Wang Rong, Xue Yuyuan, Wu Zirong, Wei Mingjing, Wu Nongxin, Guo Jian
Department of Clinical Laboratory Medicine, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Hubei Xiangyang, 441021, China.
Department of Dermatology, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Int J Infect Dis. 2025 Sep 4:108049. doi: 10.1016/j.ijid.2025.108049.
Prototheca, a genus of opportunistic pathogenic microalgae, can cause protothecosis in humans and animals, manifesting as cutaneous lesions or disseminated/systemic infections. This report describes a rare case of Prototheca wickerhamii toe infection in a 78-year-old Chinese male, presenting initially as gouty arthritis. The patient, who worked in fish farming with frequent water exposure, had a history of herpes zoster and hypertension. For three years, he experienced recurrent episodes of erythema, swelling, and pain in the bilateral first metatarsophalangeal joints without identifiable triggers. Symptoms worsened over the past month, leading to hospital admission with suspected gout. Physical examination revealed a 1 cm ulcer on the right foot with a dark red granulation tissue base, extending 4 cm deep. The surrounding skin was erythematous, swollen, exudative, and markedly tender. Laboratory findings showed normal serum uric acid (354 μmol/L) but elevated neutrophil percentage (82.1%). Magnetic resonance imaging (MRI) suggested possible gouty arthritis in the right foot, but no urate crystal deposition was evident. Five days later, re-evaluation revealed significantly elevated interleukin levels (IL-6 >2500 pg/mL, IL-8 157.29 pg/mL), indicating a robust new inflammatory response, with no significant improvement in local symptoms. Concurrently, deep tissue sampling and microbiological investigations (including histopathology, blood agar culture, fluorescent staining, Matrix-Assisted Laser Desorption/Ionization - Time Of Flight (MALDI-TOF) mass spectrometry) and Internal Transcribed Spacer (ITS) sequencing confirmed P. wickerhamii infection. Antifungal therapy was switched to itraconazole, resulting in symptom improvement within five days, and the patient was discharged. This case highlights the variable, masquerading, and potentially severe clinical presentations of P. wickerhamii infection. It underscores the importance of heightened awareness for microbiological screening in cases of suspected "gout" with persistent deep ulcers, particularly in individuals with relevant occupational or environmental exposure histories, especially with normal serum uric acid. Deep tissue sampling for definitive diagnosis is crucial to avoid empiric corticosteroid therapy, which may exacerbate opportunistic infections.
原藻属是一类机会致病性微藻,可导致人类和动物发生原藻病,表现为皮肤病变或播散性/全身性感染。本报告描述了一例罕见的威克汉姆原藻感染78岁中国男性足部的病例,最初表现为痛风性关节炎。该患者从事渔业养殖,经常接触水,有带状疱疹和高血压病史。三年来,他双侧第一跖趾关节反复出现红斑、肿胀和疼痛,无明显诱因。症状在过去一个月加重,因疑似痛风入院。体格检查发现右足有一个1厘米的溃疡,底部为暗红色肉芽组织,深度达4厘米。周围皮肤发红、肿胀、渗出,压痛明显。实验室检查结果显示血清尿酸正常(354 μmol/L),但中性粒细胞百分比升高(82.1%)。磁共振成像(MRI)提示右足可能为痛风性关节炎,但未见尿酸盐结晶沉积。五天后,复查显示白细胞介素水平显著升高(IL-6>2500 pg/mL,IL-8 157.29 pg/mL),表明有强烈的新炎症反应,局部症状无明显改善。同时,深部组织取样和微生物学检查(包括组织病理学、血琼脂培养、荧光染色、基质辅助激光解吸/电离飞行时间(MALDI-TOF)质谱分析)以及内转录间隔区(ITS)测序确诊为威克汉姆原藻感染。抗真菌治疗改为伊曲康唑,五天内症状改善,患者出院。该病例突出了威克汉姆原藻感染的多变、伪装及潜在严重临床表现。强调了对于疑似“痛风”且有持续深部溃疡的病例,尤其是有相关职业或环境暴露史且血清尿酸正常的个体,加强微生物学筛查意识的重要性。进行深部组织取样以明确诊断对于避免经验性使用皮质类固醇治疗至关重要,因为这可能会加重机会性感染。