Nguyen John, Singh Pardeep, Gajjar Tapas
Department of Internal Medicine, Baylor Scott & White Medicine Center - Round Rock, Round Rock, Texas.
Proc (Bayl Univ Med Cent). 2023 May 11;36(4):518-520. doi: 10.1080/08998280.2023.2210483. eCollection 2023.
Pyomyositis is an infection of skeletal muscles, commonly affecting deep longitudinal muscles of the lower extremities. Primary pyomyositis is uncommon in the United States. is the most common cause of pyomyositis, but is the most common cause of life-threatening bacterial infection in asplenic patients. Most cases of pyomyositis occur in immunocompromised patients. We describe a 31-year-old man with pyomyositis whose diagnosis and hospital course were complicated by an immunocompromised state from asplenia and an underlying connective tissue disease, Stickler syndrome. Underlying connective tissue diseases such as systemic lupus erythematosus and polymyositis can predispose patients to infection, but susceptibility with Stickler syndrome is less known. While pyomyositis is only seen in up to 0.2% of US hospital admissions, it remains a pertinent differential for patients with asplenia and connective tissue disease.
脓性肌炎是一种骨骼肌感染性疾病,通常累及下肢深部纵行肌肉。原发性脓性肌炎在美国并不常见。[具体细菌名称1]是脓性肌炎最常见的病因,但[具体细菌名称2]是脾切除患者危及生命的细菌感染最常见的病因。大多数脓性肌炎病例发生在免疫功能低下的患者中。我们描述了一名31岁患有脓性肌炎的男性,其诊断和住院过程因脾切除导致的免疫功能低下状态以及潜在的结缔组织病——斯蒂克勒综合征而变得复杂。系统性红斑狼疮和多发性肌炎等潜在的结缔组织病可使患者易发生感染,但斯蒂克勒综合征患者的易感性鲜为人知。虽然脓性肌炎在美国医院入院患者中仅占0.2%,但对于脾切除和结缔组织病患者来说,它仍然是一个相关的鉴别诊断。