Tezuka Junko, Abe Noriyuki, Tanabe Hiroshi
Department of Dermatology, Tenri Hospital, Tenri 632-8552, Japan.
Department of Laboratory Medicine, Tenri Hospital, Tenri 632-8552, Japan.
Microorganisms. 2025 Mar 17;13(3):671. doi: 10.3390/microorganisms13030671.
Actinomycosis is a chronic suppurative granulomatous disease caused by spp. Although cutaneous actinomycosis is rare, dermatologists must consider it due to its potential coexistence with other pathogens, often as part of polymicrobial infections. We present a rare case of primary axillary cutaneous actinomycosis in a young woman, likely triggered by cosmetic axillary hair removal and home shaving practices. Histological examination revealed characteristics of actinomycosis, including sulfur granules and Gram-positive filamentous structures. Bacterial cultures failed to isolate , but identified , (MRSA), and , suggesting a polymicrobial infection contributing to the inflammatory response. Molecular analysis of DNA extracted from formalin-fixed paraffin-embedded (FFPE) tissue yielded a 675 bp PCR product using -specific primers. BLAST analysis confirmed the species as , establishing the diagnosis of actinomycosis. However, a 1000 bp PCR product obtained using universal 16S rDNA primers could not be sequenced successfully, likely due to the presence of multiple bacterial species. Notably, was detected only through molecular methods, while bacterial cultures identified the aforementioned bacteria. This discrepancy between FFPE-PCR results and bacterial culture findings demonstrates a key challenge in the microbiological diagnosis of polymicrobial infections. This case highlights the importance of integrating histopathological, microbiological, and molecular techniques for accurate pathogen identification in polymicrobial infections. The failure to detect in bacterial cultures, despite its presence in FFPE-PCR, suggests that conventional culture methods alone may be insufficient for diagnosing such infections. Extended culture durations, selective anaerobic culture techniques, and molecular diagnostic methods are essential for a comprehensive evaluation. Recognizing as more than a contaminant is important for timely diagnosis and effective treatment. Increased awareness of its potential involvement in polymicrobial infection should improve clinical outcomes.
放线菌病是一种由放线菌属引起的慢性化脓性肉芽肿性疾病。虽然皮肤放线菌病很少见,但皮肤科医生必须考虑到它,因为它可能与其他病原体共存,通常是作为多微生物感染的一部分。我们报告了一例年轻女性原发性腋窝皮肤放线菌病的罕见病例,可能是由腋窝美容脱毛和家庭剃须行为引发的。组织学检查显示放线菌病的特征,包括硫颗粒和革兰氏阳性丝状结构。细菌培养未能分离出放线菌,但鉴定出了金黄色葡萄球菌(MRSA)、表皮葡萄球菌和痤疮丙酸杆菌,提示多微生物感染导致了炎症反应。使用放线菌特异性引物对从福尔马林固定石蜡包埋(FFPE)组织中提取的DNA进行分子分析,得到了一个675 bp的PCR产物。BLAST分析证实该菌种为放线菌,从而确立了放线菌病的诊断。然而,使用通用16S rDNA引物获得的1000 bp PCR产物未能成功测序,可能是由于存在多种细菌。值得注意的是,放线菌仅通过分子方法检测到,而细菌培养鉴定出了上述细菌。FFPE-PCR结果与细菌培养结果之间的这种差异表明了多微生物感染微生物学诊断中的一个关键挑战。该病例强调了整合组织病理学、微生物学和分子技术以准确鉴定多微生物感染病原体的重要性。尽管FFPE-PCR中存在放线菌,但在细菌培养中未能检测到,这表明仅传统培养方法可能不足以诊断此类感染。延长培养时间、选择性厌氧培养技术和分子诊断方法对于全面评估至关重要。认识到放线菌不仅仅是一种污染物对于及时诊断和有效治疗很重要。提高对其可能参与多微生物感染的认识应能改善临床结果。