Challenges and practical considerations in the management of blastic plasmacytoid dendritic cell neoplasm: A single-center experience [0.03%]
关于颗粒细胞浆样树突状细胞肿瘤管理的挑战及实际问题：单中心经验报告
Haripriya Andanamala,Naveen Pemmaraju,Taha Al-Juhaishi
Haripriya Andanamala
Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) is a rare and often life-threatening complex hematologic malignancy that can commonly infiltrate the skin, lymph nodes, central nervous system, and bone marrow. In the setting of the infr...
A novel mutation of LYST and haemophagocytic lymphohistiocytosis as the first symptom in children with ph+ALL: A case report and literature review [0.03%]
LYST新型突变导致的噬血细胞综合征作为儿童Ph⁺急性淋巴细胞白血病（ALL）的首发症状：一例报告及文献复习
Tiantian Wang,Xuhui Liu,Li Lin et al.
Tiantian Wang et al.
Haemophagocytic lymphohistiocytosis (HLH) is a rare disorder. This study sheds light on a rare and intriguing case of HLH as the initial symptom in a child with Philadelphia chromosome-positive acute lymphoblastic leukaemia (ph+ALL). This c...
Septic arthritis as breakthrough invasive fusariosis after cord blood transplantation [0.03%]
脐带血移植后突破性侵袭性念珠菌病导致的化脓性关节炎
Shinichi Katsuoka,Hidehiro Itonaga,Yasushi Sawayama et al.
Shinichi Katsuoka et al.
A 63-year-old male received a third allogeneic hematopoietic stem cell transplantation with voriconazole prophylaxis for relapsed acute myeloid leukemia. He developed septic arthritis without any typical skin lesions due to fungal infection...
Venetoclax for an ATRA and ATO resistance acute promyelocytic leukemia patient with TNRC18::RARA fusion gene [0.03%]
用于携带TNRC18::RARA融合基因的ATRA和ATO耐药急性早幼粒细胞白血病患者的维奈克拉治疗
Weina Li,Haijie Li,Xueyan Chen et al.
Weina Li et al.
Variant acute promyelocytic leukemia (APL) poses diagnostic and therapeutic challenges primarily because of the absence of PML::RARA. This report presents the case of a patient diagnosed with all-trans retinoic acid (ATRA)-resistant APL har...
Diagnostic challenges in classification of plasmacytoid dendritic cell proliferation associated with acute myeloid leukemia in the context of secondary-type mutations [0.03%]
具有二次型突变背景下与急性髓系白血病相关的浆细胞样树突状细胞增殖的分类诊断挑战
Iran Rashedi,Yasmeen Abulkhair,Eric Diehl et al.
Iran Rashedi et al.
Successful treatment of a CLL associated IgM hyper-viscosity syndrome: A rare case [0.03%]
一例罕见的CLL相关IgM高黏滞血症成功治疗病例报告
Toufic Tannous,Gil Hevroni,Raiyan Islam et al.
Toufic Tannous et al.
In the context of chronic lymphocytic leukemia (CLL), Hyperviscosity Syndrome (HVS) typically arises from hyperleukocytosis, although it infrequently stems from IgM hyperparaproteinemia. We present a distinctive case of HVS induced by IgM h...
Acute myeloid leukemia with a ZMYND11:: MBTD1 fusion gene following chemotherapy and radiotherapy for breast cancer: A case report [0.03%]
化疗和放疗治疗乳腺癌后出现ZMYND11::MBTD1融合基因的急性髓系白血病一例报告
Hidetsugu Kawai,Sawako Shiraiwa,Daisuke Ogiya et al.
Hidetsugu Kawai et al.
The t(10;17)(p15;q21) translocation is a very rare recurrent cytogenetic aberration, and produced ZMYND11::MBTD1 fusion gene. To date, nine cases of acute leukemia with the t(10;17)(p15;q21) translocation have been reported, but the case of...
Successful treatment of AML using non-intensive chemotherapy in Jehovah's Witness patients [0.03%]
对不愿输血的AML患者的非强化化疗治疗效果良好：见证者患者中的经验
David Page,Daniel Sawler,Joseph Brandwein
David Page
Acute myeloid leukemia (AML) patients undergoing induction chemotherapy receive transfusion support to manage severe cytopenias and associated sequelae. Jehovah's Witness (JW) patients typically decline transfusion of most or all blood prod...
Two cases of AMeD syndrome with isochromosome 1q treated with allogeneic stem cell transplantation [0.03%]
两例1号染色体长臂等臂染色体所致AMeD综合征的异基因造血干细胞移植治疗报告
Mari Kagajo,Kyoko Moritani,Mayumi Iwamoto et al.
Mari Kagajo et al.
AMeD syndrome is characterized by aplastic anemia, mental retardation, short stature, and microcephaly and is caused by digenic mutations in the aldehyde dehydrogenase 2 (ALDH2) and alcohol dehydrogenase 5 (ADH5) genes. We have successfully...
Very late relapse of Burkitt's lymphoma in an EBV-negative patient after 20 years of complete remission [0.03%]
一名EB病毒阴性的患者在20年完全缓解后出现伯基特淋巴瘤晚期复发
Kmar Mrad,Nader Slama,Nouha Ben Abdeljalil et al.
Kmar Mrad et al.
Burkitt's lymphoma (BL) is an aggressive B-cell lymphoma that occurs in children and adults. It is a chemosensitive lymphoma with very exceptional cases of late relapse. We report the case of a 32-year-old male, originally from a nonendemic...