Meningomyeloencephalitis secondary to Mycobacterium haemophilum infection in AIDS

Sandra Leskinen1, Xena Flowers1, Katharina Thoene2

  • 1Department of Pathology & Cell Biology, Columbia University Irving Medical Center, New York, NY, 10032, USA.

Insights

Opportunistic non-tuberculous mycobacteria (NTM) infections are increasing. Mycobacterium haemophilum central nervous system (CNS) infection is rare but fatal, especially in AIDS patients, highlighting diagnostic challenges.

Area of Science:

  • Infectious Diseases
  • Neuropathology
  • Microbiology

Background:

  • Non-tuberculous mycobacteria (NTM) infections are globally increasing.
  • Mycobacterium haemophilum is an emerging NTM causing diverse infections, particularly in immunocompromised individuals.
  • Central nervous system (CNS) involvement by M. haemophilum is rarely reported, and diagnosis is challenging with conventional methods.

Observation:

  • A case of a 39-year-old man with AIDS who died from M. haemophilum CNS infection is presented.
  • The patient exhibited neurological symptoms, negative CSF cultures, and brainstem abnormalities on MRI.
  • Autopsy revealed significant neuropathologic findings, including lymphohistiocytic infiltrates, gliosis, neuronal loss, and acid-fast bacilli (AFB) in the CNS.

Findings:

  • The brainstem was the most severely affected area, with AFB concentrated along arterial territories, suggesting hematogenous spread.
  • Post-mortem 16S rRNA sequencing of formalin-fixed paraffin-embedded tissue successfully identified M. haemophilum.
  • This molecular technique offers a potential method for diagnosing M. haemophilum CNS infections from CSF samples.

Implications:

  • This case underscores the potential for M. haemophilum to cause severe CNS disease, even with negative initial workups.
  • Advanced molecular techniques like 16S rRNA sequencing are crucial for post-mortem identification and potentially for ante-mortem diagnosis.
  • Improved diagnostic strategies are needed to detect M. haemophilum CNS infections earlier, especially in immunocompromised populations.

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