Corrêa João R, Silva Ana P, Pacheco Maria J, Gonçalves Renato, Estevão Dália
Internal Medicine, Centro Hospitalar e Universitário Cova da Beira, Covilhã, PRT.
Rheumatology, Centro Hospitalar e Universitário Cova da Beira, Covilhã, PRT.
Cureus. 2024 Sep 29;16(9):e70446. doi: 10.7759/cureus.70446. eCollection 2024 Sep.
Primary pyomyositis, also known as tropical pyomyositis, is a primary bacterial infection of skeletal muscle following hematogenous infections. It is primarily caused by or Group A and predominantly affects children and young adults. Although rarely observed in temperate climates, its prevalence appears to be increasing. Here, we present the case of a 36-year-old male patient who manifested with persistent fever and inflammatory signs in multiple skeletal muscle locations following acute pharyngitis, further complicated by toxic shock syndrome within 48 h of admission. The blood cultures were positive for and ultrasound evaluation demonstrated muscle tissue heterogeneity, associated with areas of liquid collection and subcutaneous edema, in the right pectoral muscles and bilaterally in the fibularis longus and extensor digitorum longus muscles, confirming the diagnosis of primary pyomyositis. After treatment with a prolonged course of antibiotics, the patient showed substantial clinical improvement and was completely asymptomatic at 6-month follow-up. This case illustrates the possible risks associated with primary pyomyositis and the importance of its early recognition and treatment, regardless of geographic location.
原发性脓性肌炎,也称为热带脓性肌炎,是一种血源性感染后发生的骨骼肌原发性细菌感染。它主要由金黄色葡萄球菌或A组链球菌引起,主要影响儿童和年轻人。虽然在温带气候中很少见,但其发病率似乎在上升。在此,我们报告一例36岁男性患者病例,该患者在急性咽炎后出现多个骨骼肌部位持续发热和炎症体征,并在入院后48小时内并发中毒性休克综合征。血培养结果显示金黄色葡萄球菌阳性,超声评估显示右侧胸肌以及双侧腓骨长肌和趾长伸肌的肌肉组织不均匀,伴有液体积聚和皮下水肿区域,确诊为原发性脓性肌炎。经过长时间抗生素治疗后,患者临床症状有显著改善,在6个月随访时完全无症状。该病例说明了原发性脓性肌炎可能存在的风险以及早期识别和治疗的重要性,无论地理位置如何。