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P

hototherapy

with

PUVA: V

ersatility

and

efficacy

in

dermatoses

R

ev

A

ssoc

M

ed

B

ras

2017; 63(5):393-396

393

SPECIAL ISSUE

Phototherapy with PUVA: Versatility and efficacy in dermatoses

T

atiana

F

erreira

F

rança

1

*, A

lessandra

V

ieira

D

iniz

1

, I

vanete

L

opes

da

S

ilva

1

, R

afaella

R

êllo

P

into

C

oelho

C

arvalho

1

,

V

anessa

K

nauf

L

opes

1

, V

irgínia

V

inha

Z

anuncio

2

1

Medical Student, Universidade Federal de Viçosa (UFV), Viçosa, MG, Brazil

2

Assistant Professor of Dermatology, Department of Medicine and Nursing, UFV, Viçosa, MG, Brazil

Study conducted at Department of Medicine and Nursing, Universidade Federal de Viçosa (UFV), Viçosa, MG, Brazil

Article received:

11/4/2016

Accepted for publication:

11/20/2016

*Correspondence:

Address: Rua Feijó Bhering, 53, apto. 604

Viçosa, MG – Brazil

Postal code: 36570-000

tatif.franca@hotmail.com http://dx.doi.org/10.1590/1806-9282.63.05.393

I

ntroduction

Phototherapy is used in the treatment of several derma-

toses, many with high prevalence and chronic progres-

sion.

1,2

Its classification is made according to the type of

irradiation: ultraviolet A (UVA – between 320 and 400 nm

wavelength) or ultraviolet B (UVB – between 290 and 320

nm).

1

The range of UVB between 311-312 nm is called

narrow-band.

The immunological basis of phototherapy is the ac-

tivation of immune-modulating cascades caused by the

absorption of UV rays by chromophores of the skin. Cell

membrane and DNA damage

3

occur due to photochem-

ical reactions that have anti-inflammatory, immunosup-

pressive and antiproliferative effects.

1,4

In order to determine the time and intensity of the

sessions, a minimal erythematous dose (DEM), which is

the minimum energy required to produce a uniform ery-

thematous response within 24 hours, is calculated. Treat-

ment is started with 75 to 90% of this dose. The energy is

gradually increased to minimize adverse reactions and

potentiate the treatment.

1

PUVA treatment uses oral or topical psoralen followed

by exposure to UVA irradiation.

4

Psoralens are tricyclic

furocoumarins derived from plants and activated by UV

rays.

4,5

The PUVA procedure with oral psoralens should

be preceded by ophthalmologic evaluation and serum

dosage of ALT, AST, gamma-glutamyltransferase (gamma

GT), alkaline phosphatase, urea, creatinine, BHCG for

women of childbearing age and antinuclear antibodies

(ANA) to detect potential sensitivity to R-UVA. Topical

PUVA, in turn, is indicated primarily for patients with

hepatic or gastrointestinal dysfunction, cataract, drug

interactions, and for children.

4,5

The absolute contraindications for PUVA are xero-

derma pigmentosum, some genodermatoses, systemic

lupus erythematosus, dermatomyositis, previous history

of melanoma and trichothiodystrophy. Relative contrain-

dications include age less than 10 years, previous or current

history of non-melanoma skin cancer, immunosuppressive

treatment, gestation, cataracts, severe hepatic dysfunction,

and history of systemic malignant tumors.

2

Adverse effects include increased risk of melanoma

and non-melanoma skin cancer, gastrointestinal chang-

es, erythema, burns and pruritus. There may be conjunc-

tival changes and early cataract, justifying ocular protec-

tion with sunglasses for at least eight hours after

ingestion of psoralens. As a late manifestation there is

photoaging.

1,4,6

Medical supervision and periodic labora-

tory evaluation are fundamental, as well as avoiding sun

exposure with the use of physical and chemical barriers

during treatment.

2

This article aims to report three clinical cases, one of

psoriasis, one of vitiligo and one of pityriasis alba, treated

with PUVA with excellent response and, thus, show the

diversity of dermatoses that can be treated with this the-

rapeutic option. All the patients authorized in writing the

use of their images as illustration of the cases by signing

Free and Informed Consent Terms (FIC) forms.