Dear Editor,
Adult-onset atopic
dermatitis (AOAD) (onset >18 years) is a subgroup of atopic dermatitis (AD).
This subgroup has been mentioned by Bannister and Freeman from Australia1.
It may have different morphologic variants. Apart
from the most
typical flexural localization and eczematous pattern
in adults, patients may also have a nonflexural distribution and other morphologic variants
such as nummular or prurigo-like pattern2.
The Hannifin and Rajka criteria can be used to diagnose AOAD3. AD is
occasionally associated with vitiligo, and patients with vitiligo, especially
early onset may appear to have increased risk of AD4.
We present a rare
case with late onset atopic dermatitis and vitiligo. A 16 year old boy
suffering from itchy lesions and dryness on his whole body, especially on
flexural distributions for 6 months admitted to our out-patient policlinic. He
also complained depigmented lesions. No personal history of atopy. His mother
has an allergic rhinitis for many years.
Dermatologic
examination of the patient revealed pruritic dry skin, pilar keratosis, and
symmetric lichenified flexural eczema. He has a facial erythema, orbital
darkness and Dennie-Morgan folds (Figure 1).
Potassium hydroxide
preperations were negative. Histopathologic examination of the lesions showed
the findings of chronic dermatitis. The diagnosis of atopic dermatitis was made
based on Hanifin-Rajka criteria.
He has also
symmetric depigmented lesions on the popliteal skin area. Wood lamp examination
of these lesions revealed blue-white light areas with sharp margins.
Haematologic and
urine analysis, including IgE, ANA and antithyroid antibodies were in normal range.
Atopic dermatitis is a chronic or chronic relapsing,
the classic morphology and location of which differs
depending on age, and which is usually associated with severe
pruritus. AD is
a common
skin disease, both in childhood and adolescence and in adults5. The
term AOAD
(onset >18 years) was introduced by Bannister and Freeman1. The
onset age
of the disease in our case was 16. Because of that,
our case is not an AOAD. However,
his diagnosis may be accepted as a late-onset atopic dermatitis.
There is lack of diagnostic criteria useful in both
children and adults. Therefore understanding the natural
history of AD
is complicated. The UK working party criteria may not perform well
among adults6. Ozkaya1 reported that there is no problem
in detecting early-onset AD
according to The UK working criteria, but
approximately one fourth of patients could not be given the
diagnosis of AOAD
according to this in its current form. The criteria of Hanifin and Rajka
have been considered as a gold standard for AD diagnosis for the last 20 years,
and this criteria
was used in the diagnosis of our case. A diagnostic difficulty may arise when
the onset
occurs after the adolescence or later, as in these
cases the clinical pattern may be atypical. However it may
still present with flexural dermatitis3. Our case had a typical
typical flexural distribution and lichenified eczematous pattern.
AD
may be associated with specific subsets of vitiligo, and may indicate poor prognostic
value for vitiligo. The mechanisms of association between AD and
vitiligo are
yet unknown. Patients with vitiligo, especially early onset, appear to have
increased risk of AD4.
The onset time was almost the same for both diseases in our case. However, while
our case has a late onset time for AD,
but early onset for vitiligo.
Further studies are needed to explain the association
between atopic dermatitis and vitiligo, and common
disease mechanisms for both diseases.
Subjects | Health Care Administration |
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Journal Section | Letters to the Editor |
Authors | |
Publication Date | May 16, 2017 |
Acceptance Date | November 18, 2016 |
Published in Issue | Year 2017Volume: 39 Issue: 2 |