International Journal of Infectious Diseases (Jun 2021)
Invasive cerebral phaeohyphomycosis in a Chinese boy with CARD9 deficiency and showing unique radiological features, managed with surgical excision and antifungal treatment
- Sophie H.Y. Lai,
- Jaime S. Rosa Duque,
- Brian Hon-Yin Chung,
- Tom Wai-Hin Chung,
- Daniel Leung,
- Ronnie Siu-Lun Ho,
- Raymand Lee,
- Rosana W.S. Poon,
- Gilbert T. Chua,
- Kai-Ning Cheong,
- Martin Man Chun Chui,
- Mianne Lee,
- Sidney Tam,
- Andrew Ho Cheuk Him,
- King-Fai Cheng,
- Wilson Wai-Shing Ho,
- Kwok-Yung Yuen,
- Pamela Lee,
- Yu-Lung Lau
Affiliations
- Sophie H.Y. Lai
- Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong
- Jaime S. Rosa Duque
- Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong; Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Brian Hon-Yin Chung
- Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Tom Wai-Hin Chung
- Department of Microbiology, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Daniel Leung
- Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Ronnie Siu-Lun Ho
- Department of Pathology, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Raymand Lee
- Department of Radiology, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Rosana W.S. Poon
- Department of Microbiology, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Gilbert T. Chua
- Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong; Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Kai-Ning Cheong
- Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong; Hong Kong Children’s Hospital, Hong Kong
- Martin Man Chun Chui
- Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Mianne Lee
- Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Sidney Tam
- Department of Pathology, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Andrew Ho Cheuk Him
- Department of Neurosurgery, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- King-Fai Cheng
- Department of Neurosurgery, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Wilson Wai-Shing Ho
- Department of Neurosurgery, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Kwok-Yung Yuen
- Department of Microbiology, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
- Pamela Lee
- Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong; Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong; Hong Kong Children’s Hospital, Hong Kong
- Yu-Lung Lau
- Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong; Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong; Hong Kong Children’s Hospital, Hong Kong; Corresponding author at: Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Room 106, 1/F, New Clinical Building, 102 Pokfulam Road, Queen Mary Hospital, Hong Kong.
- Journal volume & issue
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Vol. 107
pp. 59 – 61
Abstract
We report this rare case of cerebral phaeohyphomycosis in a previously healthy Chinese boy, who was found to have caspase recruitment domain family member 9 (CARD9) deficiency. Initial radiological features suggested a neoplastic cerebral lesion, while histopathological examination supplemented by internal transcribed sequencing (ITS) of cerebral tissue confirmed the diagnosis of phaeohyphomycosis. He was treated with intravenous (IV) liposomal amphotericin B and voriconazole, guided by plasma and cerebrospinal fluid (CSF) level monitoring at drug initiation. At the 1 year follow-up, the patient demonstrated near complete neurological and radiological recovery.