Abstract
Pyogenic myositis (pyomyositis) represents a bacterial infection of muscle, usually caused by Staphylococcus aureus that is endemic in tropical regions. Pyomyositis commonly affects patients who are immunocompromised or who have underlying chronic disorders. Lower extremity localization of infection is typical. The most common pattern of disease, however, appears to be a solitary abscess in the quadriceps musculature. Delay in accurate diagnosis is frequent and clinical deterioration can be precipitous. In view of the high associated morbidity, early imaging to detect, localize, and define disease extent is important. Magnetic resonance imaging (MRI) plays a key role in the definitive diagnosis of pyomyositis. This article provides a pictorial illustration of the spectrum of MRI findings associated with pyogenic myositis.
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Pyomyositis: the disease
Pyogenic myositis (pyomyositis), a serious infection of skeletal muscle, is typically seen in tropical regions (tropical pyomyositis) [1] where it affects mainly children and young adults following penetrating trauma. Recently, pyomyositis has been reported in intravenous drug abusers, diabetics, and malnourished and immunodeficient patients, including patients with the acquired immunodeficiency syndrome (AIDS) [1, 2]. Because of an increasing number of immunocompromised and substance abuse patients, however, the risk of this soft tissue infection is likely to increase.
Local muscle trauma may increase susceptibility of skeletal muscle to infection [3, 4]. A variety of pathogens can cause pyogenic myositis, with Staphylococcus aureus accounting for 90% of the cases [3, 4]. Patients with pyomyositis present with symptoms of fever, pain, and swelling of affected muscle(s) [2, 4, 5]. Because of atypical symptoms and signs, the infection is often initially misdiagnosed as muscle strain, thrombophlebitis, osteomyelitis and septic arthritis, hematoma, lymphedema, and neoplasm [2, 5]. Not infrequently, nonspecific clinical presentation results in delayed diagnosis of muscle infection.
Given that pyogenic myositis can result in serious disability, early recognition of pathology is critical to implementing aggressive treatment, often allowing calamitous complications as systemic toxicity or death to be avoided. Imaging plays a central role in early and accurate diagnosis. Radiography has a limited role in imaging muscle infection because usually, it does not demonstrate soft tissue changes directly. Rather, radiography reveals indirect signs of infectious involvement, such as an increase in soft tissue volume, or deformation or obliteration of fat planes [1, 6]. Radionuclide studies with indium 111 and gallium 67 isotopes are sensitive for the diagnosis of pyomyositis [1, 7–9]. The limitations of scintigraphy, however, include low specificity, increased examination time, inability to provide anatomic detail, and radiation exposure. For these reasons, scintigraphy generally has been relegated to a supplemental role in those patients with clinical suspicion of additional nearby or distant abscesses or patients who have indeterminate computed tomography (CT) or MRI findings [10].
Sonography is most useful in the evaluation of superficial abscesses, as deep intramuscular fluid collections (i.e., in the pelvic and lumbar regions) usually require cross-sectional imaging studies [11]. For example, in one study of 12 children with pyomyositis, sonography revealed infectious changes in all cases with involvement of the extremities and identified the infectious condition in only 25% of cases with involvement of the pelvis [12]. Further, sonography is sensitive in the detection of clinically occult fluid collections and can be used to guide biopsy or aspiration [4, 12, 13]. Not infrequently, however, aspiration is required to differentiate an abscess from other types of fluid collections, such as hematoma, seroma, and cystic or necrotic tumors [11]. In the absence of an abscess, the sonographic diagnosis of pyomyositis can be difficult as altered echogenicity in the affected muscle(s) can be subtle [12].
On CT images, the infected muscle group appears enlarged and shows abnormal decreased attenuation [14–16]. CT can document the presence of an intramuscular accumulation of fluid or gas and is particularly useful in guiding therapeutic drainage procedures, especially when deep abscesses are detected [14, 17]. MRI has emerged as the imaging method of choice in assessing a large number of soft tissue abnormalities [4, 6, 7]. MRI generally is preferred over CT because it is highly sensitive, although not highly specific, for early detection of the infectious process (before the development of a frank abscess) and precise delineation of the inflamed muscle(s) [5, 10, 13–16, 18–21]. MRI can provide detailed information regarding the localization and regional extent of infection and the presence or absence of surgical lesions, such as abscesses [4, 22–24].
In this review, we present the MRI findings seen with both the early and late stages of pyogenic myositis at various sites in patients who had sustained local muscle trauma.
Pathophysiology of muscle infection
Although virtually every infectious agent has the potential to cause pyomyositis, little is known about the early pathophysiology or the pathogenetic mechanisms involved in the various forms of the disease. Skeletal muscle is resistant to bacterial infection [1, 5]. It is well documented that under normal circumstances, there is sequestration of iron, a nutritional requirement of proliferating bacteria, by myoglobin, which prevents establishment of infection. Once damaged, skeletal muscle is susceptible to hematogenous invasion by bacteria. Pyomyositis is regarded as a result of compromised muscle resistance to infection via transient bacteremia. Included among the multiple factors associated with muscle damage are trauma, bacterial, parasitic, viral and spirochetal infection, nutritional deficiencies, and underlying disease [3–5]. Indeed, local muscle trauma results in muscle infection in almost 40% of cases [3, 25]. Large muscle groups in the lower extremity, especially in the thigh and buttocks, are affected more frequently than muscles in the upper extremity or trunk [1, 5] (Fig. 1). Although involvement of a single muscle group is typical, in a large series of patients with pyomyositis, multiple lesions were found in 43% of patients [26].
In patients with pyomyositis, versatility of predisposing factors or pathogenetic mechanisms has led clinicians to conclude that the etiology of muscle infection is likely multifactorial. Because different management approaches are applied to each stage of infection, early diagnosis is critical for optimizing clinical treatment of these patients. MRI is very sensitive for detecting inflammatory changes within muscle and provides useful information about the severity of infection [4, 13, 22]. In addition, the lack of ionizing radiation in MRI is particularly advantageous in the typically younger population evaluated for pyogenic myositis.
MRI technique
Infection affecting skeletal muscle can cause alteration in muscle size, shape, or signal intensity. The characteristic MRI findings of pyogenic myositis include muscle swelling and enlargement, with or without intramuscular abscesses [1, 2]. Several MRI protocols can be implemented for imaging inflammatory changes in muscle. At our institution, MRI is performed using a 1.5-T system (Signa, GE Healthcare). Coronal and axial T1-weighted spin echo sequences [TR/TE, 500–700/9–16] and T2-weighted fast spin-echo (4,000–5,800/58–110) with fat suppression are performed in each case. Imaging in the sagittal plane is often done. An alternative to the fat-suppressed T2-weighted sequence is a STIR sequence. T1-weighted MR sequences after intravenous administration of gadolinium-based contrast material are useful in determining whether muscle is viable or necrotic [13]. In patients with diffuse pain and a suspected lesion, the use of a large field of view to include both sides of the body allows assessment of muscle symmetry and may prove helpful in the detection of subtle signal intensity changes.
Clinical and MRI features
Regardless of its etiology, pyogenic myositis comprises three clinical stages [3, 5]. The first, invasive stage occurs at the time the organism enters the muscle and is characterized by pain and swelling of the involved muscle group with minimal changes in the overlying skin and low-grade fever. The second, suppurative or purulent stage relates to the formation of deep collection of pus in the muscle and is characterized by intense pain, fever, and marked edema of affected muscle. The third, late stage is characterized by the presence of fluctuant abscess(es) with necrosis of the affected muscle (myonecrosis), pain, high fever, and septic shock. Patients rarely present in the early stage of infection, while most patients present at the purulent stage. Gradual resolution of symptoms and recovery is the rule when diagnosis is not delayed. In those cases with fluctuation and systemic manifestations, especially patients with AIDS, the infection may lead to fatal outcome [3].
In pyogenic myositis, a muscle is replaced by fluid and inflammatory cells [3]. Consequently, in the early stage of infection, the affected muscle is enlarged and shows preserved intermediate to slightly increased signal intensity compared with normal muscle on T1-weighted images and abnormal high signal intensity on T2-weighted and STIR images (Fig. 2). With progression of the inflammatory process, MR images reveal single or multiple intramuscular abscesses characterized by a peripheral rim of increased signal intensity, representing blood products on T1-weighted images and a central region, representing fluid, of intense signal on T2-weighted and STIR images (Fig. 3a–c). Pus within the abscess can be hypointense, isointense, or hyperintense on T1-weighted images depending on the proteinaceous content of the fluid collection (Figs. 3d, 4 and 5). The rim surrounding the abscess is hypointense on T2-weighted images and enhances after intravenous administration of gadolinium-based contrast material, whereas necrotic tissue and purulent material show no enhancement [1, 2, 4, 13, 22, 25] (Fig. 6). Abscesses are of variable size and extent, and typically form deep in the infected muscle (Figs. 7, 8 and 9). On rare occasions, an abscess may be mistaken for myonecrosis because both abnormalities are characterized by contrast enhancement at the periphery of lesion; abscess generally may be differentiated on T2-weighted images by a presence of central high signal intensity and a mass effect [2]. In patients with pyogenic myositis, subcutaneous edema and unorganized phlegmonous collections may be seen in soft tissue adjacent to areas of active muscle inflammation. Osteomyelitis and septic arthritis can be additional complications of spread of muscle infection to surrounding structures [1].
Treatment
Reducing morbidity and mortality rests on early diagnosis and prompt treatment. Management includes aggressive antibiotic treatment, needle aspiration and/or abscess drainage and surgical debridement [3]. Identification of the infectious microorganism in the pus, which may be sterile in 15–30% of cases, allows administration of the appropriate antimicrobial agent [10]. Penicillin is the drug of choice for infections caused by penicillin susceptible staphylococcus, while effective alternatives are also used for reasons related to breadth of spectrum. In addition to antistaphylococcal antibiotics, immunocompromised patients and patients with AIDS receive broad-spectrum antibiotics including aminoglycosides and clindamycin [10]. In each case, the duration of treatment is adjusted to the patient’s clinical course.
Conclusion
Pyogenic myositis has been—and will remain—a serious infection of muscle, with corresponding MRI findings that range from muscle swelling, to intramuscular abscess(es), to muscle destruction and necrosis. As expected, early-stage muscle infection has a better prognosis than late-stage infection. Because patients with early stage pyogenic myositis present with nonspecific symptoms and signs, diagnosis is often delayed. MRI plays a pivotal role in timely diagnosis, precise localization, and definition of the extent of muscle infection. Recognition and accurate diagnosis of this life-threatening infection is critical for rapid initiation of treatment and resolution of symptoms.
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Theodorou, S.J., Theodorou, D.J. & Resnick, D. MR imaging findings of pyogenic bacterial myositis (pyomyositis) in patients with local muscle trauma: illustrative cases. Emerg Radiol 14, 89–96 (2007). https://doi.org/10.1007/s10140-007-0593-1
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DOI: https://doi.org/10.1007/s10140-007-0593-1