Fat Embolism Syndrome Mimicking Thrombotic Thrombocytopenic Purpura in a Patient With Hemoglobin S/Beta-Thalassemia [0.03%]
一名HbS/β-地中海贫血患者发生模仿血栓性血小板减少性紫癜的脂肪栓塞综合征
Bobby Se,Austin Frisch,Min Woo Hwang et al.
Bobby Se et al.
Thrombotic microangiopathies cause ischemic organ damage and require urgent management for a favorable prognosis. Fat embolism syndrome from bone marrow necrosis is a rare and unique pathology that carries a high mortality rate. It can mimi...
Case Reports
Journal of hematology. 2024 Jun;13(3):104-107. DOI:10.14740/jh1274 2024
Characterization and Clinical Assessment of a Peculiar Case of Hemolytic Anemia [0.03%]
一例溶血性贫血的诊治体会
Fulvio Castelgrande,Gemma Viola,Cinzia Calabrese et al.
Fulvio Castelgrande et al.
Thalassemic diseases are characterized by a reduced (β+) or absent (β0) synthesis of the globin chains of hemoglobin (Hb) due to genetic mutations. β-thalassemia was more frequent in the Mediterranean area, but now it is diffused worldwi...
Case Reports
Journal of hematology. 2024 Jun;13(3):108-115. DOI:10.14740/jh1204 2024
Predictors of Non-Variceal Hemorrhage in a National Cohort of Patients With Chronic Liver Disease [0.03%]
慢性肝病患者全国队列非曲张静脉出血的预测因素
Amber Afzal,Preethi Kesavan,Luo Suhong et al.
Amber Afzal et al.
Background: Non-variceal hemorrhage in patients with chronic liver disease (CLD) increases morbidity, mortality, and healthcare costs. There are limited data on risk factors for non-variceal hemorrhage in the CLD populati...
Hepatosplenic Alpha-Beta T-Cell Lymphoma: A Challenging Diagnostic Entity [0.03%]
肝脾T细胞淋巴瘤：一个具有挑战性的诊断实体
Abanoub Gabra,Joanna Polanco,Shrija Thapa et al.
Abanoub Gabra et al.
Hepatosplenic T-cell lymphoma (HSTCL) is rare and clinically very aggressive T-cell lymphoma. The majority of cases harbor γδ T-cell receptors (TCRs); however, in some even rarer cases, tumor cells harbor αβ TCR. Recent studies suggest ...
Case Reports
Journal of hematology. 2024 Apr;13(1-2):29-33. DOI:10.14740/jh1203 2024
Natural Anticoagulant Protein Levels in Patients With Beta-Thalassemia Major: A Case-Control Study [0.03%]
重型β地中海贫血患者中天然抗凝蛋白水平的病例对照研究
Abbas Ahmadi,Soudabeh Hosseini,Akbar Dorgalaleh et al.
Abbas Ahmadi et al.
Background: β-thalassemia is a group of inherited blood disorders that affect the production of β-globin chains, leading to the reduction or absence of these chains. One of the complications observed in patients with β...
Successful Treatment of Refractory Post-Transplant Lymphoproliferative Disorder With Chimeric Antigen Receptor T-Cell Therapy in a Heart Transplant Recipient [0.03%]
嵌合抗原受体T细胞治疗成功治愈1例难治性心脏移植后淋巴增殖性疾病患者
Katherine Hickmann,Ryan Sweeney,Chelsea Peterson et al.
Katherine Hickmann et al.
Post-transplant lymphoproliferative disorders (PTLDs) are opportunistic malignancies that complicate the success of hematopoietic stem cell or solid organ transplantation. These disorders often arise post-transplant due to the immunosuppres...
Case Reports
Journal of hematology. 2024 Apr;13(1-2):34-38. DOI:10.14740/jh1211 2024
Clinical Efficacy of Programmed Cell Death Ligand 1 Antibody in Treatment of Extranodal Natural Killer/T-Cell Lymphoma With Hemophagocytic Lymphohistiocytosis [0.03%]
程序性死亡配体1抗体治疗噬血细胞综合征型外周T/NK细胞淋巴瘤的疗效分析
Chun Li Yang,Xi Chen,Hui Jie Zhou et al.
Chun Li Yang et al.
Extranodal natural killer/T-cell lymphoma-associated hemophagocytic lymphohistiocytosis (ENKTCL-LAHS) is a rare disease with poor prognosis. Currently, there are no well-established treatments for LAHS. Almost 50% of patients experience rel...
Case Reports
Journal of hematology. 2024 Apr;13(1-2):46-51. DOI:10.14740/jh1242 2024
Effective Management of Polycythemia Vera With Ropeginterferon Alfa-2b Treatment [0.03%]
罗匹戈干扰素α-2b治疗真性红细胞增多症的有效管理
Shan Shan Suo,Rong Feng Fu,Albert Qin et al.
Shan Shan Suo et al.
Background: Polycythemia vera (PV) is a myeloproliferative neoplasm. Ropeginterferon alfa-2b is a new-generation polyethylene glycol-conjugated proline-interferon. It is approved for the treatment of PV at a starting dose...
Middle Meningeal Artery Embolization in Acute Leukemia Patients Presenting With Subdural Hematoma [0.03%]
急性白血病患者出现硬膜下血肿的脑膜中动脉栓塞治疗
Binoy Yohannan,Juan Carlos Martinez Gutierrez,Peng Roc Chen et al.
Binoy Yohannan et al.
Intracerebral hemorrhage is a potentially fatal complication in patients with acute leukemia and contributing factors include thrombocytopenia and coagulopathy. Patients with acute leukemia may develop subdural hematoma (SDH) spontaneously ...
Case Reports
Journal of hematology. 2024 Apr;13(1-2):39-45. DOI:10.14740/jh1215 2024
Anorectal Infections in Neutropenic Leukemia Patients: A Common Clinical Challenge [0.03%]
中性粒细胞减少的白血病患者的肛门直肠感染：一个常见的临床挑战
Rodrick Babakhanlou,Farhad Ravandi-Kashani,Angel G Hita et al.
Rodrick Babakhanlou et al.
Anorectal infections in neutropenic leukemia patients are a significant and potentially life-threatening complication. The pathogenesis of this condition is not entirely understood and believed to be multifactorial, including mucosal injury...