Patching
up the patches
Children
suffering from leukoderma are getting a new lease of life at the
Lady Ridgeway Hospital. Kumudini Hettiarachchi reports on this medical
breakthrough
A little child with a blob of white cream daubed on her skin is
seated without a murmur while people around her bustle about scraping
behind her ear. Look closely and the cream is on a stark white patch
of skin.
The
girl is a sufferer of leukoderma or vitiligo which creates stigma
and ostracism. Derogatorily dubbed kabara, this skin disease linked
to one’s pigmentation going awry, creates much heartache and
sorrow because most people dare not touch the person due to many
widely-held misconceptions
One such entrenched belief among men, women and children is that
leukoderma is incurable. If you have it, you’ve got to live
with it, is the general thinking. But as soon as one steps into
the skin clinic of the Lady Ridgeway Hospital for Children, that
thinking changes drastically.
Right before one’s eyes, a procedure is being performed under
local anaesthesia to correct the problem and in the case of another
child one sees the white patches getting covered by brown dots which
spread gradually, bringing back the normal pigmentation of the skin.
“Normal skin is taken from a place not visible directly and
then grafted to a patch of vitiligo,” says Dr. Jayamini Seneviratne,
LRH’s Consultant Dermatologist, explaining that the pigment
then starts spreading after two-three weeks.
Calling
it a good, rapid response, he stresses, “The pigmentation
is identical to the surrounding skin. This type of grafting is very
effective if the disease is stable and no new lesions have occurred
within three months.” The procedure takes from anything between
half-an-hour to three hours and in recent times the clinic has attended
to about 100 children ranging from babies to teens.
Detailing other treatment for the same condition, Dr. Seneviratne
said it should be on a case-by-case basis. “It has to be very
individualistic and include use of sunscreen for extensive lesions
which could be susceptible to sunburn, various creams and lotions,
a special type of light therapy, cover-up cosmetics and surgical
treatment using the patient’s own melanocytes. In a few rare
cases we carry out de-pigmentation of the remaining brown patches
to bring about extensive discolouration.”
The Sunday Times learns that some people, not of the medical profession,
try out various methods of ineffective treatment including scraping
the affected section of the body with a sharp three-pronged instrument,
causing immense suffering to these children.
“Come
early,” Dr. Seneviratne urges parents offering them hope.
“Come as soon as you see the first signs.”
Leukoderma:
What is it?
The main pigment in the human skin is melanin found in the cells
called melanocytes, says Dr. Seneviratne giving a picture of the
human skin.
Melanin is synthesized in the human body using a number of enzymes
and is stored and transferred to other cells, giving the colour
or pigment of each individual’s skin.
Any
problem in the whole process, either of synthesis or transfer can
lead to a marked pigmentary dilution known as albinism and related
disorders. When the melanocytes are destroyed due to acquired causes
there is patchy pigmentary loss known as vitiligo or leukoderma.
“The commonest way this happens is when one’s own immune
system destroys the melanocytes. This condition is called auto-immunity.
While the other causes could be neuro-chemical or self-destructive,
in a rare case it could be hereditary,” he says. Leukoderma
can be categorised into generalized or acrofacial, segmental, focal
and universal.
In vitiligo there is pigmentary loss or white areas and light brown
areas, he says, and spontaneous re-pigmentation within the white
areas. There can be associated white hairs but the texture of the
skin is normal. On rare occasions vitiligo can be associated with
other diseases including diabetes, thyroid disease and even rare
conditions involving the eye and the brain. “The onset of
the disease can be at any age, childhood to adulthood. It is a polygenic
disorder with some family members being affected.” |