Spinal tuberculosis is common in endemic regions. Psoas abscess associated with lumbosacral tuberculosis is a common finding in long standing cases. But vague symptoms and signs make the clinical diagnosis of psoas abscess with tuberculous spondylodiscitis a challenge. A 22-year-old married female presented with low backache, anorexia and bilateral swellings in the flank regions. The swellings extended to the upper medial quadrant of the buttocks bilaterally. Abdominal ultrasonography showed bilateral psoas abscesses above inguinal ligaments and extending into buttocks bilaterally after iliac bone erosion Magnetic resonance images showed diffuse spondylodiscitis from L1 to S1 and bilateral psoas abscesses, erosion of the iliac bones and a large subfascial abscess over the gluteal muscles. The communication of the buttock abscess into the retroperitoneum and with the psoas abscess was evident. Operative drainage of abscesses was performed and histological examination showed caseaous necrosis confirming the clinical diagnosis of tuberculosis. Anti-tuberculous therapy was started and continued for 12 months with complete recovery.
Spinal tuberculosis is common in endemic regions [1-3] The psoas muscle is a retroperitoneal muscle that originates from the lateral borders of the 12th thoracic to fifth lumbar vertebrae, and ends as a conjoint tendon with ilacus into the lesser trochanter. [4]. Psoas abscess, first described in 1881 by Mynter [5], is a collection of pus in the psoas compartment, and can be primary or secondary. The long standing vague symptoms and signs make the clinical diagnosis of tuberculous spondylodiscitis with psoas abscess a challenge [1, 3]. We report a unique case of extensive lumbosacaral tuberculous spondylodiscitis accompanied by bilateral psoas abscess, which presented as a bilateral soft-tissue flank mass beneath the skin, after eroding the iliac bones. Although psoas abscess due to spinal tuberculosis has been described, bilateral psoas abscess with such presentation is rare. Here we present three cases of TD that we encountered at our centre from May 2010 to April 2013 and provide a review of published literature of this rare form of osteo-articular tuberculosis.
A 22-year-old married female presented with progressively worsening six months history of low backache, three month history of anorexia and low-grade nocturnal fever, one month history of weight loss and 2 week history of painful bilateral flank swellings. The swellings extended into the upper medial quadrant of the buttocks measuring 10 cm x 7 cm (right side) and 7 cm x 4 cm (left side) (Figure 1). Lumbar lordosis was obliterated with paraspinal muscle spasm but neurological examination was intact. Hip joints were normal without any pseudoflexion deformity. Blood tests showed white blood cell count of 9,200/mm3. ESR was 84mm in 1st hour and C-reactive protein level was 10.14 mg/dl. Aspirates from the swellings were sent for culture and sensitivity, cytology, gram and Ziehl–Neelsen staining. Abdominal ultrasonography showed bilateral psoas abscesses extending into buttocks bilaterally after eroding through iliac bones. Magnetic resonance (MR) images revealed diffuse spondylodiscitis from L1 to S1 and confirmed bilateral psoas abscesses, eroding through iliac bones and presenting as large subcutaneous abscess over the gluteal muscles. The communication of the buttock abscess into the retro peritoneum and the psoas abscess was evident (Figure 2A and 2B). There was no involvement of the adjacent organs such as female genitalia, kidney, ureter, and bowel. Both abscesses were drained surgically and specimens were sent for further examination. However, results of the ordinary bacterial or fungal culture were negative. Cytology for malignant cells was also negative and histological examination revealed caseous necrosis implying tuberculosis. Patient was started on anti-tubercular treatment and discharged home for outpatient follow-up. Anti-tubercular therapy was continued for 12 months and patient had complete recovery.
Psoas abscess is rare [6, 7], and that presenting as an extrapelvic extension is even more rare. Psoas abcess eroding the ilium bilaterally and presenting as an extrapelvic extension has not been reported. However, psoas abscess that extended over the iliac wing and presented as a flank or buttock abscess has been reported in medical literature [8, 9, 10-13]. Although the worldwide incidence was considered to be only 12 cases per year [6, 7], psoas abscess is more frequently diagnosed and reported with the advent of computed tomography (CT) and MR imaging [7, 14]. Psoas abscess is considered primary if the cause is hematogenous from a distant site, and secondary if there is a continuous infectious source from vertebrae, pancreas, kidney, ureter, appendix, bowel or hip joint [6, 7, 15]. Our case was secondary psoas abscess, which extended to the buttock through the eroded iliac bones bilaterally. The skeletal system, which is involved in 1%–10% of patients with tuberculosis, is the most common extrapulmonary site for tuberculous infection. Approximately half of skeletal system tuberculosis cases manifest as spinal diseases and 75% are accompanied by paraspinal abscess [2, 16]. A psoas abscess may form and may extend inferiorly as far as the groin and thigh under the psoas sheath along the the muscle course [3]. Subacute presentation along with nonspecific symptoms and signs makes the diagnosis of psoas abscess difficult [1]. The clinical signs and symptoms may include limping, a positive psoas sign, flexion deformity of the hip joint, fatigue, fever, night sweating, and weight loss [17]. The chronic and insidious nature of tuberculous spondylitis causes late diagnosis of this disease. The susceptibility of the psoas muscle as primary site can be attributed to its rich blood supply and proximity to overlying retroperitoneal lymphatic channels [18, 19]. Because the iliopsoas muscle inserts onto the lesser trochanter of femur, it is possible that the psoas abscess could extend to the medial side of the thigh under the inguinal canal [20] or to the hip joint [21, 22-24]. Extension up to the calf has also been reported [25]. Moreover, piriformis and gluteal abscesses have also been reported [12]. However, extension of the psoas abscess to the buttocks eroding through iliac wing is an extremely rare clinical manifestation. The detection of the hidden psoas abscess requires high level of suspicion and failure to recognize and treat psoas abscess results in considerable morbidity [26]. The most common causative organism of the primary psoas abscess is Staphylococcus aureus whereas enteric organisms are responsible for the secondary type [7, 25, 15]. The spinal tuberculosis was the most common etiology half a century ago [26]. Fungal infection also should be excluded [25, 14, 27]. Other rare causes can be appendicitis, pancreatitis, pyelonephritis or Crohn’s disease [18, 26]. The pathogenic organism could not be identified in our case but was presumed to be Mycobacterium tuberculosis based on clinical presentation, histological diagnosis and response to clinical treatment.
In conclusion, in endemic regions patients with long standing psoas abscess can present as buttock abcesses, although bilateral presentation with perforation of iliac wings is very rare. Multiplanar imaging, especially MR imaging, is a useful diagnostic procedure in defining subtle vertebral disc or vertebral body lesions and in detecting unsuspected paravertebral soft-tissue extension. The abscess in our patient was large and extended to buttocks after eroding through iliac wings, thus demonstrating an additional route of extension of psoas abscess. The patient was treated successfully with open surgical drainage and anti-tubercular therapy.
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