Imaging of extraspinal musculoskeletal tuberculosis
Introduction
Tuberculosis (TB) remains a common illness among immigrants to the industrialized countries from underdeveloped regions. The prevalence of TB is also high among patients with AIDS, and often represents the first manifestation of HIV infection [1], [2]. Extrapulmonary manifestations are estimated to occur in approximately 20% of patients with TB, most often presenting as lymphadenopathy and genitourinary disease [3]. Extraspinal musculoskeletal TB is among the least common manifestations of TB with a relative frequency of about 1–2% [4]. The reported frequency of peripheral arthritis is 60%, of osteomyelitis 48%, and of tenosynovitis and bursitis 2% [5], [6], [7], [8]. Previous or current pulmonary TB is detected in only about one half of these patients.
A non-specific, often indolent clinical presentation together with a low prevalence and low index of suspicion may result in delayed diagnosis of extraspinal musculoskeletal TB. However, prompt diagnosis and treatment of this curable disease remain critical to minimize pain, maintain joint function, and prevent joint deformity and serious bone destruction [9]. Diagnosis of extraspinal musculoskeletal TB is not possible solely based on clinical or imaging findings. However, in the appropriate clinical setting, radiological assessment may guide diagnostic work-up and may result in earlier and adequate treatment. Histopathological examinations and culture identification are among the most accurate methods for definite diagnosis.
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Pathogenesis
Mycobacterium tuberculosis is the main causative organism of extraspinal musculoskeletal TB and only a few cases are attributable to Mycobacterium bovis. Atypical mycobacteria, such as Mycobacterium kansasii, Mycobacterium marinum, Mycobacterium scrofulaceum, and Mycobacterium avium complex account for approximately 1–4% of cases of tuberculosis [10].
A musculoskeletal TB lesion mainly results from hematogenous dissemination or lymphogenous spread from a primarily or reactivated infected focus
Tuberculous arthritis
As in most infectious joint diseases, TB arthritis is usually monoarticular. In approximately 10% of patients, however, multiple joints may be involved [18]. In musculoskeletal TB, involvement of the synovial joints is the second most frequent location following spinal TB [17]. Most commonly involved joints are the hip and knee, followed by, in order of frequency, the sacroiliac joint, shoulder, elbow, and ankle in order of frequency (Fig. 1, Fig. 2, Fig. 3, Fig. 4, Fig. 5). However, according
Extra-axial tuberculous osteomyelitis
TB osteomyelitis is less common than TB arthritis. Previously, TB osteomyelitis was more often multifocal and disseminated as a result of hematogenous spread from a primary focus mostly in the lungs, or lymphatic system [26]. However, recent reports indicate that solitary lesions are now more commonly seen [17]. Although a pulmonary focus is often presumed, intercurrent active pulmonary TB is seen in a minority of the patients. TB osteomyelitis occurs most commonly in bones of the extremities,
Tuberculous tenosynovitis and bursitis
Primary TB tenosynovitis is considered an extremely rare condition, most commonly involving the flexor tendon sheaths of the dominant hand [6]. TB tenosynovitis may result from hematogenous spread or may be a secondary finding resulting from periarticular extension of TB arthritis (Fig. 5, Fig. 7). Either tendon, synovium, or both may be infiltrated and thickened. Tubercle formation may result in caseation necrosis and secondary effusion within the tendon sheath. Disease progression may lead to
Conclusion
A wide range of imaging findings in extraspinal musculoskeletal TB may be seen, according to whether the infection is confined to joints, skeleton, muscles, tendon sheaths or synovial bursae and whether there is secondary extension to the neighboring tissues. Extraspinal musculoskeletal TB, however, produces no pathognomonic imaging signs, and in advanced stages mimics other disease processes. Although the diagnosis depends largely on the clinical context, ultrasound, CT, and especially, MRI
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