- Primary Extragonadal Germ Cell Tumors in Klinefelter Syndrome: 10-Years of Experience from a Single Institute
-
Kim Y, Ahn WK, Han JW, Hahn SM, Kwon SY, Lyu CJ
- KMID: 2500512
- Clin Pediatr Hematol Oncol.
- 2020 Apr;27(1):61-66.
- doi: 10.15264/cpho.2020.27.1.61
Background: Approximately 8% of male patients presenting with primary mediastinal germ cell tumors (GCTs) have Klinefelter syndrome (KS), while patients diagnosed with retroperitoneal GCTs also exhibit a range of chromosomal... -
- CITED
-
- Close
- SHARE
-
- Close
- Immunotherapy in Pediatric Solid Tumors
-
Choi JY
- KMID: 2500508
- Clin Pediatr Hematol Oncol.
- 2020 Apr;27(1):22-31.
- doi: 10.15264/cpho.2020.27.1.22
The survival rates for pediatric patients with solid tumors have improved dramatically in recent decades. However, patients with metastatic disease at diagnosis or progressive solid tumors still have a poor... -
- CITED
-
- Close
- SHARE
-
- Close
- Management of Hepatoblastoma in the Modern Era and Future Perspectives
-
Suh JK, Kang S, Kim H, Koh KN, Im HJ
- KMID: 2500510
- Clin Pediatr Hematol Oncol.
- 2020 Apr;27(1):43-54.
- doi: 10.15264/cpho.2020.27.1.43
Hepatoblastoma is the most common malignant hepatic tumor in infants and young children and accounts for approximately 1% of all pediatric malignancies. A treatment strategy incorporating chemotherapy and surgical resection... -
- CITED
-
- Close
- SHARE
-
- Close
- Immunotherapy in Pediatric Hematologic Malignant Neoplasms
-
Hong KT
- KMID: 2500507
- Clin Pediatr Hematol Oncol.
- 2020 Apr;27(1):14-21.
- doi: 10.15264/cpho.2020.27.1.14
Childhood acute leukemia has achieved tremendous treatment outcome improvement over the past several decades. Given that pediatric leukemia remains the most common type of childhood malignant tumors, there are still... -
- CITED
-
- Close
- SHARE
-
- Close
- Pediatric Palliative Care
-
Kim MS
- KMID: 2500511
- Clin Pediatr Hematol Oncol.
- 2020 Apr;27(1):55-60.
- doi: 10.15264/cpho.2020.27.1.55
In modern medical environment, death rates of newborn babies, children, and adolescents have decreased while the survival rate of life-threatening diseases has increased drastically. The relative 5 year survival rates... -
- CITED
-
- Close
- SHARE
-
- Close
- A Recent Update on Histiocytic Disorder in Children: Focus on Diagnosis and Treatment
-
Yoon HS
- KMID: 2500509
- Clin Pediatr Hematol Oncol.
- 2020 Apr;27(1):32-42.
- doi: 10.15264/cpho.2020.27.1.32
The histiocytosis is rare disorder characterized by the accumulation of macrophages, dendritic cells, or monocyte-derived cells in various tissues and organs of children and adults. Classifying histiocytic disorders is difficult... -
- CITED
-
- Close
- SHARE
-
- Close
- Current Knowledge on Inherited Platelet Function Disorders
-
Jung N, Shim YJ
- KMID: 2500506
- Clin Pediatr Hematol Oncol.
- 2020 Apr;27(1):1-13.
- doi: 10.15264/cpho.2020.27.1.1
Inherited platelet function disorders (IPFDs) are rare and underdiagnosed in individuals with clinically significant bleeding diathesis. IPFDs are classified according to the causative molecular defects involved in the process of... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Von Hippel-Lindau Disease Presented with Multiple Pancreatic Cysts and Medullary Hemangioblastoma
-
Kim YH, Jung HL, Yang A, Kwak JH, Kim DS, Shim JY, Shim JW
- KMID: 2500513
- Clin Pediatr Hematol Oncol.
- 2020 Apr;27(1):67-71.
- doi: 10.15264/cpho.2020.27.1.67
Von Hippel-Lindau (VHL) disease is a rare inherited cancer predisposition syndrome characterized by benign and malignant tumors in multiple organs, especially cerebellar hemangioblastomas, retinal angiomas, renal-cell carcinoma, and pheochromocytomas. Clinically,... -
- CITED
-
- Close
- SHARE
-
- Close
