Hereditary spherocytosis concomitant with JAK2V617F-positive primary myelofibrosis: a case report

Hereditary spherocytosis (HS) is a genetic hemolytic disorder primarily characterized by hemolytic anemia, jaundice, splenomegaly, and frequent complications, including cholelithiasis, accompanied by the presence of spherocytes in the peripheral blood. This disorder predominantly follows an autosoma...

Full description

Bibliographic Details

Published in:	Frontiers in Oncology
Main Authors:	Chi-E Qiu, Lei Lei, Guosong Jiang, Xiuqun Huang, Yadan Li
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2025-10-01
Subjects:	hereditary spherocytosis primary myelofibrosis JAK2V617F comorbidity myeloproliferative neoplasm
Online Access:	https://www.frontiersin.org/articles/10.3389/fonc.2025.1665179/full