Publication:
Azathioprine-induced alopecia: a rare adverse event, early marker of myelotoxicity.

dc.contributor.authorVázquez Rodríguez, Juan Antonio
dc.contributor.authorMerino Gallego, Esther
dc.contributor.authorBaños Arévalo, Antonio José
dc.contributor.authorGallardo Sánchez, Francisco
dc.contributor.authorMiras Lucas, Leticia
dc.contributor.authorPérez González, Álvaro
dc.date.accessioned2023-05-03T14:29:47Z
dc.date.available2023-05-03T14:29:47Z
dc.date.issued2022
dc.description.abstractThough not exempt from adverse events, azathioprine (AZA) is an inexpensive and effective drug in the induction and maintenance treatment of patients with inflammatory bowel disease. We present the case of a 20-year-old female patient with left-side ulcerative colitis in whom AZA was started at a dose of 1.5 mg/kg/day due to dependence on corticoids (thiopurine methyltransferase activity: 14.9 U/mL). Two weeks after starting treatment she began to report excessive hair loss, resulting in an almost complete loss of scalp hair.
dc.identifier.doi10.17235/reed.2021.8175/2021
dc.identifier.issn1130-0108
dc.identifier.pmid34517716
dc.identifier.unpaywallURLhttps://doi.org/10.17235/reed.2021.8175/2021
dc.identifier.urihttp://hdl.handle.net/10668/21713
dc.issue.number1
dc.journal.titleRevista espanola de enfermedades digestivas
dc.journal.titleabbreviationRev Esp Enferm Dig
dc.language.isoen
dc.organizationAPES Hospital de Poniente de Almería
dc.page.number63-64
dc.pubmedtypeCase Reports
dc.pubmedtypeJournal Article
dc.rights.accessRightsopen access
dc.subject.meshAdult
dc.subject.meshAlopecia
dc.subject.meshAzathioprine
dc.subject.meshBiomarkers
dc.subject.meshColitis, Ulcerative
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshImmunosuppressive Agents
dc.subject.meshInflammatory Bowel Diseases
dc.subject.meshMercaptopurine
dc.subject.meshMethyltransferases
dc.subject.meshYoung Adult
dc.titleAzathioprine-induced alopecia: a rare adverse event, early marker of myelotoxicity.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number114
dspace.entity.typePublication

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