- Large Hepatocellular Adenoma Presenting with Iron Deficiency Anemia: A Case Report
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Koh YK, Yoon SH, Kang SH, Kim H, Im HJ, Ha S, Namgoong JM, Koh KN
- KMID: 2542112
- Clin Pediatr Hematol Oncol.
- 2023 Apr;30(1):25-29.
- doi: 10.15264/cpho.2023.30.1.25
Hepatocellular adenoma is an uncommon, benign liver tumor usually occurring in patients using estrogen or anabolic androgens and in those with a genetic disease, including glycogen storage disease. Hepatocellular adenomas... -
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- Acute Complications of Pediatric Allogeneic Hematopoietic Stem Cell Transplantation and Their Effects on Survival: A Single-Center Experience in Korea
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Lee KM, Ahn WK, Han JW, Lyu CJ, Hahn SM
- KMID: 2542110
- Clin Pediatr Hematol Oncol.
- 2023 Apr;30(1):11-20.
- doi: 10.15264/cpho.2023.30.1.11
Background: Acute complications within 100 days after allogeneic hematopoietic stem cell transplantation (HSCT) can increase immediate mortality as well as the risk of chronic complications and morbidity. A comprehensive review... -
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- Intralobar Nephroblastomatosis Mimicking Wilms Tumor Treated with Chemotherapy after Removal of the Affected Kidney
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Sano H, Kobayashi R, Matsushima S, Hori D, Yanagi M, Suzuki D, Ohba G, Yamamoto H, Kobayashi K
- KMID: 2542111
- Clin Pediatr Hematol Oncol.
- 2023 Apr;30(1):21-24.
- doi: 10.15264/cpho.2023.30.1.21
Nephroblastomatosis (NBM) is a precursor of Wilms tumor. We herein report a case in which Wilms tumor was initially suspected and the affected kidney was removed. The tumor was subsequently diagnosed... -
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- SARS-CoV-2 Infection Mimicking Neutropenic Fever during Chemotherapy for Acute Lymphoblastic Leukemia: A Case Report
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Kang HS
- KMID: 2542116
- Clin Pediatr Hematol Oncol.
- 2023 Apr;30(1):47-51.
- doi: 10.15264/cpho.2023.30.1.47
Children with SARS-CoV-2 infection typically exhibit mild respiratory symptoms, with only a small proportion presenting with gastrointestinal symptoms. However, children and adolescents with cancer may develop severe illnesses when infected... -
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- Beta-Thalassemia with Initial Presentation as Immune Thrombocytopenia: A Case Report
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Kang HS
- KMID: 2542115
- Clin Pediatr Hematol Oncol.
- 2023 Apr;30(1):42-46.
- doi: 10.15264/cpho.2023.30.1.42
Immune thrombocytopenia (ITP) is characterized by a low platelet count caused by immune-mediated platelet destruction. In children, ITP usually resolves on its own within three months, but treatment may be... -
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- Recent Advances in Diagnostic and Surveillance Strategies for Childhood Cancer Predisposition Syndromes
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Yoo JW
- KMID: 2542109
- Clin Pediatr Hematol Oncol.
- 2023 Apr;30(1):1-10.
- doi: 10.15264/cpho.2023.30.1.1
Cancer predisposition syndromes (CPS) are a group of genetic disorders that increase the risk of developing various types of cancer. The prevalence of CPS in children has been known to... -
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- Thrombotic Thrombocytopenic Purpura as the First Symptom of Systemic Lupus Erythematosus: A Case Report with Review of Literature
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Jo YM, So CH, Choi DY
- KMID: 2542113
- Clin Pediatr Hematol Oncol.
- 2023 Apr;30(1):30-35.
- doi: 10.15264/cpho.2023.30.1.30
Thrombotic thrombocytopenic purpura (TTP) can cause serious morbidity and mortality, and differentiating between this disease and systemic lupus erythematosus (SLE) can prove challenging. Although rare, TTP accompanied by SLE is... -
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- Long-Term Anticoagulation Therapy for Antiphospholipid Syndrome Following Unsuccessful Arterial Thrombosis Stent Procedure: A Case Report
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Kang HS
- KMID: 2542114
- Clin Pediatr Hematol Oncol.
- 2023 Apr;30(1):36-41.
- doi: 10.15264/cpho.2023.30.1.36
Antiphospholipid syndrome (APS) is an autoimmune, multisystemic disorder marked by arterial, venous, or small-vessel thromboembolic events and persistence of antiphospholipid antibodies (aPL). Approximately 50% of APS patients exhibit primary disease... -
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