,但很明显,欧洲的肺泡包虫病发病率正在上升。由于该病的罕见性和恶性性质,当根治性手术治疗无法进行时,它经常被误诊或诊断晚。临床医生应该意识到这种新出现的寄生虫病,特别是在免疫功能低下的患者中,因为每次延误诊断都会严重妨碍治疗效果。在这些患者中,迫切需要更好的治疗选择和调节免疫抑制治疗的标准化指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
GERMS
GERMS INFECTIOUS DISEASES-
CiteScore
2.80
自引率
5.00%
发文量
36
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