The man was the victim of a rare disease: doctors barely have time to do surgery, photos

Мужчина стал жертвой редкой болезни: врачи с трудом успевают делать операции, фото

On is impossible to watch without tears: despite the efforts of modern medicine, the man stubbornly turns into a tree

Patient from Bangladesh Abul Bajandas is one of the rarest, suffering from an exotic disease in which the skin is because of the huge number of warty growths, transformed into a conglomerate of like tree bark.

Мужчина стал жертвой редкой болезни: врачи с трудом успевают делать операции, фото

The poor creature because of its appearance earned the nickname “tree man”.

The disease, which literally absorbs a man called verruciformis epidermodysplasia.

26-year-old man first went to the doctors back in 2016. Then the doctors amputated more than five kilograms of malevolent growths from the body of Aboul Bandara.

Мужчина стал жертвой редкой болезни: врачи с трудом успевают делать операции, фото

Since that time, the patient underwent 25 such an operation and underwent long-term therapy. There was a period when doctors thought that they were able to achieve disease remission, but in may of 2018, the disease gave a new, hard relapse.

Abul Bazantar again came to the hospital, but soon left it to find another treatment. Alternative. Apparently the man managed to completely give up on traditional methods of treatment of the disease.

Мужчина стал жертвой редкой болезни: врачи с трудом успевают делать операции, фото

Illness forced him to return to the hospital on Sunday, January 20. Poor guy was exhausted and needed urgent assistance. Other treatment for himself, he was never found.

Due to the fact that the disease managed to reach status “running”, doctors will have to start all over again.

Plastic surgeon Dr. Samanta Lal sen said that the treatment will be started very soon. The doctor emphasized that doctors will have to conduct therapy from the beginning.

Мужчина стал жертвой редкой болезни: врачи с трудом успевают делать операции, фото

The Prime Minister promised that the man does not have to pay for treatment. How to escape, Baganda will be placed in an expensive house with his wife and daughter.

Previously, we reported that in Belgium, live brother and sister suffering from a rare genetic disease which causes premature aging or progeria syndrome Hutchinson-Gilford. People with this disease do not live long. To date, the record is the lifetime in 26 years.

In the world now live only 155 people with the same diagnosis. When the Vim and Goteliv Vandervert first child was born — Michelle, the doctors told them that the birth of their second child with the same diagnosis impossible. However, contrary to the theory of probability, their daughter, amber, at the age of seven weeks revealed the same disease.

Recall, the twin-parasite “devoured” baby, doctors performed a unique operation.

As reported Politeka, doctors the United States conducted the complex surgery, which was hidden for five months.

Also Politeka wrote that Komorowski warned parents about a fatal mistake.

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