Multiple concurrent opportunistic infections in patient with myasthenia gravis: A case report

Jingrou Chen1,2, Jingchun Fang1,2, Li Sun3

  • 1Department of Laboratory Medicine, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Virulence
|August 28, 2025
PubMed

Insights

This case report details a myasthenia gravis patient experiencing severe gastrointestinal bleeding and multiple opportunistic infections after immunosuppressive therapy. Early detection and comprehensive management of these complex infections are crucial for patient outcomes.

Area of Science:

  • Clinical Medicine
  • Immunology
  • Infectious Diseases

Background:

  • Myasthenia gravis (MG) is a rare autoimmune disorder with a guarded prognosis, particularly when complicated by opportunistic infections.
  • Immunosuppressive therapy in MG patients increases the risk of severe and multiple infections, posing significant clinical challenges.

Purpose of the Study:

  • To analyze a clinical case of a middle-aged male patient with MG who developed severe lower gastrointestinal bleeding and multiple opportunistic infections post-immunosuppressive therapy.
  • To highlight the diagnostic and therapeutic complexities in managing co-existing infections in MG patients.

Main Methods:

  • Comprehensive clinical evaluations including colonoscopy, histopathology, bronchoscopy, bronchoalveolar lavage (BAL), and metagenomic next-generation sequencing (mNGS).
  • Histopathological examination confirmed Cytomegalovirus (CMV) and Histoplasmosis.
  • BAL fluid and mNGS identified infections with Aspergillus fumigatus, Talaromyces, Stenotrophomonas maltophilia, and Pneumocystis jirovecii.

Main Results:

  • The patient presented with persistent ptosis, pulmonary infection, and severe lower gastrointestinal bleeding.
  • Multiple pathogens including CMV, Histoplasmosis, Aspergillus, Talaromyces, S. maltophilia, and P. jirovecii were identified.
  • Treatment required adjustment to broad-spectrum anti-infectives and supportive care, including immunoglobulins and albumin.

Conclusions:

  • MG patients on immunosuppressive therapy require vigilant monitoring for opportunistic infections.
  • Simultaneous management of multiple pathogens in MG is complex and necessitates a multi-faceted approach.
  • Prompt and accurate diagnosis using advanced techniques like mNGS is vital for effective treatment strategies.

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