- Haploidentical Family Donor Transplantation for Pediatric Hematologic Malignancies
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Lee JW
- KMID: 2522076
- Clin Pediatr Hematol Oncol.
- 2021 Oct;28(2):67-74.
- doi: 10.15264/cpho.2021.28.2.67
Haploidentical family donor hematopoietic stem cell transplantation (Haplo-HSCT) has been increasingly used for patients who require transplant for optimum therapy, but lack a human leukocyte antigen (HLA)-matched donor. Important variables... -
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- Comparison of the Efficacy of Piperacillin/Tazobactam and Meropenem, with or without Intravenous Immunoglobulin, as Second-Line Therapy for Febrile Neutropenia: A Prospective, Randomized Study
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Sano H, Kobayashi R, Matsushima S, Hori D, Yanagi M, Kodama K, Suzuki D, Kobayashi K
- KMID: 2522077
- Clin Pediatr Hematol Oncol.
- 2021 Oct;28(2):75-83.
- doi: 10.15264/cpho.2021.28.2.75
Background: Febrile neutropenia (FN) remains an important complication in pediatric cancer patients. The present study compared the efficacy of meropenem (MEPM) and piperacillin/tazobactam (PIPC/TAZ) with or without intravenous immunoglobulin (IVIG)... -
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- A Pediatric Case of Atypical Chronic Myeloid Leukemia with CSF3R Mutation Not Responding to Ruxolitinib, but Rescued by Allogeneic Transplantation
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Choi YJ, Baek HJ, Kim BR, Park SM, Shin MG, Kook H
- KMID: 2522080
- Clin Pediatr Hematol Oncol.
- 2021 Oct;28(2):93-97.
- doi: 10.15264/cpho.2021.28.2.93
Atypical chronic myeloid leukemia (aCML), BCR-ABL1-negative is a rare myeloid neoplasm, especially in pediatric patients. The mutations identified in aCML have overlapped with those of other myeloid neoplasms. In recent... -
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- RUNX1 Germline Mutation in a Patient with Chronic Thrombocytopenia
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Nam Y, Yeon GM, Kong SG
- KMID: 2522079
- Clin Pediatr Hematol Oncol.
- 2021 Oct;28(2):89-92.
- doi: 10.15264/cpho.2021.28.2.89
One of the pathophysiologic mechanism of inherited thrombocytopenia is a defect in transcription factors that regulate the expression of multiple genes required for megakaryopoiesis. Runt-related transcription factor 1 (RUNX1) binds... -
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- A Case of Adrenal Myelolipoma Associated with Hereditary Spherocytosis
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Gug D, Park HY, Lee BL, Kim KH, Lee JE, Park JK
- KMID: 2522081
- Clin Pediatr Hematol Oncol.
- 2021 Oct;28(2):98-102.
- doi: 10.15264/cpho.2021.28.2.98
Hereditary spherocytosis is the most common hereditary red blood cell membrane disorder. It results from a deficiency in certain proteins that are part of the red blood cell membrane cytoskeleton.... -
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- A Boy with X-Linked Inhibitor of Apoptosis Protein (XIAP) Deficiency as the Initial Presentation of Pure Red Cell Aplasia
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Sim SY, Choi HY, Han SB, Chung NG, Cho B, Kim M, Jeong DC
- KMID: 2522078
- Clin Pediatr Hematol Oncol.
- 2021 Oct;28(2):84-88.
- doi: 10.15264/cpho.2021.28.2.84
X-linked inhibitor of apoptosis protein (XIAP) deficiency is a rare immunodeficiency disorder. A 13-month-old boy was diagnosed with pure red cell aplasia (PRCA) and treated with steroid and cyclosporine. Bone... -
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