Stavropoulou E, Coste A T, Beigelman-Aubry C, Letovanec I, Spertini O, Lovis A, Krueger T, Burger R, Bochud P Y, Lamoth F
Infectious Diseases Service, Department of Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Institute of Microbiology, Department of Laboratories, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
BMC Infect Dis. 2020 Jul 22;20(1):527. doi: 10.1186/s12879-020-05218-w.
Conidiobolus spp. (mainly C. coronatus) are the causal agents of rhino-facial conidiobolomycosis, a limited soft tissue infection, which is essentially observed in immunocompetent individuals from tropical areas. Rare cases of invasive conidiobolomycosis due to C. coronatus or other species (C.incongruus, C.lamprauges) have been reported in immunocompromised patients. We report here the first case of invasive pulmonary fungal infection due to Conidiobolus pachyzygosporus in a Swiss patient with onco-haematologic malignancy.
A 71 year-old female was admitted in a Swiss hospital for induction chemotherapy of acute myeloid leukemia. A chest CT performed during the neutropenic phase identified three well-circumscribed lung lesions consistent with invasive fungal infection, along with a positive 1,3-beta-d-glucan assay in serum. A transbronchial biopsy of the lung lesions revealed large occasionally septate hyphae. A Conidiobolus spp. was detected by direct 18S rDNA in the tissue biopsy and subsequently identified at species level as C. pachyzygosporus by 28S rDNA sequencing. The infection was cured after isavuconazole therapy, recovery of the immune system and surgical resection of lung lesions.
This is the first description of C. pachyzygosporus as human pathogen and second case report of invasive conidiobolomycosis from a European country.
耳霉属(主要是冠耳霉)是鼻面部耳霉病的病原体,这是一种局限性软组织感染,主要见于热带地区免疫功能正常的个体。免疫功能低下患者中曾有罕见的因冠耳霉或其他物种(不协调耳霉、亮耳霉)引起的侵袭性耳霉病病例报道。我们在此报告瑞士一名患有血液系统恶性肿瘤的患者首例因厚壁耳霉引起的侵袭性肺部真菌感染病例。
一名71岁女性因急性髓系白血病诱导化疗入住瑞士一家医院。在中性粒细胞减少期进行的胸部CT检查发现三个边界清晰的肺部病变,与侵袭性真菌感染相符,同时血清1,3-β-D-葡聚糖检测呈阳性。对肺部病变进行的经支气管活检显示有大型、偶尔有隔膜的菌丝。通过组织活检中的直接18S rDNA检测到耳霉属,随后通过28S rDNA测序在种水平鉴定为厚壁耳霉。在接受艾沙康唑治疗、免疫系统恢复以及对肺部病变进行手术切除后,感染得以治愈。
这是首次将厚壁耳霉描述为人类病原体,也是来自欧洲国家的侵袭性耳霉病的第二例病例报告。