Magnetic resonance imaging of pyomyositis in 43 cases
Introduction
Pyomyositis is a primary infection of skeletal muscles, endemic in tropical climates, but rare elsewhere. It presents as an enlarging soft tissue mass associated with pain. Usually, there are no skin changes and the diagnosis may be difficult clinically, because pyomyositis arises deep in the muscle [1], [2], [3]. MRI has become the technique of choice for diagnosis of soft-tissue masses [2]. However, although specific tissue diagnosis is often impossible, characteristic findings have been described for muscle abscess [1], [3], [4], [5]. Accurate assessment of the location and the extent of soft tissue infection is essential for proper treatment, which may include antibiotics, drainage and surgical debridement. Several case reports and a few series have analyzed the role of magnetic resonance imaging (MRI) in detecting soft tissue infection and fluid collections [1], [3], [4], [6]. We reviewed the MRI in 43 patients with proven pyomyositis to identify those characteristics that might be useful in diagnosis.
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Material and methods
We retrospectively reviewed the MRI and clinical findings in 43 patients (30 men and 13 women ranging in age from 14 to 86 years) with proven muscle infection over a period of 4 years. Image analysis was performed by two radiologists and any discrepancies were resolved by consensus. The MRI was performed because of clinical suspicion of soft-tissue infection (n=27), soft-tissue tumour (n=12), thrombophlebitis (n=3) or lymphedema (n=1). A review of patient charts showed that the predisposing
Results
The final diagnoses and the location of musculoskeletal infections are summarized in Table 1. The most common cultured organism was Staphylococcus aureus (62.8%) and Mycobacterium tuberculosis (18.6%). The frequency of muscle, fascial planes, subcutaneous tissue, joints and bone marrow involvement is summarized in Table 2. Isolated muscle infection was found in 10 (23.2%) cases, three resulting from M. tuberculosis. The majority of patients (76.8%) had involvement of multiple structures:
Discussion
Pyomyositis is a primary infection of the skeletal muscle. It is endemic in the tropics and, although usually considered rare in temperate regions, it is becoming more common. Outside the tropics, pyogenic myositis tends to occur more frequently in patients with concurrent diseases such as diabetes, human immunodeficiency virus infection, connective tissue disorder or in patients who are immunodeficient for other reasons [1], [3], [7]. S. aureus is the organism responsible in 90% of cases and
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2018, Orthopaedics and Traumatology: Surgery and ResearchCitation Excerpt :While enhanced CT was used in five cases to confirm the diagnosis. Recently, if there is any doubt in diagnosis we recommended as other authors the enhanced MRI which is considered the most accurate up to date diagnostic tool for confirming the diagnosis of PM which was used in ten patients in our series [12,13,15,17]. Staphylococcus aureus is the most common causative agent reported in the literature [2–16].