Introduction
Tuberculosis (TB) remains a leading infectious cause of death worldwide [
1]. Once on the decline and almost eradicated in industrialized countries, TB is re-emerging as a major public health threat. Skeletal TB accounts for approximately 1%–2% of all infected patients [
2]. The spine is the most common site for skeletal TB, accounting for 50% of cases [
3].
Continuous vertebral involvement is the most common disease pattern [
4]. Noncontiguous multiple-level spinal tuberculosis (NMLST) is an atypical and rare form of spinal TB. It is defined as vertebral disease in addition to the primary lesion, with diseased spinal segments separated by at least one normal spinal segment. There is large variability in the reported incidence of NMLST, ranging from 1.1% to 71.4% [
4,
5]. In the present study, we sought to discuss the role of whole-spine screening using short tau inversion recovery (STIR) or fat-suppressed T2W fast spin echo (FSE) magnetic resonance imaging (MRI) sequences in patients with signs and symptoms suggestive of spinal TB.
Materials and Methods
1. Patients
We completed a retrospective review of clinical and radiographic data that were prospectively collected on 365 patients with spinal TB who were diagnosed and treated at Jawaharlal Nehru Medical College Hospital, Aligarh, from January 2010 to January 2015. The ethical committee of the Jawaharlal Nehru Medical College Hospital approved the study and informed consent was waived. Inclusion criteria included available whole-spine MRI performed on admission and confirmation of vertebral TB by histology, microbiology, or positive response to anti-tubercular treatment.
The primary site was defined as the site for which the patient had been referred for MRI. Diagnosis of NMLST was considered when other vertebral lesions were identified in addition to the primary vertebral disease, with the lesions separated by at least one normal spinal segment.
2. Diagnosis
Diagnosis was confirmed after open surgical biopsy or image-guided percutaneous needle biopsy by histology or microbiology. Histological evaluation of biopsy samples was performed to look for granulomas, Langhans giant cells, and caseous necrosis. Microscopic examination was performed to check for acid-fast bacilli. Specimens were cultured for a total of 6 weeks before being declared negative. For patients where a tissue confirmation of TB was not available, a positive response to anti-tubercular treatment was considered diagnostic. The MRI protocol varied among patients but for the most part included the following pulse sequences: T1W, T2W in the sagittal plane, STIR in the coronal plane, and axial T1W and T2W. Post-contrast fat-suppressed T1W images were obtained in three orthogonal planes.
3. Statistics analysis
The statistical analysis was performed using Microsoft Excel (Microsoft Corp., Redmond, WA, USA) and SPSS software ver. 16.0 (SPSS Inc., Chicago, IL, USA).
Results
Of 365 patients with spinal TB, only 187 met the inclusion criteria and were included in the final review. This was largely due to the non-availability of whole-spine MRI. The average age was 37 years (range, 7–81 years), with 18 females and 29 males. The incidence of NMLST in patients investigated using whole-spine MRI was 25.1% (47/187 patients). The remaining 140 patients showed single or contiguous spinal lesions. Their average age was 29 years (range, 4–82 years), with 63 females and 77 males. Concurrent pulmonary TB was identified in 39 of 187 patients. The two groups were not statistically different when compared for age, sex, and outcome.
The diagnosis of TB was made with microbiology in 108 patients and histopathology in 72 patients. In 28 patients, both microbiology and histopathology were available. In 35 patients, a presumptive diagnosis was made based on a positive response to anti-tubercular treatment. MRI revealed at least one typical TB lesion in all 187 patients. These included intervertebral disc narrowing, T2 hyperintensity and heterogeneous pattern of contrast enhancement of involved vertebral bodies, posterior element involvement, subligamentous spread, epidural extension, and presence of paraspinal or intraosseous abscess (
Figs. 1,
2). Of the 47 patients with multiple level involvement, all had clear evidence of noncontiguous lesions on MRI.
With regard to the distribution of lesions, 37 patients had two noncontiguous foci involved, while the remaining 10 patients had three or more discrete lesions. The distribution of involved vertebrae showed a predilection for the lower thoracic and lumbosacral vertebrae, in keeping with distribution patterns described by Hodgson. The lumbar spine was involved in 37 patients, thoracic spine in 25, cervical spine in 16, and sacrum in five. Combined lumbar spine and thoracic spine involvement was observed in 19 patients, lumbar and cervical spine involvement in 13, thoracic and cervical spine involvement in nine, and combined lumbar and sacral spine involvement in four, while the remaining two patients showed thoracic and sacral spine involvement (
Table 1).
Discussion
TB is the leading infectious cause of mortality and morbidity in developing and third world countries. TB is making a dramatic comeback in industrialized countries as a result of increased immigration, acquired immunodeficiency syndrome, and new drug-resistant strains [
6]. The spine is the most common site of osseous TB due to the hematogenous spread of the infection [
7]. The other mechanisms underlying spinal TB involvement include venous seeding, lymphatic spread, and direct invasion from adjacent viscera or lymph nodes. The infection typically starts in the anterior aspect of the vertebral body adjacent to the intervertebral disc and then spreads to the vertebral bodies under the longitudinal ligaments involving multiple adjacent vertebrae [
6,
8-
10].
NMLST due to the involvement of remote vertebrae is uncommon. The proposed mechanism is through the valveless vertebral venous system, which allows the bacilli to travel to new vertebrae and establish noncontiguous lesions without being filtered through the lungs or lymph nodes. Another explanation is the preferential hematogenous seeding of different spinal segments, but this explanation is less accepted [
6].
The identification of NMLST, symptomatic or not, is important because it influences the treatment approach [
4]. Anti-tubercular chemotherapy is considered the mainstay of treatment for uncomplicated spinal TB. It also improves surgical outcomes by promoting healing and reducing recurrence [
11].
There is a paucity of information regarding the treatment of NMLST. However, the presence of noncontiguous lesions influences decisions surrounding surgical instrumentation and the number of levels instrumented. In addition, if a level is not surgically treated, there may be a need for bracing. The aim of our study was to identify unsuspected sites of disease so that these sites could be monitored and supportive measures could be directed to these sites, thereby potentially preventing pathological fractures or the need for surgery.
Due to the rarity of NMLST, our literature review yielded mostly case reports. The reported incidence of NMLST is highly variable, ranging from 1.1% to 71.4% [
4,
5]. This is likely due to the different types of imaging modalities used, including radiography, computed tomography (CT), bone scintigraphy, and/or MRI. The centers that do not routinely perform whole-spine MRI reported a lower incidence. Kaila et al. [
4] reported a very high incidence of 71.4% but admitted that their data likely overestimated the true incidence of NMLST due to the small number of cases presented. Their population could have also been affected by selection bias as their center is a regional referral center for spinal deformities [
4]. In our study, the incidence of NMLST using whole-spine MRI was 25.1%. The thoracic and lumbar spine were most commonly affected, similar to previous reports.
MRI is the imaging technique of choice in spinal infections due to its high sensitivity and specificity [
12]. Given its superior contrast resolution, it is useful for identifying contiguous and noncontiguous vertebral involvement. MRI also provides critical information about spinal cord involvement and the extent of epidural extension. CT is less accurate for defining epidural extension but is useful in assessing bone destruction. Bone scan findings are nonspecific, and radiographs are insensitive in patients with early disease.
The reason for the increase in the reported incidence of noncontiguous involvement is not fully understood, but it likely relates to the increased use of whole-spine MRI, as in our study. Although it is not always possible and also not necessary to routinely use all sequences of wholespine MRI, we strongly recommend whole-spine screening using STIR or fat-suppressed T2W FSE sequences in all patients with signs or symptoms suggestive of spinal TB. The cost–benefit ratio is good, as our recommendation is not to perform whole-spine MRI utilizing all the sequences but just to screen the spine in a single sagittal plane utilizing a single T2W or STIR sequence. These are FSE sequences and therefore will not substantially increase scan time. The patient turnover time is not increased; therefore, the cost of the MRI should remain unchanged as well.
Conclusions
The identified incidence of NMLST was 25.1% in our study. The prevalence of NMLST in other populations may not be the same as that revealed in our study group given the wide disparity in disease prevalence between developing and developed countries. However, there is a trend toward a higher reported incidence of NMLST compared with continuous vertebral involvement. This trend may not necessarily reflect increasing incidence of disease but instead may reflect increased detection due to the more widespread use of MRI. MRI scanning is much more sensitive than plain radiography for detecting NMLST. The identification of NMLST is important because a large proportion of the affected noncontiguous sites may be asymptomatic. The identification of such asymptomatic sites can alter the therapeutic strategy and thereby limit the morbidity caused by TB. We strongly recommend that the entire spine be screened in patients with TB using STIR or fat-suppressed T2W FSE MRI sequences.
Conflict of Interest
No potential conflict of interest relevant to this article was reported.
Fig. 1.
Sagittal T2W (A), T1W (B), and post-contrast fat-suppressed T1W (C) sequences reveal noncontiguous multiple-level spinal tuberculosis involvement at T9–T10 and L4–L5 levels. Additional enhancing foci of infection were seen in L3 vertebra and conus medullaris.
Fig. 2.
Coronal short tau inversion recovery (A) and post-contrast fatsuppressed T1W (B) sequences reveal noncontiguous multiple-level spinal tuberculosis involvement at T9–T10 and L4–L5 levels. Para spinal soft tissue and L3 vertebral involvement was also observed.
Table 1.
Region |
No. of patients |
Lumbar spine |
37 |
Thoracic spine |
25 |
Cervical spine |
16 |
Sacrum |
5 |
Lumbar spine and thoracic spine |
19 |
Lumbar and cervical spine |
13 |
Thoracic and cervical spine |
9 |
Lumbar and sacral spine |
4 |
Thoracic and sacral spine |
2 |
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