"Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing that ever has."

Margaret Mead
Case report
peer-reviewed

Mycobacterial Osteomyelitis of the Spine Following Intravesical BCG Therapy for Bladder Cancer



Abstract

Osteomyelitis is an infection of the bone that can involve the vertebral column. A rare cause of vertebral osteomyelitis is Mycobacterium bovis after intravesical Bacillus Calmette-Guerin (BCG) therapy for transitional cell carcinoma of the bladder. In this report, we describe the case of a 64-year-old male presenting with constitutional symptoms, progressive thoracic kyphosis, and intractable T11 and T12 radiculopathies over the proceeding six months. A CT scan revealed erosive, lytic changes of the T12 and L1 vertebrae with compression of the T12 vertebra. An MRI demonstrated T11-12 osteomyelitis with intervening discitis and extensive paraspinal enhancement with a corresponding hyperintensity on a short tau inversion recovery (STIR) sequence. A needle aspiration grew out Mycobacterial tuberculosis complex that was pansensitive to all antimicrobial agent therapies, except pyrazinamide on culture, a finding consistent with an M. bovis infection. The patient’s infection and neurologic compromise resolved after transthoracic T11-12 vertebrectomies with decompression of the spinal cord and nerve roots as well as T10-L1 instrumented fusion and protracted antimicrobial therapy. The epidemiology and natural history of M. bovis osteomyelitis are reviewed and the authors emphasize a mechanism of vertebral inoculation to explain the predilection of M. bovis osteomyelitis in males after intravesical BCG therapy.

Introduction

The incidence of vertebral osteomyelitis is currently estimated to be about 2.5/100,000, but this figure continues to increase [1]. Vertebral osteomyelitis is foremost a bacterial infection. The most common pyogenic pathogens include Staphylococcus aureus, Escherichia coli, and coagulase-negative Staphylococcus species. However, other etiologies have also been reported [2].

In developed countries, tuberculosis may be responsible for 9-46% of vertebral osteomyelitis [2]. Also known as Pott’s disease, tuberculous osteomyelitis typically affects the intervertebral disc space and adjoining vertebrae within the thoracolumbar region [3]. Although the predominant agent of Pott’s disease is Mycobacterium tuberculosis, the zoonotic pathogen, Mycobacterium bovis, can also infect humans, resulting in both pulmonary and vertebral disease. Current estimates suggest that M. bovis accounts for 1-2% of all TB cases reported in developed countries [4].

A live-attenuated strain of M. bovis, Bacillus Calmette–Guérin (BCG), was initially developed as a vaccine for the human form of TB but has proven to be a safe and effective therapy for various carcinomas in situ. Since 1976, BCG has been administered intravesically to treat transitional cell carcinoma of the bladder [5]. It is believed that the BCG mycobacteria adhere to the bladder wall and stimulate a Th1-mediated immune response, which diminishes tumor burden, by releasing interferons and recruiting natural killer cells [6]. Less than 5% of the patients treated with this technique experience a drug-related adverse event during therapy [7]. The most frequent side effects are local, namely cystitis and bladder contractures [8]. Injury to the bladder endothelium during or after treatment appears to be a prerequisite for disseminated morbidities [8]. Vertebral osteomyelitis is a rare – but serious – potential complication of intravesical BCG instillation [5]. Herein, we describe a particularly severe episode of BCG-induced tuberculous osteomyelitis. Informed patient consent was obtained for his treatment.

Case Presentation

A 64-year-old male with a medical history of transitional cell carcinoma of the bladder treated with intravesical BCG over two months presented with a six-month history of severe, progressive mid-back and chest wall pain. He had become non-ambulatory and also began to display constitutional symptoms, including night sweats and weight loss. For his oncologic care, he had undergone two transurethral resections six and 11 months prior to presentation, which had been interspaced by five instillations of intravesical BCG.

The patient first presented to an outside hospital with complaints of mid-back pain six months prior to presentation. Laboratory data was notable for a moderately elevated white blood cell count of 22.1 K/μL, a C-reactive protein of 40.42 mg/L, and an erythrocyte sedimentation rate of 23 mm/hr. A chest x-ray revealed multiple, nonspecific lung nodules which were inconsistent with pulmonary tuberculosis. A subsequent CT scan revealed erosive, lytic changes of the T11 and T12 vertebrae with compression of the T11 vertebra (Figure 1).

An MRI scan demonstrated T11-12 osteomyelitis with intervening discitis, paraspinal enhancement, and corresponding hyperintensity on a short tau inversion recovery (STIR) sequence consistent with an infectious process (Figure 2) [9]. A CT-guided needle aspiration yielded a negative gram stain and acid-fast bacillus (AFB) smear but grew Mycobacterial tuberculosis complex that was pansensitive to all therapies, except pyrazinamide on culture, a result characteristic of an M. bovis infection [10].

The patient began antimicrobial therapy that included rifabutin, ethambutol, isoniazid, and capreomycin. Capreomycin was discontinued due to renal insufficiency; cycloserine and moxifloxacin were ultimately added to the regimen in its place. Despite this aggressive antimicrobial therapy, the patient’s infection demonstrated radiographic evolution over the next two months, at which point he was evaluated by our institution. He had developed progressive kyphosis with intractable T11 and T12 radiculopathies due to nerve root compression, and surgical intervention was recommended. The patient underwent transthoracic T11-L2 vertebrectomies with decompression of the spinal cord and nerve roots as well as a T10-L1 instrumented fusion. After surgery, the patient was immobilized in a thoracolumbosacral orthosis (TLSO) brace and referred to physical therapy for 12 weeks with continued antimicrobial therapy consisting of rifabutin, ethambutol, isoniazid, cycloserine, and moxifloxacin.

The patient reported dramatic improvement in his pain and the ability to ambulate with a cane eight months postoperatively. Imaging studies 12 months postoperatively demonstrated continued remission of any infection and stable instrumentation (Figure 3). At the recommendation of our infectious disease service, his antimicrobial regimen was maintained and will likely be maintained for about one year in total.

Discussion

In this case, we postulated that the intravesical BCG treatments had introduced an M. bovis infection, which had disseminated to cause vertebral osteomyelitis following the localized trauma of the second transurethral resection [5].

A review of the literature revealed 16 cases of M. bovis vertebral osteomyelitis secondary to intravesicular BCG therapy [5, 8, 11-24]. To appropriately evaluate the etiology of the cases, the review was restricted to the English language. All cases occurred in men between the ages of 58 and 94 with a time of onset ranging from two weeks to 12 years following BCG treatment. The most commonly affected vertebrae were T6-L5. As in our case, the axial back pain was the primary complaint. Weight loss [5, 8, 12, 20-21, 23-24] or lower extremity radiculopathies [8, 12, 14, 19-21] were secondary complaints in 9/16 cases. Antimicrobial TB therapy avoided surgical intervention in 9/16 cases [11, 13, 15-18, 20-22]. Isoniazid and rifampicin were the first-line agents of choice for M. bovis, frequently combined with ethambutol [5, 8, 13, 16-17, 20-23] and occasionally concomitant second-line agents [18, 21].

Potential trauma to the bladder endothelium (unrelated to BCG instillation) was described in 7/16 cases [13, 15-18, 22-23]. Such trauma included a biopsy or resection of the bladder [15-16, 22], pelvic radiation [17], radical cystoprostatectomy [13, 16], endovascular aneurysm repair of the abdominal aorta [18], and motor vehicle accident [23]. In the remaining nine cases, BCG instillation itself and the related instrumentation was considered to be the most likely source of endothelial trauma [5, 8, 11-12, 14, 19-21, 24].

Clinicians should be aware that traumatic intravesicular BCG therapy is not the sole mechanism of M. bovis spinal tuberculosis in adults. Alternative routes of entry include bovine contact and unpasteurized milk ingestion [25-27], adolescent BCG vaccination [28], intralesional BCG for non-bladder carcinoma [29], and incidental occupational exposure during BCG administration [30]. These cases have a wider age range (31-72 years old), frequently affect both sexes, and may involve cervical [30] or sacral [25] vertebrae.

The urinary tract is a major source of acute vertebral osteomyelitis [31-33]. Batson’s plexus may be responsible for the venous translocation of urinary tract infections to the internal vertebral venous column [34]. Others have previously speculated that intravesical BCG follows this hematogenous path when precipitating tuberculous spondylitis [5].

Despite the prevalence of genitourinary tract infections in women, vertebral osteomyelitis secondary to urinary tract infections most frequently occur in elderly men [34]. In fact, no cases of female vertebral osteomyelitis following intravesical BCG have been described in the English literature. Since bladder cancer is four times as common in men than women [35], a higher prevalence of case reports describing male patients is to be expected. However, male and female bladder cancer patients receive at least some form of intravesical BCG therapy at similar frequencies [36]. It is, therefore, curious that every known case of intravesical BCG-induced spondylitis occurred in a male.

This disproportion may be due to the presence of the prostatic venous plexus in men. In males, the vesical venous plexus may drain into the prostatic venous plexus, offering a direct path to the vertebral venous plexus. Females have no corresponding structure. Thus, urinary tract infections in females must take a much more circuitous route to the vertebral bodies via the internal iliac veins. These anatomic variances between genders may explain the disproportionately greater number of male cases of BCG osteomyelitis.

No formal American guidelines exist for managing vertebral osteomyelitis. As-directed antimicrobial therapy often resolves osteomyelitis without the need for surgery, initial treatment should be pathogen-directed [1]. Pyrazinamide-resistant tuberculosis, such as M. bovis, is most commonly treated with two months of isoniazid, rifampicin, and ethambutol followed by seven additional months of isoniazid and rifampicin. When TB suspicion is high, therapy should begin empirically after cultures have been obtained [10]. Pathologic deterioration despite antimicrobial therapy may require debridement and instrumentation may be necessary if the stability of the vertebral column is compromised [37]. Indications for surgical debridement, spinal decompression, and stabilization include the progression of infection despite antimicrobial therapy, spine deformity (e.g., kyphosis), pathologic fracture with intractable pain, and neurologic compromises, such as myelopathy and radiculopathy.

Conclusions

A rare cause of vertebral osteomyelitis is Mycobacterium bovis after intravesical BCG therapy for transitional cell carcinoma of the bladder. In males, the vesical venous plexus can drain into the prostatic venous plexus and offer a direct path of hematogenous spread to the vertebral venous plexus. Despite aggressive antimicrobial therapy, M. bovis may demonstrate radiographic evolution with worsening neurological sequelae. Surgical debridement and vertebrectomies with instrumented fusion at the affected levels can help reduce the infection and improve clinical symptoms.


References

  1. Zimmerli W: Clinical practice. Vertebral osteomyelitis. N Engl J Med. 2010, 362:1022–29. 10.1056/NEJMcp0910753
  2. Gouliouris T, Aliyu SH, Brown NM: Spondylodiscitis: update on diagnosis and management. J Antimicrob Chemother. 2010, 65:iii11-24. 10.1093/jac/dkq303
  3. Garg RK, Somvanshi DS: Spinal tuberculosis: a review. J Spinal Cord Med. 2011, 34:440-54. 10.1179/2045772311y.0000000023
  4. Hlavsa MC, Moonan PK, Cowan LS, Navin TR, Kammerer JS, Morlock GP, Crawford JT, Lobue PA: Human tuberculosis due to Mycobacterium bovis in the United States, 1995-2005. Clin Infect Dis. 2008, 47:168-75. 10.1086/589240
  5. Obaid S, Weil AG, Rahme R, Gendron C, Shedid D: Mycobacterium bovis spondylodiscitis after intravesical Bacillus Calmette-Guérin therapy. Surg Neurol Int. 2011, 2:162.
  6. Böhle A, Brandau S: Immune mechanisms in bacillus Calmette-Guerin immunotherapy for superficial bladder cancer. J Urol. 2003, 170:964–69. 10.1097/01.ju.0000073852.24341.4a
  7. Lamm DL: Efficacy and safety of bacille Calmette-Guérin immunotherapy in superficial bladder cancer. Clin Infect Dis. 2000, 3:S86-90. 10.1086/314064
  8. Mavrogenis AF, Sakellariou VI, Tsiodras S, Papagelopoulos PJ: Late Mycobacterium bovis spondylitis after intravesical BCG therapy. Joint Bone Spine. 2009, 76:296–300. 10.1016/j.jbspin.2008.10.011
  9. Burrill J, Williams CJ, Bain G, Conder G, Hine AL, Misra RR: Tuberculosis: a radiologic review. Radiographics. 2007, 27:1255-73. 10.1148/rg.275065176
  10. American Thoracic Society; CDC; Infectious Diseases Society of America: Treatment of tuberculosis. MMWR Recomm Rep. 2003, 52:1–77.
  11. Samadian S, Phillips FM, Deeab D: Mycobacterium bovis vertebral osteomyelitis and discitis with adjacent mycotic abdominal aortic aneurysm caused by intravesical BCG therapy: a case report in an elderly gentleman. Age Ageing. 2013, 42:129–31. 10.1093/ageing/afs164
  12. Katz DS, Wogalter H, D'Esposito RF, Cunha BA: Mycobacterium bovis vertebral osteomyelitis and psoas abscess after intravesical BCG therapy for bladder carcinoma. Urology. 1992, 40:63–66. 10.1016/0090-4295(92)90439-4
  13. Colebatch AN, Mounce KE: Mycobacterium bovis discitis as a complication of intravesical Bacillus Calmette-Guérin therapy. J Clin Rheumatol. 2010, 16:74–75. 10.1097/RHU.0b013e3181d070ea
  14. Dahl T, Lange C, Ødegård A, Bergh K, Osen SS, Myhre HO: Ruptured abdominal aortic aneurysm secondary to tuberculous spondylitis. Int Angiol. 2005, 24:98–101.
  15. Fishman JR, Walton DT, Flynn NM, Benson DR, deVere White RW: Tuberculous spondylitis as a complication of intravesical bacillus Calmette-Guerin therapy. J Urol. 1993, 149:584–87.
  16. Patel AR, Sabanegh ES, Jones JS, Gordon SM, Ballin M, Ruggieri PM, Stephenson AJ: Bacillus Calmette-Guérin osteomyelitis mimicking spinal metastasis from urothelial cell carcinoma of the bladder. Eur Urol. 2010, 58:934–37. 10.1016/j.eururo.2009.05.045
  17. Nikaido T, Ishibashi K, Otani K, Yabuki S, Konno S, Mori S, Ohashi K, Ishida T, Nakano M, Yamaguchi O, Suzutani T, Kikuchi S: Mycobacterium bovis BCG vertebral osteomyelitis after intravesical BCG therapy, diagnosed by PCR-based genomic deletion analysis. J Clin Microbiol. 2007, 45:4085-87. 10.1128/jcm.01714-07
  18. Santbergen B, Vriens PH, de Lange WC, Van Kasteren ME: Combined infection of vertebroplasty and aortic graft after intravesical BCG treatment. BMJ Case Rep. 2013, 2013:pii: bcr2012008161. 10.1136/bcr-2012-008161
  19. Aljada IS, Crane JK, Corriere N, Wagle DG, Amsterdam D: Mycobacterium bovis BCG causing vertebral osteomyelitis (Pott's disease) following intravesical BCG therapy. J Clin Microbiol. 1999, 37:2106–108.
  20. Abu-Nader R, Terrell CL: Mycobacterium bovis vertebral osteomyelitis as a complication of intravesical BCG use. Mayo Clin Proc. 2002, 77:393–97. 10.4065/77.4.393
  21. Rozenblit A, Wasserman E, Marin ML, Veith FJ, Cynamon J, Rozenblit G: Infected aortic aneurysm and vertebral osteomyelitis after intravesical bacillus Calmette-Guérin therapy. AJR Am J Roentgenol. 1996, 167:711–13. 10.2214/ajr.167.3.8751686
  22. Josephson CB, Al-Azri S, Smyth DJ, Haase D, Johnston BL: A case of Pott's disease with epidural abscess and probable cerebral tuberculoma following Bacillus Calmette-Guérin therapy for superficial bladder cancer. Can J Infect Dis Med Microbiol. 2010, 21:e75-78.
  23. Morgan MB, Iseman MD: Mycobacterium bovis vertebral osteomyelitis as a complication of intravesical administration of Bacille Calmette-Guérin. Am J Med. 1996, 100:372–73. 10.1016/s0002-9343(97)89500-9
  24. Civen R, Berlin G, Panosian C: Vertebral osteomyelitis after intravesical administration of bacille Calmette-Guérin. Clin Infect Dis. 1994, 18:1013–14.
  25. Ahmad N, Srinivasan K, Panayi J, Moudgil H: Lumbo-sacral spine disease due to bovine tuberculosis in a patient with concurrent pulmonary disease. Prim Care Respir J. 2011, 20:459–61. 10.4104/pcrj.2011.00037
  26. Schübel N, Rupp J, Gottschalk S, Zabel P, Dalhoff K: Disseminated mycobacterium bovis infection in an immunocompetent host. Eur J Med Res. 2006, 11:163–66.
  27. Steensels D, Fauville-Dufaux M, Boie J, De Beenhouwer H: Failure of PCR-Based IS6110 analysis to detect vertebral spondylodiscitis caused by Mycobacterium bovis. J Clin Microbiol. 2013, 51:366–68. 10.1128/JCM.02524-12
  28. Rätsep T: Postoperative spondylodiscitis caused by Mycobacterium bovis BCG: a case study. Spine J. 2012, 12:e1-5. 10.1016/j.spinee.2012.10.024
  29. Strausser JL, Quindlen EA: Pott's disease following BCG therapy of melanoma. Cancer. 1981, 48:1154–56. 10.1002/1097-0142(19810901)48:5<1154::AID-CNCR2820480519>3.0.CO;2-0
  30. Titlić M, Išgum V, Buca A, Kolić K, Tonkić A, Jukić I, Milas I: Somatosensory-evoked potentials and MRI in tuberculous spondylodiscitis. Bratisl Lek Listy. 2007, 108:153–57.
  31. Krogsgaard MR, Wagn P, Bengtsson J: Epidemiology of acute vertebral osteomyelitis in Denmark: 137 cases in Denmark 1978-1982, compared to cases reported to the National Patient Register 1991-1993. Acta Orthop Scand. 1998, 69:513–17. 10.3109/17453679808997789
  32. Carragee EJ: Pyogenic vertebral osteomyelitis. J Bone Joint Surg Am. 1997, 79:874–80.
  33. Mylona E, Samarkos M, Kakalou E, Fanourgiakis P, Skoutelis A: Pyogenic vertebral osteomyelitis: a systematic review of clinical characteristics. Semin Arthritis Rheum. 2009, 39:10–17. 10.1016/j.semarthrit.2008.03.002
  34. Sapico FL, Montgomerie JZ: Pyogenic vertebral osteomyelitis: report of nine cases and review of the literature. Rev Infect Dis. 1979, 1:754–76. 10.1093/clinids/1.5.754
  35. Kirkali Z, Chan T, Manoharan M, Algaba F, Busch C, Cheng L, Kiemeney L, Kriegmair M, Montironi R, Murphy WM, Sesterhenn IA, Tachibana M, Weider J: Bladder cancer: epidemiology, staging and grading, and diagnosis. Urology. 2005, 66:4–34. 10.1016/j.urology.2005.07.062
  36. Huang GJ, Hamilton AS, Lo M, Stein JP, Penson DF: Predictors of intravesical therapy for nonmuscle invasive bladder cancer: results from the surveillance, epidemiology and end results program 2003 patterns of care project. J Urol. 2008, 180:520–24. 10.1016/j.juro.2008.04.016
  37. Chen WH, Jiang LS, Dai LY: Surgical treatment of pyogenic vertebral osteomyelitis with spinal instrumentation. Eur Spine J. 2007, 16:1307–16. 10.1007/s00586-006-0251-4
Case report
peer-reviewed

Mycobacterial Osteomyelitis of the Spine Following Intravesical BCG Therapy for Bladder Cancer


Author Information

Charles E. Mackel Corresponding Author

Department of Neurosurgery, Tufts University School of Medicine/Tufts Medical Center

Shane M. Burke

Department of Neurosurgery, Tufts University School of Medicine/Tufts Medical Center

Taylor Huhta

Department of Neurosurgery, Tufts University School of Medicine/Tufts Medical Center

Ron Riesenburger

Department of Neurosurgery, Tufts University School of Medicine/Tufts Medical Center

Simcha J. Weller

Department of Neurosurgery, Tufts University School of Medicine/Tufts Medical Center


Ethics Statement and Conflict of Interest Disclosures

Human subjects: Consent was obtained by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.


Case report
peer-reviewed

Mycobacterial Osteomyelitis of the Spine Following Intravesical BCG Therapy for Bladder Cancer


Figures etc.

SIQ
6.6
RATED BY 2 READERS
CONTRIBUTE RATING

Scholary Impact Quotient™ (SIQ™) is our unique post-publication peer review rating process. Learn more here.