- Subcutaneous Panniculitis-Like T-Cell Lymphoma with Hemophagocytic Syndrome in a Child: A Successful Treatment with the BFM-NHL-90 Protocol
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Kim S, Kim A, Hah JO
- KMID: 2508201
- Clin Pediatr Hematol Oncol.
- 2020 Oct;27(2):129-133.
- doi: 10.15264/cpho.2020.27.2.129
Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a distinct cutaneous lymphoma subtype that is characterized by pleomorphic T-cell infiltration of the subcutaneous tissue. SPTCL is usually associated with indolent clinical course.... -
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- A Case of Wilms Tumor with a Tumor Thrombus in a Boy with WAGR Syndrome
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Lee S, Kim HJ, Jeon Is
- KMID: 2508202
- Clin Pediatr Hematol Oncol.
- 2020 Oct;27(2):134-137.
- doi: 10.15264/cpho.2020.27.2.134
Intravascular extension of Wilms tumor (WT) can occur in approximately 4-10% of patients. In general, it does not cause any clinical problems because most of these tumors are small. Although... -
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- Burkitt Lymphoma Initially Presenting as Acute Pancreatitis in an Adolescent Boy
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Kim H, Kwon Y, Kim ES, Ju HY, Koo HH, Choe YH, Kim MJ
- KMID: 2508200
- Clin Pediatr Hematol Oncol.
- 2020 Oct;27(2):124-128.
- doi: 10.15264/cpho.2020.27.2.124
In children and adolescents, acute pancreatitis is a rare cause of abdominal pain. The causes of pancreatitis in children are various including infection and drugs, but the overall cause of this... -
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- Pathology of Peripheral Neuroblastic Tumors
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Shimada H, Sano H, Hazard FK
- KMID: 2508195
- Clin Pediatr Hematol Oncol.
- 2020 Oct;27(2):73-86.
- doi: 10.15264/cpho.2020.27.2.73
Peripheral neuroblastic tumors (pNTs including Neuroblastoma, Ganglioneuroblastoma and Ganglioneuroma) are biologically and clinically heterogeneous. In order to develop efficient clinical treatment protocols of this disease, patients are stratified into different... -
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- Minimal Residual Disease Detection in Pediatric Acute Lymphoblastic Leukemia
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Kim M, Park CJ
- KMID: 2508196
- Clin Pediatr Hematol Oncol.
- 2020 Oct;27(2):87-100.
- doi: 10.15264/cpho.2020.27.2.87
Minimal residual disease (MRD) status is the strongest independent prognostic factor for patients with pediatric acute lymphoblastic leukemia (ALL). Monitoring of the MRD status allows risk-adapted therapy as its absence... -
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- Iron Deficiency Anemia
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Lee NH
- KMID: 2508197
- Clin Pediatr Hematol Oncol.
- 2020 Oct;27(2):101-112.
- doi: 10.15264/cpho.2020.27.2.101
Iron deficiency anemia (IDA) is a common medical problem that affects an estimated 30-50% of the world’s population. The causes of IDA are malnutrition, rapid growth with improper dietary iron,... -
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- A Case of Hereditary Spherocytosis Initially Manifested as an Aplastic Crisis Caused by Parvovirus B19 Infection
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Jin H, Lee JW, Ju HY, Cho HW, Hyun JK, Sung KW, Koo HH, Kim HJ, Yoo KH
- KMID: 2508199
- Clin Pediatr Hematol Oncol.
- 2020 Oct;27(2):120-123.
- doi: 10.15264/cpho.2020.27.2.120
Hereditary spherocytosis (HS) is the most common inherited red cell membrane disorder. Its main laboratory finding is anemia with reticulocytosis. However, in the case of an aplastic crisis, there may... -
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- Perioperative Management and Outcomes in Children with Hereditary Bleeding Disorder: a Retrospective Review at a Single Hemophilia Treatment Center
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Chon HN, Cho JH, Park YS
- KMID: 2508198
- Clin Pediatr Hematol Oncol.
- 2020 Oct;27(2):113-119.
- doi: 10.15264/cpho.2020.27.2.113
Background: Establishing hemostasis for surgical procedures in children with hereditary bleeding disorders is challenging. We evaluated the results of surgical procedures in children with hereditary bleeding disorders at our center... -
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