Onkologi Hematologi


1494809702600_crop_944x498100 KASUS ONKOLOGI HEMATOLOGI ANAK


Acute Porphyria
Alpha Thalassemia
Antithrombin III Deficiency
Bernard-Soulier Syndrome
Consumption Coagulopathy
Cutaneous Porphyria
Donath-Landsteiner Hemolytic Anemia
Evans Syndrome
Fanconi Anemia
Hemophilia C
Hereditary Disorders of Red Cell Permeability
Inherited Abnormalities of Fibrinogen
Kasabach-Merritt Syndrome
May-Hegglin Anomaly
Pearson Syndrome
Acute Anemia
Autoimmune and Chronic Benign Neutropenia
Chronic Anemia
Chronic Granulomatous Disease
Factor VII Deficiency
Factor XIII Deficiency
Hereditary Elliptocytosis and Related Disorders
Megaloblastic Anemia
Polycythemia Vera
Von Willebrand Disease
Pelger-Huet Anomaly
Shwachman-Diamond Syndrome
Thalassemia Intermedia
Thrombocytopenia-Absent Radius Syndrome
Transient Erythroblastopenia of Childhood
Tropical Splenomegaly Syndrome
White Blood Cell Function


Carcinoid Tumor
Chemotherapy-Induced Nausea and Vomiting
Childhood Cancer Epidemiology
Childhood Cancer Genetics
Clear Cell Sarcoma of the Kidney
Ewing Sarcoma
Late Effects of Childhood Cancer and Treatment
Li-Fraumeni Syndrome
Long-Term Effects of Bone Marrow Transplantation
Lymphohistiocytosis (Hemophagocytic Lymphohistiocytosis)
Lymphoproliferative Disorders
Malignant Rhabdoid Tumor
Marrow Failure Syndromes
Nasopharyngeal Cancer
Nonrhabdomyosarcoma Soft Tissue Sarcomas
Acute Lymphoblastic Leukemia
Acute Myelocytic Leukemia
Colorectal Tumors
Hepatocellular Carcinoma
Hodgkin Lymphoma
Liver Tumors
Myelodysplastic Syndrome
Non-Hodgkin Lymphoma
Veno-occlusive Hepatic Disease
WAGR Syndrome
Wilms Tumor

Bone and soft tissue tumors

  • Bone sarcomas: Preoperative evaluation, histologic classification, and principles of surgical management
  • Bone tumors: Diagnosis and biopsy techniques
  • Chemotherapy and radiation therapy in the management of osteosarcoma
  • Clinical presentation, staging, and prognostic factors of the Ewing sarcoma family of tumors
  • Epidemiology, pathology, and molecular genetics of the Ewing sarcoma family of tumors
  • Intradural nerve sheath tumors
  • Langerhans cell histiocytosis (eosinophilic granuloma) of bone in children and adolescents
  • Osteosarcoma: Epidemiology, pathogenesis, clinical presentation, diagnosis, and histology
  • Radiation therapy for Ewing sarcoma family of tumors
  • Rhabdomyosarcoma in childhood and adolescence: Epidemiology, pathology, and molecular pathogenesis
  • Treatment of the Ewing sarcoma family of tumors

Cancer survivors

  • Endocrinopathies in the childhood cancer survivor

Central nervous system tumors

  • Acute complications of cranial irradiation
  • Classification and pathologic diagnosis of gliomas
  • Clinical features, diagnosis, and management of von Hippel-Lindau disease
  • Clinical manifestations and diagnosis of central nervous system tumors in children
  • Clinical presentation, diagnosis, and risk stratification of medulloblastoma
  • Clinical presentation, diagnosis, and staging evaluation of neuroblastoma
  • Craniopharyngioma
  • Diffuse intrinsic pontine glioma
  • Ependymoma
  • Epidemiology of central nervous system tumors in children
  • Epidemiology, pathogenesis, and pathology of neuroblastoma
  • Focal brainstem glioma
  • Hemangioblastoma
  • Histopathology and molecular pathogenesis of medulloblastoma
  • Intracranial germ cell tumors
  • Management of low-grade glioma
  • Molecular biology and pathogenesis of von Hippel-Lindau disease
  • Optic pathway glioma
  • Overview of the management of central nervous system tumors in children
  • Pineal gland masses
  • Risk factors for brain tumors
  • Sacrococcygeal germ cell tumors
  • Treatment and prognosis of medulloblastoma
  • Treatment and prognosis of neuroblastoma
  • Uncommon brain tumors

Complications of cancer and its therapy

  • Bone problems in childhood cancer patients
  • Cardiotoxicity of nonanthracycline cancer chemotherapy agents
  • Fever in children with chemotherapy-induced neutropenia
  • Immunizations in patients with cancer
  • Pediatric palliative care
  • Prevention and treatment of chemotherapy-induced nausea and vomiting in adults
  • Therapeutic use and toxicity of high-dose methotrexate
  • Thromboembolism in children with cancer
  • Tumor lysis syndrome: Definition, pathogenesis, clinical manifestations, etiology and risk factors
  • Tumor lysis syndrome: Prevention and treatment

Endocrine tumors

  • Pheochromocytoma in children
  • Treatment of adrenocortical carcinoma


  • Clinical assessment of the child with suspected cancer
  • Evaluation and management of pain in children

Genetic diseases

  • Tuberous sclerosis complex: Genetics, clinical features, and diagnosis
  • Tuberous sclerosis complex: Management

Genitourinary tumors

  • Ovarian germ cell tumors: Pathology, clinical manifestations, and diagnosis
  • Presentation, diagnosis, and staging of Wilms tumor
  • Treatment and prognosis of Wilms tumor
  • Treatment of malignant germ cell tumors of the ovary

Hematologic malignancies

  • Clinical manifestations, pathologic features, and diagnosis of Langerhans cell histiocytosis
  • Epidemiology, clinical manifestations, pathologic features, and diagnosis of Burkitt lymphoma
  • Juvenile myelomonocytic leukemia
  • Overview of Hodgkin lymphoma in children and adolescents
  • Overview of the outcome of acute lymphoblastic leukemia in children and adolescents
  • Overview of the presentation and diagnosis of acute lymphoblastic leukemia in children and adolescents
  • Overview of the treatment of acute lymphoblastic leukemia in children and adolescents
  • Primary lymphoma of bone
  • Risk group stratification and prognosis for acute lymphoblastic leukemia in children and adolescents
  • Treatment of Burkitt leukemia/lymphoma in adults
  • Treatment of nodular lymphocyte-predominant Hodgkin lymphoma


  • Clinical presentation, diagnosis, and staging evaluation of neuroblastoma
  • Epidemiology, pathogenesis, and pathology of neuroblastoma
  • Treatment and prognosis of neuroblastoma

Tumors of the eye and orbit

  • Retinoblastoma: Clinical presentation, evaluation, and diagnosis
  • Retinoblastoma: Treatment and outcome



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