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For years, a man from Bangladesh has been living with the syndrome of "tree man".
Abul Bajandar's hands and feet developed "roots" that prevented him from feeding, moving, working, or wearing normal clothes.
Three years ago, the 28-year-old father became viral while he was undergoing a series of invasive surgeries to remove "bark" from his hands and feet.
Bajandar lived with what had been identified as verruciform epidermodysplasia (EV), a rare skin condition, for more than 20 years.
The symptoms of the disease are extreme growths that look like warts all over the body, caused by a defect in the immune system. It increases susceptibility to HPV, or human papillomavirus, which often leads to infection, skin lesions and increased risk of melanoma.
According to the World Health Organization, HPV is spread worldwide, with over 100 different types existing. The epidermodysplasia verruciforme is different in that it prevents the victims from fighting against certain types of HPV.
The "Tree Man" syndrome is so rare that only 200 cases have been reported worldwide.
The doctors told CNN that after Bajandar's 25 unsuccessful operations, he refused to return for further treatment.
"It's a complicated affair and we're progressing, but he's gone home, I asked him many times to come back, but he did not do it," Dr. Samanta said. Lal Sen, coordinator at the Burns and Plastic Surgery Unit. from the hospital and medical college of Dhaka, told CNN.
There is no cure for EV, but cryotherapy, topical creams and retinoids may be prescribed to eliminate growths.
"I want to live like a normal person," Bajandar told CNN. "I just want to be able to hold my daughter properly and hug her."
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