what's the difference in stage 4 gastrointestinal cancer survival rate

What's the difference in stage 4 gastrointestinal cancer survival rate

Too to leukemia, brain tumor, and bone cancer, young children are at risk of developing GI cancer. Learn more about digestive tract cancer in children and spread awareness. Remember that early detection and early treatment can save our children.

Childhood is the most beautiful of all seasons! But not every child is lucky enough to enjoy a carefree childhood. For children battling cancer, hosting at a young age can be difficult. It is important to remember that early diagnosis and early medical treatment can help save a child and cure them of cancer.

To spread awareness about childhood cancer, promote the benefits of early diagnosis and raise funds for families dealing with childhood cancer, India observes Childhood Cancer Awareness Month.

Childhood Cancer: Understanding a Threatening Problem 300,000 children get cancer every year. This is 3-4% of the total annual cancer cases detected worldwide. If Indian statistics, doctors diagnose 40,000-50,000 cases of cancer in children every year. Although 70-90% of childhood cancers are curable, estimates suggest that 70% of children in India die due to:

1. Lack of awareness

2. Late detection and diagnosis

3. Inaccessibility of medical facilities

4. High cost of treatment

5. Unavailability of supportive care.

  What types of digestive tract cancer do children develop?

The most common childhood tumors are leukemia, brain, and spinal cord tumors, neuroblastoma, retinoblastoma, bone cancer, Wilms tumor, lymphoma, etc. When it comes to digestive tract cancer, surgical gastroenterologists often see hepatoblastoma and pancreas blastoma in children.

1. Hepatoblastoma: Malignant liver cancer in young people Hepatoblastoma is a type of liver cancer found in infants, toddlers, and children. GI surgeons have noted that hepatoblastoma does not usually spread to other parts of the body.

Although the exact cause of the disease is unknown, experts pinpoint genetics. Beckwith-Wiedemann syndrome, familial adenomatous polyposis, glycogen storage disease, and Aicardi syndrome increase the risk of hepatoblastoma in young children. If a child is born with low weight, this can affect the risk of developing the disease.

Are there any symptoms of hepatoblastoma?

Symptoms of hepatoblastoma vary depending on the size of the tumor. But, the following symptoms should be looked for:

A. Abdominal lump/swelling

b. Enlargement of veins in the abdominal area

C. Abdominal pain

d. Difficulty eating and loss of appetite

E. Fatigue and unexplained weight loss

F. Nausea and vomiting

G. Fever

h. Jaundice

I. Itchy skin

 A doctor can diagnose the disease after physical examination, blood tests, ultrasound, tumor biopsy, CT, and MRI. A patient may need to undergo liver resection, chemotherapy, and radiation therapy to treat hepatoblastoma. After treatment, regular check-ups are essential.

2. Pancreas to pancreas blastoma: A rare pancreatic malignancy in children

Malignant tumors of the pancreas are different in children than in adults. Moreover, they have better clinical outcomes in the younger population. Surgical gastroenterologists, oncologists, and other health professionals have seen Pancreas to blastoma almost only in young children of, the range: up to 9 years.

Pancreas also Blas a  Mato blastoma, pancreatic blastoma, or infantile-type pancreatic cancer is the most common type of pancreatic tumor in younger children. It accounts for less than 0.2% of childhood cancer-related deaths in children. It means that early detection and timely medical treatment can help the child fight the disease.

What are the symptoms of the pancreas to blastoma?

Although the disease may be asymptomatic, parents and primary caregivers of the child should look for the following symptoms:

1. Abdominal pain and swelling

2. Fatigue and lethargy

3. Anorexia and weight loss

4. Diarrhea

5. Nausea and vomiting

Pan to ocrea screen to blastoma affects male children in the Asian population. Doctors believe that congenital cases of the disease have some connection with Beckwith-Wiedemann syndrome.

A surgical gastroenterologist will recommend tests: sonography, CT, MRI, etc. to diagnose pancreatic to blastoma. After a successful diagnosis, the young patient may need surgical resection of the pancreas to remove the tumor.

Treatment, care, and support are essential

Childhood cancer can affect a young patient. In immediate medical care, the emotional support of a counselor or support group is essential to help the child and family members. To fight against the terrible disease, children must undergo regular medical check-ups. Too, we need more awareness about childhood cancer, better medical infrastructure, and better public health strategies so that we do not lose our future generation.