Approximately 3months previously, he had consulted an orthopedic surgeon because of low back and leg pain. He had been diagnosed with disc herniation at L4-L5, and had been hospitalized for bed-rest and treatment. While hospitalized, he had received several intravenous injections of sodium salicylate, but no peripheral intravenous catheter had been inserted. About 2months after discharge, he had been referred to our outpatient anesthesiology department because of ongoing leg pain. Two weeks before presentation, he had received his first epidural block using 6ml of 0.8% mepivacaine hydrochloride at the L4-L5 level, injected via the paramedian approach. Two days before presentation, a second epidural block using 5ml of 0.8% mepivacaine hydrochloride had been administered at the same level. The skin had been disinfected with 5% chlorhexidine solution prior to needle insertion on both occasions. His medical history included hypertension and diabetes, for which he was taking antihypertensive and hypoglycemic agents, respectively. He had no history of trauma, shoulder injection, subclavian vein catheterization, or intravenous drug abuse. He did not have any focal dental infection or signs of tooth decay. He was unable to walk, due to increased leg pain. The day prior to admission, he experienced a fever of 39°C.

On examination, he was in moderate respiratory distress and mildly diaphoretic, with a blood pressure of 97/51mmHg, pulse rate of 95 beats/min, respiratory rate of 28 breaths/min, temperature of 39.5°C, and oxygen saturation of 80% on room air. His oxygen saturation improved to 92% with oxygen administration (2l/min by nasal cannula). Examination of the oral cavity and pharynx was normal, and there was no cervical lymphadenopathy. Chest examination was unremarkable except for swelling and severe tenderness over the left SCJ. Lumbar spine examination showed stiffness, with tenderness over the vertebrae. Movement of the lower back and pressure over the lumbar spine caused pain. The straight leg raising test and femoral nerve stretch test were inconclusive bilaterally because of lower back muscle spasm. His lower limb muscle power, knee and ankle reflexes, and sensation were normal. Bladder and bowel function were normal.

Laboratory testing showed the following results: plasma white blood cell count (WBC) 18,490/mm³, platelet count 541,000/mm³, hemoglobin 9.0g/dl, C-reactive protein 22.9mg/dl, fasting blood glucose 335mg/dl, glycosylated hemoglobin 8.1%, blood urea nitrogen 23.7mg/dl, creatinine 0.73mg/dl, glutamic-oxaloacetic transaminase 59IU/l, glutamic-pyruvic transaminase 62IU/l, cholinesterase 134IU/l, alkaline phosphatase 600IU/l, lactate dehydrogenase 381IU/l, and creatine kinase 566IU/l. US examination of the left SCJ suggested pyogenic arthritis with involvement of the sternocleidomastoid muscle. The chest X-ray was normal, and there were no abnormalities on ECG or cardiac US. CT showed erosion and abscess formation of the SCJ with extension of the abscess into the mediastinum (Figures1A and ​and1B)1B) and sternocleidomastoid muscle (Figure1C). Abdominal CT showed swelling of the left paraspinal muscle at L1-L3 (Figure2A). MRI showed spondylitis of the L3-L4 vertebrae (Figure2B) with a focal epidural collection and L3-L4 discitis (Figure2C).

Aspiration of the SCJ revealed a turbid fluid (approximately 3ml) (Figure3) with clusters of gram-positive cocci on microscopy. The SCJ was incised and drained, and the abscess cavity was enlarged to include the abscess of the left sternocleidomastoid muscle. Sulbactam/ampicillin administration was started immediately. Aspirated pus, urine, and two sets of blood cultures all indicated S. aureus infection. According to the results of antibiotic susceptibility testing, the patient’s antibiotic therapy was changed to cefotiam. After one week of antibiotic therapy, blood and wound cultures were negative for pathogens. Follow-up MRI clearly showed abscess formation in the left paraspinal muscle at L1-L3, but culture of fluid aspirated from the abscess showed no growth.

Septic arthritis most commonly affects the weight-bearing joints of the lower limb, which account for 61-79% of all reported cases of septic arthritis [8]. The knee is the most commonly affected joint, followed by the hip, shoulder, wrist, ankle, and elbow. There is usually no limiting basement plate under the well-vascularized synovial membrane, facilitating the entry of hematogenously carried bacteria into the joint space [9].

Septic arthritis of the SCJ is extremely rare, comprising 0.5–1% of all joint infections [10], but results in abscess formation in 20% of cases [11,12]. The SCJ is the only joint connecting the trunk with the pectoral girdle, and is therefore involved in all major movements of the upper limb. The function of the articular disc on the clavicular side of the SCJ is to resist the compressive load [13]. SCJ infection can cause life-threatening complications, because the joint capsule is unable to distend and infection spreads beyond the joint quickly, leading to fistula formation, cutaneous abscess or, rarely, mediastinitis and superior vena cava syndrome [14,15].

The pathogenesis of SCJ infection is not well understood, but it appears to result from either hematogenous or contiguous spread. Various factors have been identified as predisposing to the development of SCJ infections, including immunocompromising diseases such as diabetes, rheumatoid arthritis, renal dysfunction, and human immunodeficiency virus infection [6].The SCJ can be seeded with microorganisms via the subclavian vein following injection into the veins of the upper extremity or neck (including intravenous drug abuse), clavicular fractures, subclavian vein catheterization, or scratches or animal bites to the hand or arm [6,16]. SCJ infection is generally unilateral, affecting the right side in approximately 60% of cases. This difference in occurrence between sides is less apparent in intravenous drug abusers [4,17]. According to El Ibrahimi, bacteremia was the most commonly assumed mechanism of infection [17]. As in most joints, septic arthritis of the SCJ is most commonly caused by S. aureus, followed by pseudomonas species [18,19]. If an abscess develops, drainage and thorough debridement are necessary. Excision of the medial end of the clavicle, first rib, and manubrium may be required, which usually leaves a large chest wall defect, and exposes major vessels. This defect can be repaired with an advancement or rotational flap of the pectoralis major muscle [20].

Paraspinal muscle infection, a pyogenic infection of skeletal muscle, is rarely reported. Modes of infection include transcutaneous infection by needles or catheters, surgery, blunt trauma, and hematogenous spread from distant sites.

Spondylodiscitis, a term encompassing vertebral osteomyelitis, spondylitis, and discitis, is a rare medical emergency. Spinal epidural abscess is also uncommon, and requires early detection and appropriate treatment to prevent severe morbidity and mortality [21-24]. About 5% of patients with spinal epidural abscesses die, usually because of uncontrolled sepsis, meningitis, or other underlying illnesses [22]. In 25-50% of cases, spondylodiscitis is associated with an epidural abscess or granulation tissue. Pyogenic spondylodiscitis with an epidural abscess may progress to a severe neurological deficit, especially if the diagnosis is established late and it is complicated by the development of an intramedullary abscess of the spinal cord [21].

Hematogenous osteomyelitis usually occurs in patients over 50years of age and accounts for 3-5% of all cases of osteomyelitis. The incidence of hematogenous osteomyelitis is estimated to be 4 to 24 per million per year in developed countries. Pathogens may infect the spine via three routes: hematogenous spread, direct external inoculation, and spread from contiguous tissues [25]. Spontaneous pyogenic spondylodiscitis usually spreads hematogenously from infections of the skin, subcutaneous tissues, or urinary tract [5]. The hematogenous arterial route predominates, allowing seeding of infection from distant sites to the vertebral column [25]. The most common causative pathogen is Staphylococcus aureus, followed in frequency by BrucellaSalmonella, and Mycobacterium tuberculosis[21,26]. The most likely portal of entry in cases of S. aureus infection is the skin (particularly from the skin creases between the toes). Unlike urinary tract infections caused by other pathogens, those caused by S. aureus are most often due to hematogenous dissemination. The presence of S. aureus in the urine, as in this case, therefore suggests hematogenous spread of infection [27]. S. aureusStreptococcus species, and N. gonorrhoeae have a high degree of selectivity for the synovium, probably related to adherence characteristics and toxin production [9].