Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2025 Jun 22;17(6):e86545.
doi: 10.7759/cureus.86545. eCollection 2025 Jun.

An Atypical Case of Infectious Myositis in a Young Woman on Immunosuppressive Therapy

Affiliations
Case Reports

An Atypical Case of Infectious Myositis in a Young Woman on Immunosuppressive Therapy

Jamie Therese Abad et al. Cureus. .

Abstract

Infectious myositis is a rare but serious condition typically caused by bacterial pathogens. In immunocompromised patients, including those on long-term immunosuppressive therapy, clinical signs of myositis can be subtle or delayed. We present the case of a 21-year-old woman with systemic lupus erythematosus (SLE) on immunosuppressive therapy who presented with pain, fever, tachycardia, and swelling of the right lower leg. Initial evaluation revealed no skin defects or rash and normal creatine phosphokinase (CPK) levels. A non-contrast computed tomography (CT) scan of her leg showed some soft tissue changes, but it was only after a week of worsening symptoms that contrast-enhanced CT imaging revealed a multiloculated, large abscess, measuring 23.7 cm in length, in the anterior compartment of the leg. The abscess was drained surgically, and intraoperative cultures grew methicillin-resistant Staphylococcus aureus. The absence of early definitive findings, including a normal CPK level, may have contributed to the delay in diagnosis. This case highlights the diagnostic challenges of infectious myositis in immunosuppressed patients, where early imaging and laboratory findings can be misleading, underscoring the importance of repeated clinical assessment and timely advanced imaging to ensure early detection and appropriate treatment.

Keywords: acute myositis; bacterial myositis; bacterial pyomyositis; infectious myositis; pyomyositis; soft tissue infection.

PubMed Disclaimer

Conflict of interest statement

Human subjects: Informed consent for treatment and open access publication was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Figures

Figure 1
Figure 1. Non-contrast CT of the right lower extremity showing nonspecific soft tissue changes.
Axial (A) and coronal (B) non-contrast CT images of the right lower extremity demonstrate subcutaneous edema and heterogenous hypodensity within the anterior muscle compartment, concerning for muscle atrophy or early inflammation. The red arrow in A highlights the anterior compartment with blurring of fascial planes, suggesting early infectious myositis. No discrete fluid collection is seen. Osseous structures are intact without signs of periostitis, endosteal scalloping, or radiopaque foreign bodies. CT: computed tomography
Figure 2
Figure 2. Contrast-enhanced CT of the right lower extremity showing a large multiloculated abscess.
Contrast-enhanced CT images of the right lower extremity demonstrate a complex, peripherally enhancing, multiloculated fluid collection within the anterior compartment musculature, measuring approximately 5.0 × 3.4 × 23.7 cm and tapering near the right ankle. Subcutaneous fat stranding is present, with no evidence of gas, cortical erosion, or joint effusion. These findings are consistent with infectious myositis complicated by abscess formation. A includes intersecting red dotted lines marking the central area of the fluid collection in the axial view. B shows the full longitudinal extent of the abscess in the coronal plane. CT: computed tomography

Similar articles

References

    1. Purulent infectious myositis (formerly tropical pyomyositis) Habeych ME, Trinh T, Crum-Cianflone NF. J Neurol Sci. 2020;413:116767. - PubMed
    1. Bacterial, fungal, parasitic, and viral myositis. Crum-Cianflone NF. Clin Microbiol Rev. 2008;21:473–494. - PMC - PubMed
    1. Necrotizing myositis: highlighting the hidden depths - case series and review of the literature. Khanna A, Gurusinghe D, Taylor D. ANZ J Surg. 2020;90:130–134. - PubMed
    1. Imaging of musculoskeletal soft tissue infections. Turecki MB, Taljanovic MS, Stubbs AY, Graham AR, Holden DA, Hunter TB, Rogers LF. Skeletal Radiol. 2010;39:957–971. - PubMed
    1. Infective pyomyositis and myositis in children in the era of community-acquired, methicillin-resistant Staphylococcus aureus infection. Pannaraj PS, Hulten KG, Gonzalez BE, Mason EO Jr, Kaplan SL. Clin Infect Dis. 2006;43:953–960. - PubMed

Publication types

LinkOut - more resources