Peripheral primitive neuroectodermal tumour meaning

Peripheral primitive neuroectodermal tumour is a type of cancer that arises in the soft tissues and bones of the body.


Peripheral primitive neuroectodermal tumour definitions

Word backwards larehpirep evitimirp lamredotceoruen ruomut
Part of speech Noun
Syllabic division pe-ri-pher-al pri-mi-tive neu-ro-ec-tod-er-mal tu-mour
Plural The plural of the word peripheral primitive neuroectodermal tumour is peripheral primitive neuroectodermal tumours.
Total letters 40
Vogais (5) e,i,a,u,o
Consonants (10) p,r,h,l,m,t,v,n,c,d

Peripheral Primitive Neuroectodermal Tumour

Peripheral Primitive Neuroectodermal Tumour (PNET) is a rare type of cancer that affects the soft tissues, bones, and connective tissues, primarily in children and young adults. PNETs belong to the Ewing sarcoma family of tumors and are characterized by aggressive growth.

Symptoms and Diagnosis

Symptoms of PNET may include pain, swelling, and a lump in the affected area. Other symptoms depend on the location of the tumor. Diagnosis often involves imaging tests such as X-rays, CT scans, or MRIs, along with a biopsy to confirm the presence of PNET.

Treatment Options

Treatment for PNET typically involves a combination of surgery, chemotherapy, and radiation therapy. The specific treatment plan will depend on the location and stage of the tumor, as well as the overall health of the patient. In some cases, targeted therapy or immunotherapy may also be used.

Prognosis and Survival Rate

The prognosis for PNET can vary depending on factors such as the size of the tumor, its location, and whether it has spread to other parts of the body. Overall, the survival rate for PNET is relatively low, especially in cases where the cancer is diagnosed at a later stage.

Research and Advances

Ongoing research into PNET is focused on developing more targeted and effective treatments, as well as improving early detection methods. Clinical trials are also being conducted to test new therapies and treatment approaches for PNET patients.

In conclusion, Peripheral Primitive Neuroectodermal Tumour is a rare and aggressive type of cancer that requires a multidisciplinary approach to treatment. Early detection and a personalized treatment plan are crucial in improving outcomes for patients with PNET.


Peripheral primitive neuroectodermal tumour Examples

  1. Doctors diagnosed the patient with a peripheral primitive neuroectodermal tumour after conducting a biopsy.
  2. Treatment for peripheral primitive neuroectodermal tumour often involves surgery, chemotherapy, and radiation therapy.
  3. Researchers are studying new targeted therapies for peripheral primitive neuroectodermal tumour.
  4. Patients with peripheral primitive neuroectodermal tumour may experience symptoms such as pain, swelling, and fatigue.
  5. Survival rates for peripheral primitive neuroectodermal tumour vary depending on the stage of the cancer at diagnosis.
  6. Support groups can provide emotional support for individuals living with peripheral primitive neuroectodermal tumour.
  7. Early detection of peripheral primitive neuroectodermal tumour is crucial for successful treatment outcomes.
  8. Patients undergoing treatment for peripheral primitive neuroectodermal tumour may require frequent monitoring by their healthcare team.
  9. Family history may play a role in the development of peripheral primitive neuroectodermal tumour.
  10. Clinical trials are investigating new therapies for peripheral primitive neuroectodermal tumour.


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  • Updated 24/04/2024 - 20:19:44