Dear Editor,
Non-tuberculous (atypical) mycobacteria are acid-mycolic-based bacteria that may cause various diseases of dermatological interest, such as skin and soft tissue infections. Their diagnosis is usually addressed by a thorough anamnesis, and clinical aspect, and confirmed by PCR exams when available.[1]
Here we present a case of an otherwise healthy 45 years old female patient who accessed our service after the appearance of strange and tender neoformations on her left, causing a stingy-painful sensation.
After a careful anamnestic interview, she said she experienced intensive gardening in her country house and installed a new aquarium the previous week.
Her past medical history is silent, and she has not taken drugs in a chronic or discontinuous manner in the last two months.
At physical examination, we appreciated some nodules and bullous formations on her medium finger, carpal end wrist end, and no axillary lymph nodes were appreciated on palpation.
We suspected infection with a sporotrichosis growth and requested a wide emathochimical panel. We executed a soft-tissue biopsy, a cultural sample for anaerobic and aerobic bacteria, fungi and PCR for sporothrix schenckii, mycobacterium, and leishmania complex (the country house of the patient was in an endemic area).
All the exams were negative, but since sporotrichosis infection seemed the more probable (due to timing, clinical history, and solid consistency of the lesions), we administered itraconazole 200 mg/die.[2]
Two weeks later patient condition worsened, and he was admitted to the hospital ward for further testing.
Among the other exams, we performed another PCR on fresh biopsy for mycobacterium complex, blood tests, CT lung scan, and abdomen ultrasound, all negatives.
At clinical observation, the cutaneous lesions were mainly of a bullous aspect, with a soft-liquid consistency [Figure 1a and b]. Some lymph node swelling was appreciated on the ipsilateral axilla.
An ultrasound exam of the most representative lesion of the hand highlighted the presence of a well-demarcated dermal formation, with liquid consistency on the upper part and a more echogenic content on the lower portion of the neoformed space. The lesion was enclosed by the epidermis and papillar dermis on the roof and hypoderma and fascial structures on the floor [Figure 2a]. Color-doppler examination showed enhanced vascular flux on the cavities’ basal side, suggesting an extended tissue inflammation [Figure 2b].
Tissue colliquation, among with local inflammation, a sporotrichosis dissemination, and regional lymph node swelling, was highly suggestive of mycobacterial infection.[3] But the now available cultural exams and the new PCR testing requested were negative for every microbiological affection.
Despite the double negative testing, we stopped itraconazole treatment and started rifampicin 10 mg/kg/day plus clarithromycin 15 mg/kg/day.
Lesions almost completely healed three weeks later, confirming the ex juvantibus diagnosis of atypical mycobacterial infection.[1]
Signs and medical history can indicate a nontuberculous mycobacterial infection, especially a history of water exposure, penetrating injury, surgical procedure, negative routine bacterial cultures, and lack of response to non-tubercular specific antibiotics.[4]
Although rarely, PCR can give false-negative results, empirical therapy was necessary in our case, providing an ex-adjuvantibus diagnosis.
Even if ultrasonography is not available in all dermatological divisions, it had an incisive role in this case: it demonstrated the presence of well-delimited nodules, exudate, and necrotic material indicative of an inflammatory process typical of tuberculous infections,[5,6,7] allowing consequently to establish the correct therapy.
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Conflicts of interest
There are no conflicts of interest.
References
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