Rev. Inst. Med. trop. São Paulo 26(5) :259-266, setentbro-otttubro. 1984
TREATMENT OF DERMAL GYSTICERCOSIS WITH
PRAZIQUANTEL
(").
A
NEW CESTOCIDAL AGENTMiroslau Constante BARANSKI (t)
SIJMMARY
Twenty adult patients presenting dermal cysticercosis without cerebral or
ocular involvement were treated with praziquantel. The
first
eleven cases receiv-ed 60 rng,¡hglday and the last nine cases B0mglkg/d4y.
rn
both
groups thedaily dose was
split into
three oral intakes4 to
6 hours apart andthe
drugadministration lasted
for
6 consecutivedays.
The latter groupof
patients alsogot dexamethasone,
3
mg daily,from
one day beforeuntil
four days after thetreatment period
with
praziquantel. The drug proved.to
be
r00vo efficacious as demonstrated histopatholqgically by the death of the cysticerciof
Taeniaso-lium
(Çysticercus cellulosae)in
serial biopsies takenfrom
the 2nd week onaft'er the end of treatment, as well as clinically by the steady disappearence of the dermal nodules during the
6
months following thetherapy.
Tolerance oî praziquantel was good as the incidence and severityof
side-effects were not Íe-levant. The drug safety was confi¡meci through laboratory tests which failed. todetect any abnor'rrral findings related
to
the
hematopoietic,liver
and kidney functions.UDC 6t6.995.1
INTRODUCTION
Praziquantel,
an
heterocyclic isoquinoline derivative, is a new synthetic cornpound highlyactive
in
experimental and human infections causedby
cestodes 1,8,72,73.74.It
acts against Cysticærcus bovis,the
larval stageof
Taenia saginata, in naturally infected calves as well asa,gainst Cysticercus cellulosae, the larval stage of Taenia solium, in naturally infected pigs2,s,rs. Extensive pharmacological
and
toxicological studies had demonstrated the tolerance andsa-fety
of
praziquantelin all
tested animalspe-cies, including controlled trials involving health volunteers 4'7.
This clinical trial was carried out with the
aim of assessing the efficacy of this new cesto-cidal agent in the treatment
of
human dermal cysticercosis causedby
Cysticercus cellulosae.Trial subjecús and Methods
All twenty patients were treated at the De-partment
of
Infectious and Parasitic Diseases, Medicai School, Federal Universityof
Paraná,Curitiba,
B¡azil.
Thirteen cases were admittedto
the
Hospital duringthe
treatment perÍod whereas seven cases were treatedat
the
out-patient clinic. Praziquantel was administered
per os for six consecutive days. The daily dose was split into three intakes 4 to 6 hours apart. The
first
11 patients received 60 mg,4<g,/day andthe last nine patients half that dose. This
se-cond group also received 1 mg
of
dexametha-sone t.i.d. starting one dayprior
to theprazi-quantel
intake.
The corticoid administrationwas maintained until four days after finishing
the
treatmentwith
praziquantei.The
daily dose of dexamethasone wâs gradttallydecreas-(.)
(t) The CISTICID late Head _ MeIcK P¡ofessor,S.A.
raná, Curitiba, Brazil
Indúst¡ias Qufmicas
Infectious and Parasitic Diseases; Faculdade de Medicina, Universidade Federal do
BARANSKI, M. C. - Treatment of dermal cystlcercosis with praziquantel. .4, ne$' cestocidal agent. Rey. Insú. Med. trop,
São Paulo 26:259-266, 1984.
Numbet of de¡mal nodules Before treatment
4to 9
No.
rAD!DI
Dis¿ribution of dermal nodules
10 to 19
20 to 29
-iJ Number of patients
30 or more
1 month
No.
Number of demal nodules
30.0
Total (in 20 câses)
(o/o')
Minimum
10.0
Maximm
After t¡eatment
3 months
Reduction
Before treatment
TÁ.BLE II Therapeutical response
to
the drug administration, there was a singleremaining nodule and; one case initiâIlJ¡ with 25 had two nodules left. These remanent nodu_ les were smaller and had a harder consistency than at the begining but they were still painless and moveable. Comparing 60 ând 30 mg/kg/day
no statisticalþ significant difference was found. between the two doses at the 6th month after
therapy.
The biopsy taken two weeks after the end
of
treatment already revealeda
disintegratedcysticercus. Macroscopically one sees a shrunk gelatinous cream-like mass of soft consistency.
Looking through the microscope, the tegument
is
disruptedno
lor¡ger makingit
possible to identify its three layers. InsÍde the vesicle the262
6 months No.
?0.0
lst month
(o/o)
13.1
After treatment
3rd month
G7.60/o
scolex
is
detached from the collum and d.epri-ved of hooks and suckers. The dead parasite is surrounded by a conspicuous lymphoplasmocitÍc inflammatory reaction ,with eosinophils also
present Fig. 3.
One month after treatment the macro- and microscopic aspects are similar but the proces-ses of degeneration and reabsorption of the cys-ticercus are more advanced and signs
of
chro-nic
inflammatory andfibrotic
reactions startto appear Fig. 4.
The biopsy repeated
on the
third
monthfollowing the therapy shows the dead cysticer-cus reduced to a lenticular tuberculum of hard
consistency. Under the microscope one obser-6th month
85.90/o
BARANSKI, M. C. - Treatment of dermâl
São Paulo 26:259-266, 1984.
Meån nMber of dermal nodule6
cysticercosis tvith praziquantel. ,q, new cestocidal âgent. Rev. Inst. Meil. trop.
ves signs of chronic inflammation
-
fibroblastin
radial arrangement and giant cells t¡picalof
foreign body granuloma-
and fibrosis in-duced by the death of the parasite Fig. 5.In
the serum,prior
to
the treatment, the complernent fixation was positive in 14 patients (mean and standard deviation,7
:h 4.6 units)and the indirect hem4gglutination in 12 patients (mean and standard deviation, 1: 163
t
1: 159).In
six cases both reactions were negative. On the third month after therapy the complementfixation contìnued
to
be positivein
the same L4 casesbut
the mean value diminished to 1.1I
0.2units.
The indirect.hemagglutination became negativein
5 cases and its mean titerdecreased to 1.34
a
1;9, TaþleIII.
-45.9 %
After treatment
GRAPIIIC 1-REDUCTION OF DERMAL NODULES FOLLOWING
PRAZIAUANTEL ADMINISTRATION
Regarding the occurrence
of
adverse drug reactions, only eight cases reported untowardeffects. Abdominal pain or disconfort was the
most common complaint (in 3 cases) then
nau-sea (in 2) and vomiting, general malaise,
dizzi-ness, drowsiness, headache (in
1).
These symp-toms started during thefirst
3
daysof
drugintake and lasted
for
about 6 days. \¡/hilst 7patients treated with 60 mg/kg/day cornplained of side-effects, just 2 of those who received 30
mg/kg/day
had
cornplaints. However, therewas
no
statisticalþ significant
difference between the tolerance of both doses, Table IV.It
was found no abnormalitiesin
thelabo-ratof,y results indicative
of
toxic praziquantelupon ùhe hematopoietic lÍver and kidney func-tions.
B.ARANSKI, M. C, - Treatment of dermal cysticercosis v/ith praziquantel. Â new cestocidal agent. Rev. Inst. Med. trop. São Paulo 26t259-266. I98a.
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Il¡¡menolepíase nam com dose oral única de prazi quantel. Estudo de eficácia, tolerância e segurança.
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CHAVARRIA, M. & GONZÁLEZ, D. D. -
Praziquan-tel (Droncit) en el tratamiento de Ia cisticercosis
porcina. Esp. Vet. 1: 159-165, 19?8.
FLISSER, A.; PEREZ-MONTFORT, R,. & LARRAI.DE,
C. - The imunology of human cysticetcosis: a
re-view. Bull. W.H.O. 5?: 839-856, 1979.
FR,OHBERG, H. & SCHULZE SCHENCKING, M. -Toxicological profile of praziquantel, a new drug
against cestode and schistosome infections, as
com-pared to some othet schistosomicides. Drug Ees.31:
555-5'55, i981.
GALLIE, G. J. & SEWELL, M. M. H. - The efficacy
of praziquantel against the cysticerci of Ta.enia
sa-ginaf,a in câlv€s. Trop. Anim. HIth. Prod. l0: 36-88, 19?8.
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6.
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11
8.
t2
L4
Recebido para publicação eñ 3/4/L984.
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