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Disseminated folliculitis by Mycobacterium fortuitum in an immunocompetent woman*

Foliculite disseminada causada por Mycobacterium fortuitum em mulher imunocompetente

Abstracts

Mycobacterium fortuitum is a non-tuberculous fast-growing mycobacterium which is frequently acquired from environmental sources such as soil and water. Since it is an opportunist pathogen, it is associated with trauma, surgery or immunodeficiency. The current report describes a case of Mycobacterium fortuitum-caused disseminated lesions on the skin of an immunocompetent patient.

Folliculitis; Nontuberculous Mycobacteria; Mycobacterium fortuitum


Mycobacterium fortuitum é uma micobactéria não tuberculosa de rápido crescimento, freqüentemente adquirida em fontes ambientais como solo e água. E um patógeno oportunista que está geralmente associado a trauma, procedimentos cirúrgicos, ou imunodeficiência. Este relato descreve um caso de lesões disseminadas na pele causada por Mycobacterium fortuitum em paciente sem imunocomprometimento.

Foliculite; Micobactérias não tuberculosas; Mycobacterium fortuitum


INTRODUCTION

There are currently over 140 species of nontuberculous mycobacteria (NTM) and that number has been increasing every year. NTM is a widely diverse group of organisms with a broad spectrum of virulence and potential to cause human disease.11. Alvarez-Uria G. Lung disease caused by nontuberculous mycobacteria. Curr Opin Pulm Med. 2010;16:251-6. Diseases caused by NTM, which have been grouped as mycobacterioses, show a wide broad spectrum of clinical manifestations and are not usually transmitted from man to man.22. American Thoracic Society. Diagnosis and treatment of disease caused by nontuberculous mycobacteria. Am Rev Respir Dis. 1990;142:940-53. Cutaneous mycobacterioses are not common; clinical, histopathological and bacteriological findings are not very distinct, making the diagnosis difficult.33. Oliveira e Sousa ACG, Pereira CP, Guimarães NS, Rego VR, Barbosa Jr. AA. Micobacteriose Cutânea Atípica pós-mesoterapia. An Bras Dermatol. 2001;76:711-5.

Mycobacterium fortuitum is a rapidly growing NTM, often acquired from environmental sources such as soil and water. It is considered an opportunistic pathogen often associated with trauma, surgical procedures, or immunodeficiency.44. Chen HY, Chen CY, Huang, CT, Ruan SY, Chou CH, Lai CC, et al. Skin and soft-tissue infection caused by non-tuberculous mycobacteria in Taiwan, 1997-2008. Epidemiol Infect. 2011;139:121-9.,55. Serra C, Loi G, Saddi B, Pautasso M, Manzin A. Unusual Clinical Presentation of Mycobacterium fortuitum Infection in an Immunocompetent Woman. J Clin Microbiol. 2007;45:1663-5. There are few reports of infections in healthy hosts, which include cutaneous and soft tissue after intramuscular injections, breast augmentation and other forms of surgery, soft tissue infection following acupunture and also outbreaks of M. fortuitum as agents of furunculosis on the legs after pedicure procedures.55. Serra C, Loi G, Saddi B, Pautasso M, Manzin A. Unusual Clinical Presentation of Mycobacterium fortuitum Infection in an Immunocompetent Woman. J Clin Microbiol. 2007;45:1663-5.,66. Guevara-Patiño A, Sandoval de Mora M, Farreras A, Rivera-Olivero I, Fermin D, de Waard JH. Soft tissue infection due to Mycobacterium fortuitum following acupuncture: a case report and review of the literature. J Infect Dev Ctries. 2010;4:521-5.,77. Vugia DJ, Jang Y, Zizeh C, Ely E, Winthrop KL, Desmond E. Mycobacteria in nail salon whirlpool footbaths, California. Emerg Infect Dis. 2005;11:616-8. The pathogenicity of M. fortuitum is unclear but it is known that local trauma is the most important entry point for infections of the skin and soft tissues, followed by nosocomial acquisition.88. Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial disease. Am J Respir Crit Care Med. 2007;175:367-416.

NTM infection should be considered in the differential diagnosis of chronic infection, fever of unknown origin and localized disease (abscesses, ulcers, nodules, infiltration, etc.) that do not respond to antibiotics commonly used in skin infections.66. Guevara-Patiño A, Sandoval de Mora M, Farreras A, Rivera-Olivero I, Fermin D, de Waard JH. Soft tissue infection due to Mycobacterium fortuitum following acupuncture: a case report and review of the literature. J Infect Dev Ctries. 2010;4:521-5.This report describes a case of disseminated skin lesions caused by M. fortuitum in an young woman without clinical signs of immunosuppression.

CASE REPORT

A 32-year-old woman who worked as a nurse in hospitals in Maringá, Parana, Brazil, suffered from erythema nodule-type lesions with some cold abscesses. The lesions had diameters ranging from 5 to 30 mm, on the trunk and on the upper and lower members, with an evolution of approximately 60 days (Figure 1). At first, the patient was treated with cephalexin 500 mg four times daily, for furunculosis, and later, with ciprofloxacin 500 mg orally twice daily for 14 days, with no improvement. Puncture and drainage of certain lesions were undertaken and specimens submitted to culture. Results were negative for aerobic bacteria and facultative anaerobic ones. The patient was then treated with rifampicin 600 mg orally twice daily and tetracycline 500 mg, four times daily, for 30 days, without any clinical improvement. The patient underwent biopsy for pathological test and culture for Acid-Fast Bacilli (AFB), fungi and pyogenic bacteria. Complementary tests, such as hemoculture, Hemogram, Aspartate Aminotranspherase (AST), Alanine-aminotranspherase (ALT), Urea, Createnin, Hemosedimentation speed, Antinuclear Antibodies (ANA), serology for HIV, Hepatitis C and B (HBs Ag, Anti-HBc, Anti-HBs), acid Alpha 1-glycoprotein, Immunoglobulins (IgE, IgA, IgG, IgM), Rheumatoid factor, Reactive Protein "C", Complement C3 and C4, CD4/CD8, were performed. The pathological test indicated deep perforating and suppurating folliculitis surrounded by a granulomatous and suppurating inflammatory process typifying a foreign body, coupled to a superficial and perivascular limphohistoplasmocytarian infiltrate and to a deep periadnexal infiltrate. Direct research for fungi and AFB showed negative results. Culture for AFB was positive in less than seven days at 30ºC and 35ºC. No growth of other bacteria occurred. Identification of AFB isolate was undertaken by Restriction Fragment Length Polymorphism Analysis (PCR-PRA) as Mycobacterium fortuitum complex.99. Telenti A, Marchesi F, Balz M, Bally F, Böttger EC, Bodmer T. Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis. J Clin Microbiol. 1993;31:175-8.No complementary test produced any changes that would justify involvement of other infectious pathogens. The patient underwent treatment using intravenous amikacin 1 g, three times weekly, clarithromycin 500 mg orally twice daily, during 12 weeks. Afterward monotherapy was maintained with clarithromycin 500 mg twice daily for 12 months. The elapsed time from first medical appointment until the beginning of therapy that achieved regression of lesions was approximately two months. By the end of treatment the patient experienced total regression of skin lesions with no recurring factor up to the present.

FIGURE 1
A. Erythematous nodular lesions on the trunk; B,C,D erythematous nodular lesions on lower members of the body

DISCUSSION

The current report describes a case of M. fortuitum-caused disseminated skin lesions in patient without clinical signs of immunosuppression. This is different from cases with localized lesions currently described in the literature.1010. Sethi S, Sharma M, Ray P, Singh M, Gupta A. Mycobacterium fortuitum wound infection following laparoscopy. Indian J Med Res. 2001;113: 83-4. Since the patient did not have either a surgical history or any other type of skin trauma, the source of M. fortuitum infection remained unknown.

M. fortuitum is frequently sensitive in vitro to several oral antimicrobial agents, including last generation quinolone, macrolides, doxycyclines, minocyclines, amikacin and sulfonamide.1111. Swenson JM, Wallace RJJr, Silcox VA, Thornsberry C. Antimicrobial susceptibility testing of 5 subgroups of Mycobacterium fortuitum and Mycobacterium chelonae. Antimicrob Agents Chemother. 1985;28: 807-11. With the therapy initially employed, the patient demonstrated bacterial resistance to ciprofloxacin. However, when the infectious agent was identified as belonging to the genus Mycobacterium spp. and therapy with amikacin and clarithromycin started, the patient showed complete resolution of lesions. In spite of the fact that 80% of isolates are sensitive to clarithromycin, experts do not recommend monotherapy and justify the association with amikacin.88. Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial disease. Am J Respir Crit Care Med. 2007;175:367-416.Recent studies have shown that a significant amount of M. fortuitum are resistant to macrolides and that, as a rule, antimicrobial resistance in M. fortuitum may not be detected by routine sensitivity tests.88. Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial disease. Am J Respir Crit Care Med. 2007;175:367-416.For a high cure probability, a minimum therapy period of four months is recommended in bone, serious cutaneous and soft tissues infections using at least two active agents.88. Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial disease. Am J Respir Crit Care Med. 2007;175:367-416.

Current report highlights the need to include M. fortuitum in the differential diagnosis of cutaneous infections that fail to respond to antimicrobial therapy against pyogenic bacteria. This is due to the fact that non-tuberculous mycobacteria have been isolated with greater frequency. The issue requiring an answer in situations described above is whether such increase occurred through the improvement of diagnosis techniques or through an increase in mycobacterial virulence.

REFERENCES

  • 1
    Alvarez-Uria G. Lung disease caused by nontuberculous mycobacteria. Curr Opin Pulm Med. 2010;16:251-6.
  • 2
    American Thoracic Society. Diagnosis and treatment of disease caused by nontuberculous mycobacteria. Am Rev Respir Dis. 1990;142:940-53.
  • 3
    Oliveira e Sousa ACG, Pereira CP, Guimarães NS, Rego VR, Barbosa Jr. AA. Micobacteriose Cutânea Atípica pós-mesoterapia. An Bras Dermatol. 2001;76:711-5.
  • 4
    Chen HY, Chen CY, Huang, CT, Ruan SY, Chou CH, Lai CC, et al. Skin and soft-tissue infection caused by non-tuberculous mycobacteria in Taiwan, 1997-2008. Epidemiol Infect. 2011;139:121-9.
  • 5
    Serra C, Loi G, Saddi B, Pautasso M, Manzin A. Unusual Clinical Presentation of Mycobacterium fortuitum Infection in an Immunocompetent Woman. J Clin Microbiol. 2007;45:1663-5.
  • 6
    Guevara-Patiño A, Sandoval de Mora M, Farreras A, Rivera-Olivero I, Fermin D, de Waard JH. Soft tissue infection due to Mycobacterium fortuitum following acupuncture: a case report and review of the literature. J Infect Dev Ctries. 2010;4:521-5.
  • 7
    Vugia DJ, Jang Y, Zizeh C, Ely E, Winthrop KL, Desmond E. Mycobacteria in nail salon whirlpool footbaths, California. Emerg Infect Dis. 2005;11:616-8.
  • 8
    Griffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial disease. Am J Respir Crit Care Med. 2007;175:367-416.
  • 9
    Telenti A, Marchesi F, Balz M, Bally F, Böttger EC, Bodmer T. Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis. J Clin Microbiol. 1993;31:175-8.
  • 10
    Sethi S, Sharma M, Ray P, Singh M, Gupta A. Mycobacterium fortuitum wound infection following laparoscopy. Indian J Med Res. 2001;113: 83-4.
  • 11
    Swenson JM, Wallace RJJr, Silcox VA, Thornsberry C. Antimicrobial susceptibility testing of 5 subgroups of Mycobacterium fortuitum and Mycobacterium chelonae. Antimicrob Agents Chemother. 1985;28: 807-11.
  • * Study carried out at the Clinical Bacteriology Laboratory-LEPAC of the Department of Clinical Analyses and Biomedicine, (Universidade Estadual de Maringá-UEM) - Maringá (PR), Brazil.

Publication Dates

  • Publication in this collection
    Feb 2013

History

  • Received
    23 Sept 2011
  • Accepted
    29 Dec 2011
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