Mihanovic Ivan, Beck Relja, Petric Marin, Raskovic Natasa Males, Huljev Ana Dunatov, Perkovic Dijana, Ivelja Mirela Pavicic
MD, Infectious Diseases Department, University Hospital of Split, Soltanska 1, HR-21000 Split, Croatia.
MD, PhD, Department for Bacteriology and Parasitology, Croatian Veterinary Institute, HR-10000 Zagreb, Croatia.
Germs. 2024 Sep 30;14(3):287-293. doi: 10.18683/germs.2024.1439. eCollection 2024 Sep.
Alveolar echinococcosis is one of the most pathogenic zoonoses caused by the larval forms of . 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.
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.
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.
肺泡型棘球蚴病是由棘球绦虫幼虫引起的最具致病性的人畜共患病之一。该病在中欧为地方病,但在2001年至2018年期间,8个欧洲国家报告了首例肺泡型棘球蚴病病例。这些数字证明了该感染前所未有的传播。
我们报告了克罗地亚南部首例肺泡型棘球蚴病病例,该病例偶然发现于一名70岁免疫功能低下的男性患者。他因肉眼血尿和肾功能不全入院。对肾脏损害的诊断评估发现肝脏有大片浸润,其影像学表现怀疑为癌症。然而,肝脏活检的组织病理学和分子分析证实为肺泡型棘球蚴病。由于病变沿主要肝血管扩展,无法切除。因此,开始使用阿苯达唑进行保守治疗,并调整了现有的免疫抑制治疗。阿苯达唑治疗11个月后的对照影像学检查显示病变有所消退。
尚不清楚该病例是输入性还是本地发生的,但欧洲肺泡型棘球蚴病的发病率显然在上升。由于该病罕见且具有恶性性质,常常被误诊或诊断较晚,此时无法进行根治性手术治疗。临床医生应意识到这种新发寄生虫病,尤其是在免疫功能低下的患者中,因为诊断的每一次延误都会严重影响治疗效果。非常需要更好的治疗选择以及针对这些患者免疫抑制治疗调整的标准化指南。