As a remarkable medical achievement, doctors have successfully removed a giant tumor in 5 parts of the face of a 3-year-old child with good recovery ability. The pain took away her jaw and jaw, posing a significant challenge, but skilled medical professionals triumphed over the adversity.
The team demonstrated extraordinary expertise as they delicately approached the complex process. Removing excess skin growth requires precision and care, and the sensitive skin on a child’s face.
Your resilience has shown remarkable courage throughout, demonstrating the strength that often comes in the face of adversity. Her work is a testament to the resilience of the human spirit, especially when faced with difficult health challenges.
This not only highlights the capabilities of modern medicine but also emphasizes the importance of early detection and treatment of medical cases. Successful removal of the tumor not only restores the child’s physical health, but also promises her a brighter, tumor-free life.
The medical community is abuzz with reports of this extraordinary case, which sheds light on the complexity of pediatric surgery and the concomitant advances in medical technology.
This achievement serves as an inspiration to medical professionals around the world and recognizes the significance of collaborative efforts to overcome medical challenges.
Accordingly, the removal of a 5-point tumor on the 3-year-old child’s face is considered a ray of hope and recovery. It highlights the incredible advances that have been made in the medical field and promotes new focuses on early detection and advanced treatments.
As this remarkable story captures everyone’s attention, it serves as a reminder that with determination and cutting-edge medical expertise, even the most difficult medical challenges can be overcome. through
Once there was a 2.2kg tumor under her chin. It was thought that the life of 3-year-old Brazilian girl Melyssa Delgado Braga would no longer have hope. However, thanks to a surgery, my life has turned a new page.
A few months ago, doctors in Louisiana, USA performed a tumor removal surgery on a 3-year-old Brazilian girl, after her parents posted information online and asked for help. everybody.
After a surgery lasting more than 8 hours, her tumor was removed. Melyssa Delgado Braga also recovered quickly and led a normal life. However, before the surgery was performed, few people knew how tumultuous her life had been.
Little Melyssa’s journey to America began when Celso Palmieri Jr., an assistant professor in the department of maxillofacial orthopedic surgery at Louisiana State University Health Sciences Center, read a post on a blog. Brazilian newspaper page while reviewing publications published in his home country. By chance, this assistant saw a post from baby Melyssa’s parents. Her parents are desperate, hoping to find a benefactor or hospital to help remove her tumor in the US.
After an hour of searching on social networks, Dr. Ghali found this parent’s contact information. However, they only speak Portuguese.
Ghali, president of the Louisiana State University Health Association, said he could help Melyssa. However, before reaching out to her family in Brazil, he wanted to ensure that there would be a safe and affordable place for them to live in the United States.
Ghali turned to Willis-Knighton Health System in Shreveport, a nonprofit health care organization that specializes in housing patients with rare surgeries and foreigners. The staff here said they agreed to provide accommodation for Melyssa’s family at an affordable price.
A month later, Melyssa flew to America for surgery. Ghali diagnosed her with myxoma – a very rare malignant tumor.
“This is a benign tumor, with no cancer cells, luckily. However, this tumor has covered her entire jaw and pressed on her tongue. It is difficult for her to eat and drink normally.” Normally, if left like that, Melyssa will become malnourished.”
Lisa Balin, director of Louisiana State University’s medical center, said the cause of myxoma is unknown. This disease is more common in women than men. About 10% of people with myxoma have genetics. Usually, it also occurs in young patients.
Without surgery, Melyssa will need a tube to be able to digest food and after just a month, she will have difficulty breathing. “Patients will die slowly from malnutrition and asphyxiation.”
“I am truly grateful for everything the doctors did for my daughter during a month of surgery and treatment,” her father said. Now, Melyssa has a normal life, her tongue can function freely and her physical condition is stable like many of her peers.
“Reading about the girl’s story, I realized that our department could help her, specifically Dr. Ghali and his team. I have seen doctors help many people. That’s why I decided to help her.” Take a picture of baby Melyssa and send it to him,” Palmieri recounted the story.