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A 45-year-old Indian labourer presented to his general practitioner with chronic low back pain. This had worsened over 4 months and radiated to the left thigh. He denied urinary and faecal incontinence, leg weakness, numbness and paraesthesia. There was no significant past medical history. His general practitioner suspected musculoskeletal injury and arranged a lumbar X-ray to exclude bony abnormalities.
Plain lumbar X-ray showed loss of intervertebral disc space at T12–L1, and an enlarged left psoas shadow (figure 1), appearances concerning for discitis, vertebral collapse and psoas abscess formation. Further imaging was arranged given the patient’s ethnic origin and the high prevalence of tuberculosis (TB) around our urban district general hospital. Chest radiograph showed right middle zone consolidation and pleural effusion. He was urgently referred to our infectious diseases team.
On further questioning, he denied fever, cough, breathlessness and night sweats, but recalled a 4 kg weight loss in the past month. He had emigrated to the UK from India 2 years previously and had not travelled abroad since his arrival. He had no known past contact with TB.
Examination revealed reduced air entry at the right base and tenderness over the L1 vertebra. There was no limb weakness, numbness, reduction in anal tone or palpable abdominal masses. Temperature was 37.8 °C. Blood tests showed mild normocytic anaemia, raised inflammatory markers (C-reactive protein 42) and normal white cell count. HIV and hepatitis B and C serology were negative, and random glucose was measured at 6 mmol/L.
Computed tomography (CT) imaging of the abdomen and pelvis confirmed loss of height and end plate destruction of the T12–L1 vertebral bodies, and identified a large, loculated psoas abscess measuring 75×52×120 mm. Purulent fluid (300 mL) was aspirated after ultrasound-guided percutaneous drain insertion. Acid fast bacilli were seen on drain fluid microscopy, and GeneXpert testing was positive for Mycobacterium tuberculosis with no rifampicin resistance. He was started on analgesia, antituberculous therapy and dexamethasone.
Magnetic resonance (MR) imaging of the spine demonstrated a large paravertebral abscess extending from T6 to L1, and an extradural abscess causing mild cord compression (figure 2). He was fitted with a spinal brace on the advice of the neurosurgical team. Repeat ultrasound imaging confirmed resolution of his psoas abscess and he was discharged home with analgesia, antituberculous therapy and a weaning steroid regimen. Interval MR scan at 9 months showed a reduction in the size of the collection at T12–L1. He completed a 12 month course of treatment and has returned to work.
This immunocompetent patient presented with vague low back pain, illustrating the diagnostic challenge posed by spinal TB. A total of 147 cases of spinal TB were recorded in England in 2018, representing 3.2% of cases.1 Despite extensive disease, our patient was afebrile and continued to walk unaided at the time of diagnosis. Mycobacterial psoas abscesses are uncommon, usually resulting from contiguous spread from spinal TB.1 Although CT imaging is sensitive in identifying psoas abscesses,2 MR imaging is the preferred modality in patients with spinal involvement to inform the need for neurosurgical intervention.3
Spinal tuberculosis (TB) is an important differential diagnosis for back pain, particularly in young and middle aged adults hailing from hyperendemic settings.
Psoas abscess is a rare manifestation of extrapulmonary TB, usually resulting from contiguous spread from a spinal source.
Spinal column stability is an important consideration in patients with spinal TB.
Contributors CHC conceived the article and obtained the patient’s written consent. CHC and JP wrote the first draft. AR performed image guided percutaneous drainage of the patient’s psoas abscess and sourced high quality images for this report. WL and AR critically reviewed the manuscript for accuracy and intellectual content. All authors revised subsequent drafts and approved the final version of the article.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent for publication Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.
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