Abdul Bajander

Abdul Bajander

Bangladeshi man with epidermodysplasia verruciformis
Country: Bangladesh

Content:
  1. Biography of Abdul Bajander
  2. The Rare Disease
  3. The Documentary and Surgery
  4. Local Fame

Biography of Abdul Bajander

A Bangladeshi Man with Verruciform Epidermodysplasia

Abdul Bajander, a 25-year-old man from Bangladesh, has suffered from a disease that only five people in the world have. He has gained the nickname 'Tree Man' due to the gigantic bark-like growths protruding from his hands and feet. After a successful surgery to remove these abnormal wart-like formations, Bajander was able to eat without assistance for the first time in many years.

Abdul Bajander

The Rare Disease

Abdul is a victim of epidermodysplasia verruciformis, an extremely rare genetic disorder that causes the massive development of warts of various sizes. This condition is also known as Lewandowsky-Lutz dysplasia or 'Tree Man' syndrome. Bajander was forced to quit his job as a rickshaw driver due to his debilitating condition. He expressed, "Sometimes, I doubt why the Almighty has burdened me with such a terrible disease. My fate scares me."

Abdul Bajander

The Documentary and Surgery

Bajander's story was featured in a recent documentary film on Barcroft TV. It was revealed that he underwent a three-and-a-half-hour surgery, performed by nine doctors. Prior to Bajander, no cases of verruciform epidermodysplasia had been reported in Bangladesh. Reports suggest that worldwide, only five individuals have become victims of the 'Tree Man' syndrome. Dr. Samanta Lal Sen, the plastic, reconstructive, and cosmetic surgeon who operated on Abdul, stated, "In my entire life, I have never come across a patient like him."

Abdul Bajander

Local Fame

Bajander has become somewhat of a celebrity in his hometown of Khulna. Hundreds of strangers have visited him in the hospital to see the extraordinary man.

Abdul Bajander

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