Atypical Presentation of Isolated Cerebral Aspergillosis in a Renal Allograft Recipient
Published: July 1, 2017 | DOI: https://doi.org/10.7860/JCDR/2017/27919.10288
Minaxi H Patel, Aruna V Vanikar, Himanshu V Patel, Rashmi D Patel
1. Assistant Professor, Department of Pathology, Laboratory Medicine, Transfusion Services and Immunohematology, G.R. Doshi and K.M. Mehta Institute of Kidney
Diseases and Research Centre (IKDRC) - Dr. H.L. Trivedi, Ahmedabad, Gujarat, India.
2. Professor and Head, Department of Pathology, Laboratory Medicine, Transfusion Services and Immunohematology, G.R. Doshi and K.M. Mehta Institute of Kidney
Diseases and Research Centre (IKDRC) - Dr. H.L. Trivedi, Ahmedabad, Gujarat, India.
3. Professor, Department of Nephrology and Transplantation Medicine, G.R. Doshi and K.M. Mehta Institute of Kidney Diseases and Research Centre (IKDRC) - Dr. H.L.
Trivedi, Ahmedabad, Gujarat, India.
4. Professor, Department of Pathology, Laboratory Medicine, Transfusion Services and Immunohematology, G.R. Doshi and K.M. Mehta Institute of Kidney Diseases &
Research Centre (IKDRC) - Dr. H.L. Trivedi, Ahmedabad, Gujarat, India.
Correspondence
Dr. Aruna V Vanikar,
Professor and Head, Department of Pathology, Laboratory Medicine, Transfusion Services and Immunohematology and Department
of Cell Therapy and Regenerative Medicine, G.R. Doshi and K.M. Mehta Institute of Kidney Diseases, Ahmedabad, Gujarat, India.
E-mail: vanikararuna@yahoo.com
The immunosuppressive state in organ transplantation leads to infectious complications responsible for high mortality rate. Fungal infections account for 5% of all infections in Renal Transplantation (RT) recipients. Aspergillus species are filamentous fungi frequently causing fungal infections in RT recipients. Lungs and paranasal sinuses are the usual portal of entry from where it disseminates to other organs. Here, we are reporting a case of 14-year-old boy with RT from mother’s kidney, who had atypical presentation of isolated cerebral aspergillosis at 19 months post-transplant without identified portal of entry. Early diagnosis and prompt treatment saved the patient and the graft.
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