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Methotrexate-induced toxidermia and pancytopenia in a patient with ectopic pregnancy: a case report

BACKGROUND: Methotrexate is an anticancer drug from the antimetabolite class. It is also used in gynecology and obstetrics and is the molecule of choice for the medical treatment of ectopic pregnancies. We report a case of toxidermia associated with severe pancytopenia induced by methotrexate for ec...

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Detalles Bibliográficos
Autores principales: Refeno, Valéry, Rasamimanana, Naharisoa Giannie, Abasse, Baco Abdallah, Ramarokoto, Malalafinaritra Patrick Marco, Fanomezantsoa, Mahefaniaina Jean Eustache, Randaoharison, Pierana Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650356/
https://www.ncbi.nlm.nih.gov/pubmed/34872594
http://dx.doi.org/10.1186/s13256-021-03111-x
Descripción
Sumario:BACKGROUND: Methotrexate is an anticancer drug from the antimetabolite class. It is also used in gynecology and obstetrics and is the molecule of choice for the medical treatment of ectopic pregnancies. We report a case of toxidermia associated with severe pancytopenia induced by methotrexate for ectopic pregnancy. CASE PRESENTATION: A 30-year-old Malagasy (African) woman was admitted to the Emergency and Intensive Care Department for probable toxidermia following injection of 75 mg of methotrexate for an ectopic pregnancy. She had developed generalized erythema, which started 48 hours after the injection. The secondary onset of phlyctenular maculopapular skin lesions, generalized purpura, and erosions of the oral mucosa in a context of febrile jaundice prompted her hospitalization. On admission, the patient presented with febrile neutropenia, pancytopenia, renal failure, and hepatic cytolysis. She received transfusions of fresh whole blood, erythromycin, and amphotericin B. The course was fatal within 2 days of hospitalization. The patient died of multiple organ failure. CONCLUSIONS: Our case is mainly distinguished by the lack of use of granulocyte growth factors and folinic acid. In the event of severe reactions to methotrexate, the management should be multidisciplinary and as much as possible within an intensive care unit.