Development of myelofibrosis and acute monocytic leukemia in a patient with hereditary spherocytosis: A case report

INTRODUCTION: Common symptoms of hereditary spherocytosis (HS) include intermittent jaundice and splenomegaly. Here, we present an unusual clinical course wherein a patient with HS treated with splenectomy developed secondary myelofibrosis and acute monocytic leukemia (M5). PATIENT CONCERNS: After p...

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Detalles Bibliográficos
Autores principales: Qian, Juan, Shen, Qian, Yin, Hong, Shi, Wen-yu, Yang, Li, Zhang, Ya-ping, Liu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
5700
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6922592/
https://www.ncbi.nlm.nih.gov/pubmed/31852097
http://dx.doi.org/10.1097/MD.0000000000018266

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6922592/
https://www.ncbi.nlm.nih.gov/pubmed/31852097
http://dx.doi.org/10.1097/MD.0000000000018266

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