Microsporidial myositis, keratitis and hypercalcaemia in a cystic fibrosis lung transplant recipient.
Anna Louise WatsonMarko MaticThomas RobertsonAlexandra Gabrielle Ann StewartPublished in: BMJ case reports (2022)
A man in his 50s was admitted with 4 months of myalgia, headaches, hypercalcaemia and declining renal function on a background of lung transplantation for cystic fibrosis 5 years prior. MRI confirmed myositis and a muscle biopsy revealed invasive muscular microsporidial infection. Positron emission tomography(PET)/CT revealed widespread dissemination of the infection. Albendazole was commenced and after a 1 week systemic inflammatory response syndrome, the patient made a significant recovery and was discharged home. PCR testing confirmed the species as Anncaliia algerae , which is known to infect mosquitoes, larvae and contaminate water supplies. This case highlights the need to relentlessly pursue a diagnosis and to consider atypical pathology in immune compromised patients. A tissue sample yielded highly beneficial and unexpected results. A multispecialty approach was essential given the varied infection manifestations, which included myositis, keratitis and possible central nervous system, vocal cord, parapharyngeal and renal involvement.
Keyphrases
- positron emission tomography
- pet ct
- cystic fibrosis
- computed tomography
- inflammatory response
- end stage renal disease
- interstitial lung disease
- pseudomonas aeruginosa
- case report
- newly diagnosed
- ejection fraction
- chronic kidney disease
- single cell
- magnetic resonance imaging
- lung function
- aedes aegypti
- skeletal muscle
- systemic sclerosis
- lps induced
- peritoneal dialysis
- lipopolysaccharide induced
- body composition
- immune response
- genetic diversity
- toll like receptor
- idiopathic pulmonary fibrosis
- zika virus
- patient reported
- air pollution
- high intensity