Literature DB >> 34912746

Mycobacterium chelonae Cutaneous Infection: A Challenge for an Internist.

Margarida Gaudêncio1, André Carvalho1, Maria Inês Bertão1, Ivo Barreiro1, Maria Isabel Bessa1, Abílio Gonçalves1.   

Abstract

Cutaneous infections caused by the Mycobacterium chelonae complex show a heterogeneous clinical presentation, which varies according to the patient's immune status. Most standard antimycobacterials have no effect against these species. Clarithromycin alone was shown to provide adequate treatment, although resistance has been reported. Consequently, the literature supports multi-drug therapy to combat resistant strains. Here, we describe the case of a 59-year-old man under systemic immunosuppressive therapy who developed cutaneous lesions whose evolution was highly suggestive of atypical infection. LEARNING POINTS: Mycobacterium chelonae is a ubiquitous species of mycobacteria found in the environment; cutaneous infections by the M. chelonae complex show a heterogeneous clinical presentation.The combination of linezolid and clarithromycin has been used in some cases, with rapid clinical resolution and less or no relapse observed after long-term follow-up.Internal Medicine is the appropriate speciality to treat particularly complex or multisystem diseases, such as infections in immunocompromised patients. © EFIM 2021.

Entities:  

Keywords:  Mycobacterium chelonae; atypical specimens; cutaneous infection; immunosuppression

Year:  2021        PMID: 34912746      PMCID: PMC8668006          DOI: 10.12890/2021_003013

Source DB:  PubMed          Journal:  Eur J Case Rep Intern Med        ISSN: 2284-2594


INTRODUCTION

Mycobacterium chelonae is a non-tuberculous, rapidly growing species of mycobacteria that is often grouped together with Mycobacterium fortuitum and abscessus due to their similar clinical and metabolic features [. It is found in soil, dust and natural water supplies [. Infection typically follows incidental environmental inoculation [. The cutaneous manifestations vary according to the patient’s immune status [. Localized infections such as cellulitis and abscesses are commonly seen in immunocompetent patients, while disseminated skin disease occurs in immunosuppressed patients (organ transplantation, chemotherapy, autoimmune disorders, long-term steroid therapy or biologic therapies) [. In disseminated disease, the limbs are predominantly involved and show different types of lesions such as pustules, nodules, abscesses or ulcers, commonly with a sporotrichoid pattern [. Other less common presentations reported in the literature include osteomyelitis, pneumonitis, lymphadenitis, corneal ulcers, endocarditis and catheter-related infections [. Histopathological findings are non-specific and tend to include a granulomatous inflammatory cell infiltrate with abundant neutrophils [. Dermal or subcutaneous abscesses, acute or chronic panniculitis or a non-specific chronic inflammation can be found [. The authors describe a very unusual case of M. chelonae infection with severe cutaneous involvement after long-term immunosuppressive therapy.

CASE DESCRIPTION

A 59-year-old man diagnosed with sarcoidosis in 1978 was under systemic immunosuppressive therapy with azathioprine 100 mg/day and methylprednisolone 8 mg/day. He also had a history of chronic obstructive pulmonary disease, a pulmonary embolism in 2019 (negative study for thrombophilia and antiphospholipid syndrome), obstructive sleep apnoea and respiratory failure requiring nocturnal non-invasive ventilation and daytime oxygen therapy. The patient did not have any tattoos. The patient presented a 2-week history of multiple painful, erythematous nodules distributed over the posterior right arm (Fig. 1A). Cutaneous biopsy showed abscess formation and no granulomatous infiltrate.
Figure 1

Upper panel. Evolution of skin lesions. (A) The first skin lesions appeared as multiple, painful erythematous nodules distributed only over the posterior right arm. (B) After 3 months of therapy with trimethoprim/sulfamethoxazole, the skin lesions had increased and were distributed over the limbs, face, trunk and abdomen.

Lower panel. Evolution of skin lesions - continuation. (C) Erythematous papules and nodules, pustular lesions and haemorrhagic crusts distributed over limbs during hospitalization. (D) Progressive improvement in skin lesions after 9 months of therapy

The first cultures identified Turicella otitidis and the patient started cefuroxime. However, he did not show any improvement and so cultures were repeated, revealing the presence of Nocardia and Actinomyces. After 3 months of therapy with trimethoprim/sulfamethoxazole, the patient developed more skin lesions (erythematous papules and nodules, pustular lesions and haemorrhagic crusts) distributed over the limbs, face, trunk and abdomen (Fig. 1B). About 2–3 months after the first appearance of the skin lesions, the patient experienced sporadic episodes of rectal bleeding. A study of the digestive tract was requested, but the patient postponed investigation. However, he experienced frequent episodes of rectal bleeding and anaemia (haemoglobin 12.3–12.7 g/dl) associated with weight loss (10 kg in 1 month). So, 5 months after symptom onset, an endoscopy and colonoscopy were performed. Thoraco-abdominopelvic tomography showed known diffuse emphysematous changes in pulmonary parenchyma and several calcified hilar and mediastinal ganglion cysts, as well as absence of metastasis. Rectal adenocarcinoma was diagnosed and the patient was submitted to radiotherapy before abdominoperineal resection. The patient was later hospitalized due to a cytomegalovirus infection and for intravenous antibiotics (Fig. 1C). Skin cultures were repeated and research laboratory support was requested for molecular analysis, which revealed M. chelonae (susceptible to amikacin, ciprofloxacin, linezolid and clarithromycin). The patient started a 12-month linezolid and clarithromycin regimen. Currently, he has complete 9 months of therapy with progressive improvement in skin lesions (Fig. 1D).

DISCUSSION

Skin, bone and soft tissue diseases are the most frequent clinical manifestations of M. chelonae infection [. Our case is notable due to the numerous pustules, nodules, abscesses and haemorrhagic crusts distributed over the limbs, face, trunk and abdomen, showing a sporotrichoid pattern. Skin infections have been reported following surgery, acupuncture, mesotherapy and tattooing [. In the case of tattoos, the infections affect areas coloured grey, as non-sterile water is added to black ink [8]. In this case, the patient did not have any tattoos, so inoculation of this agent may have occurred during contact with soil and exotic plants. The fact that the patient was immunosuppressed also contributed to infection. Most standard antimycobacterials such as ethambutol, pyrazinamide and isoniazid, have no effect against these species [. Clarithromycin alone was shown to provide adequate treatment, although resistance has been reported [. Resistance to other antimicrobials such as erythromycin, ciprofloxacin, ofloxacin and sulfamethoxazole, has also been described [. The literature supports multi-drug therapy to avoid selecting resistant strains and a prolonged therapy period in order to prevent relapse [. Treatment for this type of infection has not yet been standardized [. Guidelines published by the American Thoracic Society on non-tuberculous mycobacterial diseases in 2007 recommend a minimum of 4–6 months of treatment with combination antibiotic therapy for cutaneous infections [. However, there are differences between treatment for immunocompetent and immunocompromised patients [. We report this case because of its striking and unusual clinical presentation, which provides a good example of the role of immunosuppression as a major risk factor for non-tuberculous mycobacterial infection. This case also highlights the importance of treating these types of cases with an extended course of appropriate antibiotics, particularly in immunocompromised patients. Furthermore, there is clearly a need for treatment guidelines for M. chelonae cutaneous infections. In conclusion, with this case, the authors hope to alert physicians to consider M. chelonae infection in cases of intractable skin lesions and to collect specimens and culture pathogens, repeatedly if necessary, as we did. We isolated different atypical agents at an early stage, but due to the lack of therapeutic response, continued our search until we identified the species responsible.
  12 in total

1.  Disseminated cutaneous Mycobacterium chelonae infection.

Authors:  C L Kane; A L Vincent; J N Greene; R L Sandin
Journal:  Cancer Control       Date:  2000 Mar-Apr       Impact factor: 3.302

2.  Atypical mycobacterial cutaneous infection.

Authors:  P Kullavanijaya
Journal:  Clin Dermatol       Date:  1999 Mar-Apr       Impact factor: 3.541

3.  [Facial lesions after tattooing].

Authors:  A Lapresta; C Pérez; D García-Almagro
Journal:  Actas Dermosifiliogr       Date:  2010-12

4.  Disseminated cutaneous Mycobacterium chelonae infection in an immunocompetent host.

Authors:  J Halpern; A Biswas; A Cadwgan; B B Tan
Journal:  Clin Exp Dermatol       Date:  2010-04       Impact factor: 3.470

Review 5.  An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases.

Authors:  David E Griffith; Timothy Aksamit; Barbara A Brown-Elliott; Antonino Catanzaro; Charles Daley; Fred Gordin; Steven M Holland; Robert Horsburgh; Gwen Huitt; Michael F Iademarco; Michael Iseman; Kenneth Olivier; Stephen Ruoss; C Fordham von Reyn; Richard J Wallace; Kevin Winthrop
Journal:  Am J Respir Crit Care Med       Date:  2007-02-15       Impact factor: 21.405

6.  Cutaneous Mycobacterium chelonae infection presenting as symmetrical plaques on both shins in an immunocompetent patient.

Authors:  Woon-Kyong Chung; Myoung-Shin Kim; Chae-Hwa Kim; Mi-Woo Lee; Jee-Ho Choi; Kee-Chan Moon; Jai-Kyoung Koh
Journal:  Acta Derm Venereol       Date:  2009-11       Impact factor: 4.437

Review 7.  Cutaneous infections due to nontuberculous mycobacteria: histopathological review of 28 cases. Comparative study between lesions observed in immunosuppressed patients and normal hosts.

Authors:  R Bartralot; R M Pujol; V García-Patos; D Sitjas; N Martín-Casabona; P Coll; A Alomar; A Castells
Journal:  J Cutan Pathol       Date:  2000-03       Impact factor: 1.587

8.  Skin, soft tissue, and bone infections due to Mycobacterium chelonae chelonae: importance of prior corticosteroid therapy, frequency of disseminated infections, and resistance to oral antimicrobials other than clarithromycin.

Authors:  R J Wallace; B A Brown; G O Onyi
Journal:  J Infect Dis       Date:  1992-08       Impact factor: 5.226

9.  Disseminated cutaneous Mycobacterium chelonae infection with multidrug resistance in a patient with panuveitis.

Authors:  K Phillips; S Blackford; N Berry
Journal:  Clin Exp Dermatol       Date:  2007-11-15       Impact factor: 3.470

10.  Disseminated Mycobacterium chelonae cutaneous infection: recalcitrant to combined antibiotic therapy.

Authors:  Preya Kullavanijaya; Niramol Rattana-Apiromyakij; Palachart Sukonthapirom-Napattalung; Supreeya Sirimachand; Imelda Duangdeeden
Journal:  J Dermatol       Date:  2003-06       Impact factor: 4.005

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