期刊： JOURNAL OF HEMATOPATHOLOGY, 2022; 15 (1)
Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous disorder which is less typical in adults than pediatric patients. In ......
期刊： JOURNAL OF HEMATOPATHOLOGY, 2022; 15 (1)
Immature granulocytes (IGs) have significance for the diagnosis of myeloid neoplasms (MNs). The current study aims to use a hematology analyzer to eva......
期刊： JOURNAL OF HEMATOPATHOLOGY, 2022; 15 (3)
Familial hemophagocytic lymphohistiocytosis (FHLH) with Epstein-Barr virus (EBV) infection can mimic chronic active EBV infection of T- and NK-cell ty......
期刊： JOURNAL OF HEMATOPATHOLOGY, 2022; 15 (4)
Congenital hypo-dysfibrinogenemia is a rare autosomal dominant or co-dominant genetic disorder. This study was designed to analyze the clinical phenot......
期刊： JOURNAL OF HEMATOPATHOLOGY, 2022; 15 (1)
The purpose of this study is to explore the clinicopathological features of Kikuchi-Fujimoto disease (KFD) following vaccination against coronavirus d......
期刊： JOURNAL OF HEMATOPATHOLOGY, ; ()
Currently, multiple myeloma is an incurable malignant plasma cell neoplasm, and the incidence rate ranks second in terms of hematological malignancies......
期刊： JOURNAL OF HEMATOPATHOLOGY, 2020; 13 (1)
Decreased ADAMTS-13 is important for the diagnosis of thrombotic thrombocytopenic purpura (TTP), but recent studies have shown that reduced ADAMTS-13 ......
期刊： JOURNAL OF HEMATOPATHOLOGY, 2019; 12 (4)
Extranodal natural killer/T-cell lymphoma (ENKTCL), nasal type, is rare and aggressive and often involves the nose, nasopharynx, and upper aerodigesti......
