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Dermatomyosite et cancer rectal: à propos d’un cas avec revue de la littérature

Dermatomyositis is a systemic idiopathic disease characterized by a combination of both muscle and skin symptoms. It is a paraneoplastic dermatosis. Its association with rectal cancer has been rarely described in the literature. We here report the case of a female patient with paraneoplastic dermato...

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Detalles Bibliográficos
Autores principales: Ouahbi, Hajar, Benhami, Meriem, Nouikh, Lamiae, Acharfi, Nissrine, Kelati, Awatef, Oualla, Karima, Benbrahim, Zineb, Elmrabet, Fatima Zahra, Arifi, Samia, Mernissi, Fatimazohra, Mellas, Nawfel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754859/
https://www.ncbi.nlm.nih.gov/pubmed/31558922
http://dx.doi.org/10.11604/pamj.2019.33.122.14509
Descripción
Sumario:Dermatomyositis is a systemic idiopathic disease characterized by a combination of both muscle and skin symptoms. It is a paraneoplastic dermatosis. Its association with rectal cancer has been rarely described in the literature. We here report the case of a female patient with paraneoplastic dermatomyositis associated with metastatic rectal adenocarcinoma presenting with clinical symptoms commonly found in subjects with paraneoplastic dermatomyositis. Other complementary examinations (CPK test + EMG + skin biopsy) were performed which confirmed this diagnosis. The patient underwent chemotherapy, but after the second cycle, she experienced a rapid worsening of her general condition and died after some days in a state of multisystem organ failure. This study aims to highlight paraneoplastic dermatomyositis’ aggressive nature and to update current knowledge on the importance of chemotherapy in the management of neoplastic dermatomyositis.