Beyond the Usual Suspects: A Challenging Case of Disseminated Sporotrichosis Masquerading as Suppurative Lymphadenitis in a Dialysis-Dependent Chronic Kidney Disease Patient With Lupus.

IF 0.8 Q4 INFECTIOUS DISEASES
Case Reports in Infectious Diseases Pub Date : 2026-10-07 eCollection Date: 2026-01-01 DOI:10.1155/crdi/2428389
Natalia Chilinque Zambão da Silva, Jordanna de Paula Mendes Torres, Valéria Regina Soares, Nathalia Antônio de Oliveira Velasco, Violeta Duarte Tortelly Costa, Bruno Carrilho Hollanda
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Abstract

Sporotrichosis, a subcutaneous mycosis, can manifest as severe disseminated disease in immunocompromised hosts. This report describes a challenging case of extracutaneous sporotrichosis in a 28-year-old female with systemic lupus erythematosus (SLE) on immunosuppressive therapy, who also faced significant socioeconomic constraints. The patient initially presented to the emergency department with a painful right inguinal mass. Physical examination revealed a hemorrhagic lesion, and aspiration of the material was performed for culture, which returned negative. She was discharged but returned 2 months later with worsening symptoms and widespread lesions. During this second admission, a detailed history finally revealed contact with cats. The patient was readmitted for an inguinal lymph node biopsy. Histopathological analysis revealed granulomatous lymphadenitis with stellate necrosis, and the diagnosis was ultimately confirmed by culture, identifying Sporothrix schenckii complex. Treatment with itraconazole was initiated but later switched to liposomal amphotericin B due to hepatotoxicity. The patient completed a 1-year course of liposomal amphotericin B with an excellent clinical response. This case highlights the diagnostic complexity of sporotrichosis in patients with SLE, its potential for severe dissemination, and the impact of socioeconomic barriers on timely diagnosis and disease management.

超越通常的怀疑:弥散性孢子菌病伪装成化脓性淋巴结炎的透析依赖慢性肾病伴狼疮患者的一个具有挑战性的案例。
孢子菌病是一种皮下真菌病,可在免疫功能低下的宿主中表现为严重的播散性疾病。本报告描述了一例具有挑战性的皮肤外孢子虫病病例,患者为28岁的系统性红斑狼疮(SLE)患者,接受免疫抑制治疗,同时也面临显著的社会经济限制。患者最初以疼痛的右腹股沟肿块就诊于急诊科。体格检查发现出血性病变,并进行吸出培养,结果为阴性。患者出院,但2个月后复发,症状加重,病变广泛。在第二次入院期间,详细的病史终于揭示了与猫的接触。患者再次入院接受腹股沟淋巴结活检。组织病理学分析显示肉芽肿性淋巴结炎伴星状坏死,最终通过培养确诊为申克孢子丝菌复合体。开始用伊曲康唑治疗,但由于肝毒性,后来改用两性霉素B脂质体。患者完成了为期1年的两性霉素B脂质体治疗,临床反应良好。该病例突出了SLE患者孢子虫病诊断的复杂性,其严重传播的可能性,以及社会经济障碍对及时诊断和疾病管理的影响。
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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