Oral and Cervicofacial Infection Secondary to Agranulocytosis Caused by Antithyroid Medication: A Case Report

Descripción del Articulo

Agranulocytosis refers to a low white blood cell count, specifically neutrophils, which can be caused by certain medications such as antithyroid drugs (ATD). This condition can result in oral manifestations, including diffuse gingival ulceration or necrosis. We present the case of a 26-year-old fema...

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Detalles Bibliográficos
Autores: Paredes Vilchez, Renzo Angel, Concha Cusihuallpa, Hiroshi, Carrión Gamarra, Henry, Arteaga Ramirez, Katherine, Santiago Valverde, Juver Edinson, Campos Valenzuela, Omar, Gonzales Takano, Kenyi Koichi
Formato: artículo
Fecha de Publicación:2023
Institución:Universidad Peruana Cayetano Heredia
Repositorio:Revistas - Universidad Peruana Cayetano Heredia
Lenguaje:español
OAI Identifier:oai:revistas.upch.edu.pe:article/4514
Enlace del recurso:https://revistas.upch.edu.pe/index.php/REH/article/view/4514
Nivel de acceso:acceso abierto
Materia:agranulocitosis
hipertiroidismo
úlcera necrotizante
metimazol
agranulocytosis
hyperthyroidism
necrotizing ulcer
methimazole
Descripción
Sumario:Agranulocytosis refers to a low white blood cell count, specifically neutrophils, which can be caused by certain medications such as antithyroid drugs (ATD). This condition can result in oral manifestations, including diffuse gingival ulceration or necrosis. We present the case of a 26-year-old female patient with a history of hyperthyroidism who came to the emergency department of Alberto Sabogal Sologuren National Hospital with swelling on the left side of her face, accompanied by dysphagia, multiple ulcerated lesions in the oral mucosa involving bone tissue, as well as fever and general malaise. After conducting additional tests, the patient was diagnosed with oral and cervicofacial infection secondary to agranulocytosis caused by methimazole treatment. While the global literature reports cases of agranulocytosis as an adverse effect of antithyroid medication, with documented oral manifestations, only a few cases demonstrate cervical involvement. Therefore, we present this uncommon case from diagnosis to treatment.
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