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Mycobacterium Chelonae: Differential Diagnoses & Workup

Author: F Matthew Kuhlmann, MD, Fellow, Division of Infectious Diseases, Washington University School of Medicine
Coauthor(s): Keith F Woeltje, MD, PhD, Associate Professor, Department of Internal Medicine, Division of Infectious Diseases, Washington University School of Medicine
Contributor Information and Disclosures

Updated: Aug 26, 2009

Differential Diagnoses

Actinomycosis
Mycobacterium Haemophilum
Blastomycosis
Mycobacterium Kansasii
Coccidioidomycosis (Infectious Diseases)
Mycobacterium Marinum
Coccidioidomycosis (Pulmonology)
Mycobacterium Xenopi
Cryptococcosis
Nocardiosis
Histoplasmosis
Sporotrichosis
Lung Abscess
Tuberculosis
Mycetoma
Wound Infection
Mycobacterium Avium-Intracellulare
Mycobacterium Fortuitum
Mycobacterium Gordonae

Other Problems to Be Considered

Bacterial osteomyelitis
Contamination/pseudoinfection
Colonization
Cutaneous vasculitis
Fusarium species infection
Phaeohyphomycosis
Prototheca species infection
Pseudallescheria boydii infection

Workup

Laboratory Studies

According to American Thoracic Society (ATS) criteria,11,2 diagnosis of M chelonae lung disease requires (1) pulmonary symptoms with consistent radiographic features (see Imaging Studies), (2) exclusion of other diagnoses (especially tuberculosis), and (3) appropriate microbiological findings.

  • Sputum smear for acid-fast bacilli and culture for mycobacteria
    • Microbiological findings to satisfy ATS diagnostic criteria include the following (at least one must apply):
      • Positive culture from 2 separate sputum samples
      • One positive culture from bronchial wash or lavage
      • A biopsy specimen with appropriate histopathologic features and a positive culture from an associated bronchial wash or biopsy culture
    • Induced sputum samples may be substituted for expectorated sputum samples, but data establishing the effectiveness of this technique are lacking.
    • A single positive isolate may represent a contaminant or a persistent or transient colonizer without pathogenicity.
  • Swab culture for acid-fast bacillus
    • Notifying the microbiology laboratory personnel that an NTM is suspected may help ensure appropriate processing of specimens. Most laboratories use liquid media (eg, BACTEC) for mycobacterial cultures.
    • Swab specimens are less optimal than cultures obtained via aspiration. Consider contacting laboratory personnel for proper procedures regarding adequate specimen collection to increase the yield and significance of cultures.
    • Interpret the result with caution because a single positive culture, especially of a superficial lesion, may represent a contaminant or an "innocent bystander." In one study from Spain, 13 of 24 isolates of M chelonae were deemed of questionable clinical significance12
  • Additional testing if M chelonae or M abscessus infection is discovered
    • An HIV test may be warranted, especially if disseminated disease is diagnosed without an obvious underlying condition.
    • Sweat chloride and/or genetic screening for cystic fibrosis may be warranted if lung infection is found in a relatively young patient (<50 y).
    • A purified protein derivative (of tuberculin) (PPD) test should be considered to assist in ruling out tuberculosis.
  • Susceptibility testing should be performed on all isolates to guide treatment. General susceptibility results reported in the new ATS guidelines are as follows:2
    • Tobramycin - 100%
    • Clarithromycin - 100%
    • Linezolid - 90%
    • Imipenem - 60%
    • Amikacin - 50%
    • Clofazimine and doxycycline - 25%
    • Ciprofloxacin - 20%

Imaging Studies

  • Chest radiography
    • Perform chest radiography if pulmonary symptoms are present. Typical findings are bilateral patchy nodular or cavitary opacities (15% are cavitary) with an upper lobe predominance.
    • Normal chest radiographic findings with a single positive culture suggest that the organism is a contaminant or a transient colonizer and is not clinically significant. However, in the presence of chronic persistent pulmonary symptoms or repeatedly positive culture results, additional testing may be necessary.
  • ChestCT scanning
    • If the patient has significant respiratory symptoms or repeatedly positive cultures for the same organism with a lack of cavitary disease on chest radiography, high-resolution CT scanning is likely indicated.
    • Typical CT scan findings include bronchiectasis or diffuse small nodules; these are often not revealed by routine chest radiography.
    • If the chest radiographic findings are abnormal, chest CT scanning may be performed to obtain better definition of the abnormalities present. Lymphadenopathy may also be detected. This study is not necessary in every case but should be strongly considered.
  • CT scanning of the abdomen and pelvis: This study may be indicated to detect local abscesses, including retroperitoneal abscesses, in disseminated disease, localizing signs or symptoms, or a history of injections in those locations.
  • Bone imaging, MRI, and nuclear imaging
    • These studies may be helpful in detecting suspected osteomyelitis or joint disease, especially in patients with a history of penetrating trauma.
    • Gallium scanning may be useful to screen for supradiaphragmatic lymphadenopathy (intrathoracic or axillary).

Other Tests

  • Erythrocyte sedimentation rate or C-reactive protein assessments may be useful to differentiate colonizer and pathogen, but these are nonspecific tests and the results must be carefully evaluated within the clinical context of the patient.

Procedures

  • Lung procedures
    • Perform bronchoscopy with bronchial washes for acid-fast bacillus (AFB) culture, ideally with transbronchial biopsy, for culture and histology. A bronchioloalveolar lavage may also be useful. Because the diagnosis is usually uncertain at this stage, fungal cultures are typically sent as well.
    • Open or thorascopic lung biopsy may be considered if suspicion is high but diagnostic criteria have not been met. Send specimens for fungal and AFB cultures, as well as histology.
    • A biopsy culture positive for M chelonae or M abscessus is considered diagnostic.
    • The presence of either AFB or granulomas in a lung biopsy or a transbronchial biopsy specimen along with even a single positive culture of sputum or bronchial wash (even in low numbers) is considered diagnostic.
  • Skin tests
    • Perform a biopsy for localized or disseminated skin lesions. Send specimens for AFB and fungal cultures, as well as histology.
    • PPD testing with nontuberculous mycobacterial specific antigens is nonspecific and generally not indicated. These tests are not commercially available.
  • Aspiration biopsy
    • Perform an aspiration biopsy of a localized abscess for culture; this method is preferred over culture via swab of draining abscess fluid.
    • Perform a fine-needle aspiration biopsy of a lymphadenitis for histology and culture.

Histologic Findings

Histologic findings may reveal acute inflammation, microabscesses, granulomatous inflammation, or granulomas (with or without caseation). These findings may be mixed. Special tissue stains for AFB may reveal organisms.

Staging

Contamination, colonization, and localized and disseminated disease are present.

More on Mycobacterium Chelonae

Overview: Mycobacterium Chelonae
Differential Diagnoses & Workup: Mycobacterium Chelonae
Treatment & Medication: Mycobacterium Chelonae
Follow-up: Mycobacterium Chelonae
Multimedia: Mycobacterium Chelonae
References
Further Reading

References

  1. Simmon KE, Pounder JI, Greene JN, Walsh F, Anderson CM, Cohen S. Identification of an emerging pathogen, Mycobacterium massiliense, by rpoB sequencing of clinical isolates collected in the United States. J Clin Microbiol. Jun 2007;45(6):1978-80. [Medline].

  2. [Guideline] Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med. Feb 15 2007;175(4):367-416. [Medline].

  3. Hadjiliadis D, Adlakha A, Prakash UB. Rapidly growing mycobacterial lung infection in association with esophageal disorders. Mayo Clin Proc. Jan 1999;74(1):45-51. [Medline].

  4. Sañudo A, Vallejo F, Sierra M, Hoyos JG, Yepes S, Wolff JC. Nontuberculous mycobacteria infection after mesotherapy: preliminary report of 15 cases. Int J Dermatol. Jun 2007;46(6):649-53. [Medline].

  5. Centers for Disease Control and Prevention. Mycobacterium chelonae infections associated with face lifts--New Jersey, 2002-2003. MMWR Morb Mortal Wkly Rep. Mar 12 2004;53(9):192-4. [Medline].

  6. Vijayaraghavan R, Chandrashekhar R, Sujatha Y, Belagavi CS. Hospital outbreak of atypical mycobacterial infection of port sites after laparoscopic surgery. J Hosp Infect. Dec 2006;64(4):344-7. [Medline].

  7. Chetchotisakd P, Kiertiburanakul S, Mootsikapun P, Assanasen S, Chaiwarith R, Anunnatsiri S. Disseminated nontuberculous mycobacterial infection in patients who are not infected with HIV in Thailand. Clin Infect Dis. Aug 15 2007;45(4):421-7. [Medline].

  8. Centers for Disease Control and Prevention. Nontuberculous Mycobacteria Reported to the Public Health Laboratory Information System by State Public Health Laboratories United States, 1993-1996. [Full Text].

  9. Marras TK, Daley CL. Epidemiology of human pulmonary infection with nontuberculous mycobacteria. Clin Chest Med. Sep 2002;23(3):553-67. [Medline].

  10. Uslan DZ, Kowalski TJ, Wengenack NL, Virk A, Wilson JW. Skin and soft tissue infections due to rapidly growing mycobacteria: comparison of clinical features, treatment, and susceptibility. Arch Dermatol. Oct 2006;142(10):1287-92. [Medline].

  11. American Thoracic Society. Diagnosis and treatment of disease caused by nontuberculous mycobacteria. This official statement of the American Thoracic Society was approved by the Board of Directors, March 1997. Medical Section of the American Lung Association. Am J Respir Crit Care Med. Aug 1997;156(2 Pt 2):S1-25. [Medline].

  12. Esteban J, Fernández Roblas R, García Cía JI, Zamora N, Ortiz A. Clinical significance and epidemiology of non-pigmented rapidly growing mycobacteria in a university hospital. J Infect. Feb 2007;54(2):135-45. [Medline].

  13. Fonseca MT, Fonseca MM, Bicalho R, Hadad DJ. Mycobacterium chelonae synovitis. Pediatr Infect Dis J. Nov 2006;25(11):1086. [Medline].

  14. Tebas P, Sultan F, Wallace RJ Jr, Fraser V. Rapid development of resistance to clarithromycin following monotherapy for disseminated Mycobacterium chelonae infection in a heart transplant patient. Clin Infect Dis. Feb 1995;20(2):443-4. [Medline].

  15. Wallace RJ Jr, Tanner D, Brennan PJ, Brown BA. Clinical trial of clarithromycin for cutaneous (disseminated) infection due to Mycobacterium chelonae. Ann Intern Med. Sep 15 1993;119(6):482-6. [Medline].

  16. Wallace RJ Jr, Swenson JM, Silcox VA, Bullen MG. Treatment of nonpulmonary infections due to Mycobacterium fortuitum and Mycobacterium chelonei on the basis of in vitro susceptibilities. J Infect Dis. Sep 1985;152(3):500-14. [Medline].

  17. Heifets LB. Antimycobacterial drugs. Semin Respir Infect. Jun 1994;9(2):84-103. [Medline].

  18. Brown-Elliott BA, Wallace RJ, Crist CJ, et al. Comparison of in vitro activities of gatifloxacin and ciprofloxacin against four taxa of rapidly growing mycobacteria. Antimicrob Agents Chemother. Oct 2002;46(10):3283-5. [Medline].

  19. Woods GL, Bergmann JS, Witebsky FG, Fahle GA, Wanger A, Boulet B. Multisite reproducibility of results obtained by the broth microdilution method for susceptibility testing of Mycobacterium abscessus, Mycobacterium chelonae, and Mycobacterium fortuitum. J Clin Microbiol. Jun 1999;37(6):1676-82. [Medline].

  20. Brown-Elliott BA, Wallace RJ, Blinkhorn R, et al. Successful treatment of disseminated Mycobacterium chelonae infection with linezolid. Clin Infect Dis. Oct 15 2001;33(8):1433-4. [Medline].

  21. Wallace RJ Jr, Brown-Elliott BA, Ward SC, et al. Activities of linezolid against rapidly growing mycobacteria. Antimicrob Agents Chemother. Mar 2001;45(3):764-7. [Medline].

  22. Wallace RJ, Brown-Elliott BA, Crist CJ, et al. Comparison of the in vitro activity of the glycylcycline tigecycline (formerly GAR-936) with those of tetracycline, minocycline, and doxycycline against isolates of nontuberculous mycobacteria. Antimicrob Agents Chemother. Oct 2002;46(10):3164-7. [Medline].

  23. Hyon JY, Joo MJ, Hose S, Sinha D, Dick JD, O'Brien TP. Comparative efficacy of topical gatifloxacin with ciprofloxacin, amikacin, and clarithromycin in the treatment of experimental Mycobacterium chelonae keratitis. Arch Ophthalmol. Aug 2004;122(8):1166-9. [Medline].

  24. Holland SM. Nontuberculous mycobacteria. Am J Med Sci. Jan 2001;321(1):49-55. [Medline].

  25. Griffith DE, Wallace RJ. New developments in the treatment of nontuberculous mycobacterial (NTM) disease. Semin Respir Infect. Dec 1996;11(4):301-10. [Medline].

  26. Iseman MD, Marras TK. The importance of nontuberculous mycobacterial lung disease. Am J Respir Crit Care Med. Nov 15 2008;178(10):999-1000. [Medline].

  27. Kim RD, Greenberg DE, Ehrmantraut ME, Guide SV, Ding L, Shea Y, et al. Pulmonary nontuberculous mycobacterial disease: prospective study of a distinct preexisting syndrome. Am J Respir Crit Care Med. Nov 15 2008;178(10):1066-74. [Medline].

  28. Kyle SD, Porter WM. Mycobacterium chelonae infection successfully treated with oral clarithromycin and linezolid. Br J Dermatol. Nov 2004;151(5):1101. [Medline].

  29. Mitchell JD, Bishop A, Cafaro A, Weyant MJ, Pomerantz M. Anatomic lung resection for nontuberculous mycobacterial disease. Ann Thorac Surg. Jun 2008;85(6):1887-92; discussion 1892-3. [Medline].

  30. Parrish SC, Myers J, Lazarus A. Nontuberculous mycobacterial pulmonary infections in Non-HIV patients. Postgrad Med. Nov 2008;120(4):78-86. [Medline].

  31. Tabarsi P, Baghaei P, Farnia P, Mansouri N, Chitsaz E, Sheikholeslam F, et al. Nontuberculous mycobacteria among patients who are suspected for multidrug-resistant tuberculosis-need for earlier identification of nontuberculosis mycobacteria. Am J Med Sci. Mar 2009;337(3):182-4. [Medline].

  32. U.S. Food and Drug Administration. Available at http://www.fda.gov/cder/drug/infopage/linezolid/default.htm.

  33. van Ingen J, Boeree MJ, de Lange WC, Dekhuijzen PN, van Soolingen D. Impact of new American Thoracic Society diagnostic criteria on management of nontuberculous mycobacterial infection. Am J Respir Crit Care Med. Aug 15 2007;176(4):418; author reply 419. [Medline].

  34. Wagner D, Young LS. Nontuberculous mycobacterial infections: a clinical review. Infection. Oct 2004;32(5):257-70. [Medline].

Keywords

Mycobacterium chelonei, M chelonei, M chelonae, Mycobacterium chelonae, Mycobacterium abscessus, M abscessus, nontuberculous mycobacterium, nontuberculous mycobacteria, mycobacterium other than tuberculosis, MOTT, Mycobacterium tuberculosis, mycobacterial cutaneous infection, NTM, NTM lung disease, AIDS, HIV, Runyon classification, Runyon's classification, Runyon classification group IV, Runyon group IV, rapidly growing mycobacteria, osteomyelitis, keratitis, corneal ulcers

Contributor Information and Disclosures

Author

F Matthew Kuhlmann, MD, Fellow, Division of Infectious Diseases, Washington University School of Medicine
F Matthew Kuhlmann, MD is a member of the following medical societies: American Medical Association and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

Coauthor(s)

Keith F Woeltje, MD, PhD, Associate Professor, Department of Internal Medicine, Division of Infectious Diseases, Washington University School of Medicine
Keith F Woeltje, MD, PhD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Medical Informatics Association, Infectious Diseases Society of America, and Society for Healthcare Epidemiology of America
Disclosure: Nothing to disclose.

Medical Editor

Klaus-Dieter Lessnau, MD, FCCP, Clinical Associate Professor of Medicine, New York University School of Medicine; Medical Director, Pulmonary Physiology Laboratory; Director of Research in Pulmonary Medicine, Department of Medicine, Section of Pulmonary Medicine, Lenox Hill Hospital
Klaus-Dieter Lessnau, MD, FCCP is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, American Medical Association, American Society for Artificial Internal Organs, American Thoracic Society, Physicians for Social Responsibility, and Society of Critical Care Medicine
Disclosure: sepracor Ownership interest None

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Aaron Glatt, MD, Professor of Clinical Medicine, New York Medical College; President and CEO, Former Chief Medical Officer, Departments of Medicine and Infectious Diseases, New Island Hospital
Aaron Glatt, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physician Executives, American College of Physicians, American College of Physicians-American Society of Internal Medicine, American Medical Association, American Society for Microbiology, American Thoracic Society, American Venereal Disease Association, Infectious Diseases Society of America, International AIDS Society, and Society for Healthcare Epidemiology of America
Disclosure: Nothing to disclose.

CME Editor

Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital
Eleftherios Mylonakis, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Society for Microbiology, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

Chief Editor

Burke A Cunha, MD, Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital
Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

 
 
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