Jérôme Frenchise
02-01-2016, 07:25 AM
http://www.independent.co.uk/news/world/asia/man-with-rare-skin-disease-to-receive-specialist-treatment-a6843726.html
Bangladeshi man with rare condition that makes skin 'look like wood' to receive specialist treatment
http://static.independent.co.uk/s3fs-public/styles/story_large/public/thumbnails/image/2016/01/30/16/Abul-Bajandar-2.jpg
Abul Bajandar has been suffering from the condition for more than six years Suvra Kanti Das/ZUMA Wire/REX Shutterstock
A Bangladeshi man who has been suffering for years from a rare skin disease is set to recieve specialist treatment.
Abul Bajandar, 25, from Khulna in the south west of the country, suffers from Epidermodysplasia Verruciformis, a skin condition causing extreme growths. The growths caused by the disease have been likened to that of tree bark and roots.
Mr Bajandar was forced to quit his job as a rickshaw driver after the growths became problematic.
“Initially, I thought that they’re harmless," said Mr Bajandar to AFP news agency. "But slowly I lost all my ability to work. There are now dozens of two-to-three-inch roots in both my hands. And there are some small ones in my legs.”
http://static.independent.co.uk/s3fs-public/styles/story_medium/public/thumbnails/image/2016/01/30/16/Abul-Bajandar-1.jpg
Dr Lal Sen said to The Independent: "We have decided to have some investigations including biopsy. After that we will improve his general condition and then slowly we we will go for series of surgical procedures. It will take few weeks to prepare him. All the treatment will be in our unit."
Dr Lal Sen added that the treatment would be undertaken at the expense of the government.
Mr Bajandar was previously being treated in the burns unit of Gazi Medical College Hospital in Khulna.
http://static.independent.co.uk/s3fs-public/styles/story_medium/public/thumbnails/image/2016/01/30/16/Abul-Bajandar-3.jpg
Epidermodysplasia Verruciformis is a rare hereditary condition, often causing skin tumours and chracterised by an "unusual susceptibility to infection with specific types of human papillomavirus" according to the US National Library of Medicine.
Bangladeshi man with rare condition that makes skin 'look like wood' to receive specialist treatment
http://static.independent.co.uk/s3fs-public/styles/story_large/public/thumbnails/image/2016/01/30/16/Abul-Bajandar-2.jpg
Abul Bajandar has been suffering from the condition for more than six years Suvra Kanti Das/ZUMA Wire/REX Shutterstock
A Bangladeshi man who has been suffering for years from a rare skin disease is set to recieve specialist treatment.
Abul Bajandar, 25, from Khulna in the south west of the country, suffers from Epidermodysplasia Verruciformis, a skin condition causing extreme growths. The growths caused by the disease have been likened to that of tree bark and roots.
Mr Bajandar was forced to quit his job as a rickshaw driver after the growths became problematic.
“Initially, I thought that they’re harmless," said Mr Bajandar to AFP news agency. "But slowly I lost all my ability to work. There are now dozens of two-to-three-inch roots in both my hands. And there are some small ones in my legs.”
http://static.independent.co.uk/s3fs-public/styles/story_medium/public/thumbnails/image/2016/01/30/16/Abul-Bajandar-1.jpg
Dr Lal Sen said to The Independent: "We have decided to have some investigations including biopsy. After that we will improve his general condition and then slowly we we will go for series of surgical procedures. It will take few weeks to prepare him. All the treatment will be in our unit."
Dr Lal Sen added that the treatment would be undertaken at the expense of the government.
Mr Bajandar was previously being treated in the burns unit of Gazi Medical College Hospital in Khulna.
http://static.independent.co.uk/s3fs-public/styles/story_medium/public/thumbnails/image/2016/01/30/16/Abul-Bajandar-3.jpg
Epidermodysplasia Verruciformis is a rare hereditary condition, often causing skin tumours and chracterised by an "unusual susceptibility to infection with specific types of human papillomavirus" according to the US National Library of Medicine.