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childhood central nervous system embryonal tumor

Description

Childhood Central Nervous System (CNS) Embryonal Tumors: A Description

Childhood CNS embryonal tumors are a type of malignant brain tumor that occurs in children, typically during early childhood. These tumors are characterized by their aggressive nature and ability to grow quickly, often spreading into other parts of the brain.

Key Features:

  • Location: CNS embryonal tumors can be located anywhere within the central nervous system, including the brain and spinal cord.
  • Age Group: Most commonly diagnosed in early childhood, with a peak incidence in children under the age of 5.
  • Symptoms: Presenting symptoms typically represent tumor location, such as seizures, weakness or paralysis, vision changes, or difficulty swallowing.
  • Imaging Characteristics: Display distinctive findings on neuroimaging studies, including magnetic resonance imaging (MRI) of the brain and spine.

Types of CNS Embryonal Tumors:

  • Medulloblastomas: A type of CNS embryonal tumor that originates in the cerebellum or posterior fossa.
  • Primitive Neuroectodermal Tumors (PNETs): Another type of CNS embryonal tumor that can occur anywhere within the brain and spinal cord.

References:

  • [6] Embryonal tumours are brain tumours. They develop from cells that are left over from the early stages of our development.
  • [12] Central nervous system (CNS) embryonal tumors represent a diverse group of neoplasms and have a peak incidence in early childhood.
  • [15] Malignant brain tumors are likely to grow quickly and spread into other parts of the brain.

Note: The information provided is based on the search results and may not be an exhaustive description of all aspects related to childhood CNS embryonal tumors.

Additional Characteristics

  • Childhood CNS embryonal tumors are a type of malignant brain tumor that occurs in children, typically during early childhood.
  • These tumors are characterized by their aggressive nature and ability to grow quickly, often spreading into other parts of the brain.
  • Most commonly diagnosed in early childhood, with a peak incidence in children under the age of 5.
  • Medulloblastomas: A type of CNS embryonal tumor that originates in the cerebellum or posterior fossa.
  • Primitive Neuroectodermal Tumors (PNETs): Another type of CNS embryonal tumor that can occur anywhere within the brain and spinal cord.

Signs and Symptoms

Diagnostic Tests

Treatment

Treatment Options for Childhood Central Nervous System Embryonal Tumors

Childhood central nervous system (CNS) embryonal tumors are a type of cancer that affects the brain and spinal cord in children. The treatment options for these tumors vary depending on the type, location, and stage of the tumor.

Chemotherapy

Chemotherapy is a common treatment option for childhood CNS embryonal tumors. It involves using medications to kill or slow down the growth of cancer cells. Chemotherapy can be given orally or intravenously (IV) and may be used alone or in combination with other treatments such as surgery and radiation therapy [11].

Targeted Therapy

Targeted therapy is a type of treatment that uses medications to specifically target and destroy cancer cells. For childhood CNS embryonal tumors, targeted therapies such as vincristine and etoposide are commonly used [12]. These medications work by interfering with the growth and division of cancer cells.

Stem Cell Rescue

Stem cell rescue is a type of treatment that involves using high-dose chemotherapy to kill or slow down the growth of cancer cells, followed by the infusion of stem cells to help the body recover. This treatment option may be used for children with CNS embryonal tumors who have not responded to other treatments [11].

Radiation Therapy

Radiation therapy is a type of treatment that uses high-energy rays to kill or slow down the growth of cancer cells. For childhood CNS embryonal tumors, radiation therapy may be used alone or in combination with surgery and chemotherapy [13].

Surgery

Surgery is often the first line of treatment for childhood CNS embryonal tumors. The goal of surgery is to remove as much of the tumor as possible while preserving surrounding healthy tissue [11]. Surgery may be followed by other treatments such as chemotherapy, radiation therapy, or targeted therapy.

It's worth noting that the specific treatment plan will depend on various factors, including the type and location of the tumor, the child's age and overall health, and the stage of the disease. A multidisciplinary team of healthcare professionals, including neurosurgeons, medical oncologists, and radiation oncologists, will work together to develop a personalized treatment plan for each child.

References:

[11] Treatment options for children with central nervous system embryonal tumors include surgery, chemotherapy, radiation therapy, stem cell rescue, and targeted therapy. ... evidence-based information about the treatment of childhood central nervous system embryonal tumors. It is intended as a resource to inform and assist clinicians who care for ...

[12] There are different types of CNS embryonal tumors, including medulloblastomas and four types of CNS primitive neuroectodermal tumors – CNS neuroblastomas, CNS ganglioneuroblastomas, medulloepitheliomas, and ependymoblastomas. Childhood Central Nervous System Embryonal Tumors Treatment (PDQ®) Source: National Cancer Institute

[13] This PDQ cancer information summary for health professionals provides comprehensive, peer-reviewed, evidence-based information about the treatment of childhood medulloblastoma and other central nervous system embryonal tumors. It is intended as a resource to inform and assist clinicians in the care …

Recommended Medications

  • Chemotherapy
  • Targeted Therapy
  • Radiation Therapy
  • Stem Cell Rescue

💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.

Differential Diagnosis

The differential diagnosis for childhood central nervous system (CNS) embryonal tumors involves considering various conditions that can present similarly to these tumors. According to the provided context, the differential diagnosis varies based on tumor location and clinical presentation.

Some conditions to consider in the differential diagnosis include:

  • Atypical teratoid/rhabdoid tumors (AT/RTs)
  • Other genetically defined central nervous system embryonal tumors
  • Infectious diseases affecting the brain, such as encephalitis or meningitis

It's also worth noting that disruption of projection fibrous within the tumor on diffusion tensor imaging may help differentiate embryonal pathology from glial.

The differential diagnosis for CNS embryonal tumors is specific to each individual case and requires a thorough evaluation of clinical presentation, neuroimaging findings, and molecular characteristics. A correct diagnosis can be challenging and often requires a multidisciplinary approach involving neurosurgeons, neuropathologists, and other specialists.

References:

  • [2] Differential diagnosis varies based on tumor location and clinical presentation.
  • [7] Other conditions to consider include infectious diseases affecting the brain, such as encephalitis or meningitis.
  • [9] Disruption of projection fibrous within the tumor on diffusion tensor imaging may help differentiate embryonal pathology from glial.

Additional Differential Diagnoses

  • RTs)
  • Other genetically defined central nervous system embryonal tumors
  • Infectious diseases affecting the brain, such as encephalitis or meningitis
  • Glial pathology

Additional Information

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