Author ORCID Identifier
https://orcid.org/my-orcid?orcid=0000-0001-7421-2418
Abstract
Azathioprine is a pro-drug and is metabolized by the TPMT enzyme in the body. In South Asians, Azathioprine is known to cause alopecia and bone marrow suppression in patients with TPMT enzyme deficiency. In India, the prevalence of TPMT mutation varies from 1.2- 10%. A new mutation was detected in 2014, NUDT15 whose incidence varies from 8.5-16%. Patients with mutation in both TPMT and NUDT15 develop myelosuppression faster. In our case, alopecia manifested as the first clinical feature of Azathioprine myelosuppression. Physicians need to recognize early clinical clues (alopecia) to avoid the impending development of myelosuppression and to look for possible gene mutations.
Publication Date
2024
Publisher
JSS Academy of Higher Education and Research
Conflict of Interest
None
Keywords
Azathioprine, Alopecia, Myelosuppression, NUDT15, TPMT
Word Count
974
Recommended Citation
Dutta N , Final Year MBBS, Babu D , Professor, Ramaswamy D , Professor, Mamadapur D , Assistant Professor.
Alopecia as an Early Clinical Marker for Azathioprine Induced Myelosuppression: A Case Report.
Digital Journal of Clinical Medicine.
2024;
6(1):
-.
doi:
https://doi.org/10.55691/2582-3868.1173
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