Rare ‘Tree man Syndrome‘ Returns to Haunt Bangladeshi Man, Affects Young Girl
dhaka, Bangladesh – A Bangladeshi man battling the exceptionally rare and debilitating genetic disorder epidermodysplasia verruciformis, known as “tree man syndrome,” has been readmitted to hospital as the condition worsens despite previous treatment.The case highlights the agonizing reality of this incurable disease, wich causes bark-like growths to spread across the skin, and has also surfaced in a young Bangladeshi girl.
The former rickshaw driver, identified as Mr.Bajandar, initially gained international attention after doctors successfully removed 11lbs of growths in 2017.He expressed hope at the time that “the curse won’t return again.” However, he was readmitted in January after the condition resurfaced, with some growths now several inches long. Driven to desperation by the pain, Mr. Bajandar has pleaded with doctors to amputate his hands. “I cannot bear the pain anymore. I can’t sleep at night. I asked the doctors to cut off my hands so I can at least get some relief,” he told AFP. His mother, Amina Bibi, stated, “At least he will be free of pain. It’s a hellish condition.”
Epidermodysplasia verruciformis is an extremely rare genetic condition, with estimates of those affected globally ranging from a dozen to around 200.
Another young patient, known only as Muktamoni, is suffering from the same disease. Local reports indicate her upper body has been severely affected, with the right side of her chest and hand covered in brown, bark-like growths. despite the disease having spread throughout her body, the left side of her chest remains unaffected. Her right hand is also severely impacted, appearing curled and unusable due to the uncontrolled growth.
