LETTERS
bipeniden, increased
3 mg/day. The dose of haloperidol to 27 mg/day and propeniciazine
over
the next
trunk
gradually
ion
of the
4 weeks.
Within
developed
body
and
the following
a peculiar
backward
week,
position,
axial
rotation.
rarely reported in treatment,
was gradually to 225 mg/day with The
Mr.
A’s
side flex-
patient
was
considered to be suffering from the Pisa syndrome, since he fulfilled the criteria for tardive dystonia developed by Burke et al. (2) and showed the typical posture of this syndrome (1) without any other dystonic reactions.
The
propeniciazine
was
first
discontinued,
and
then
halopenidol was decreased to I 8 mg/day over 4 weeks, but without any noticeable improvement. We then tried agents reported to improve tardive dystonia, such as prometha-
zinc,
amantadine,
tiapnide,
carbamazepine,
lene sodium. 2 weeks with antipsychotic
Each of these was no benefit. Finally, from haloperidol,
I 8 mg/ day.
From
that
gradually improved within I week. The several months.
We changed son. ing
There the
Pisa
time
on,
agent
no report
syndrome.
of selective
The
affinity
non-D2 receptor sites For example, blockade idol exhibits in dystonia
with
for
rcarecep-
in in vitro radioreceptor activity of habopenidol
at
may be responsible for the syndrome. of the sigma receptor, which haboper-
a high
affinity,
is considered
to play
a role
(5).
REFERENCES 1. Ekbom K, Lindholm H, Ljungberg L: New dystonic syndrome associated with butyrophenon therapy. Z Neurol 1972; 202:94-
I03
caused
by antipsychotic
3. Yassa R, Nastase pleurothotonus): Psychiatry
I 990;
J, Marsden late-onset
drugs.
C, Cvejic prevalence
Neurology
CD, Lang AE, Gollomp and persistent dystonia 1982;
32:1335-1
J, Laberge G: The Pisa syndrome in a psychogeriatic population.
346
(or Biol
29:942-945
4.
Richelson E, Nelson A: Antagonism by neuroleptics of neurotransmitter receptors of normal human brain in vitro. Eur J Pharmacol 1984; 103:197-205 S. Walker JM, Matsumoto RR, Bowen WD, Gans DL, Jones KD, Walker FO: Evidence for a role of haboperidol-sensitive sigma‘opiate’ receptors in the motor effects of antipsychotic drugs. Neurology 1988; 38:961-965 EIJI SUZUKI, SHIGENOBU KANBA, MASASHI NIBUYA, FUTOSHI SHINTANI, NORIHISA KINOSHITA, GOHEI YAGI, MASAHIRO ASAI, Tokyo,
Rare
Presentation
of Tardive
SIR: Severe presentations quently disabling because movements, severe tardive
movements. ing irregular
Am
J
Respiratory respiratory
Psychiatry
Ms.
1 49:8,
M.D. M.D. M.D. M.D. M.D. M.D. M.D. Japan
Dyskinesia of tardive dyskinesia ( 1 ) are freof difficulties in masticatory akathisia, or limb and finger
or swallowing dyskinesias rates or grunting noises
August
1992
A had
been
treated
severe
presentation
woman with personality
for several
years
of
a diagnosis disorder ac-
with
tency neuroleptics, probably to contain agitation ety unresponsive to benzodiazepines. Persistent kinesia was diagnosed according to Schooler criteria (3) using the Rockland Simpson scale dyskinesia (4). Ms. A’s total score was 48.
high and
tardive
poanxi-
dys-
and Kane for tardive
of gait.
These
signs
were
associated
with
a continu-
typical tardive dyskinesia patterns, disappearing only during sleep and worsening with anxiety, and its continuous occurrence affected severely the patient’s speech and ability
to fall asleep. Awareness of this symptom was higher than for the other symptoms, maybe because of the auditory feedback. During 2 years of illness, severity was reported to decrease if neuroleptic doses were increased and to worsen upon decrease or withdrawal. The severity also increased if anticholinergics
stable drawal
2. Burke RE, Fahn S, Jankovic S, Ilson J: Tardive dystonia:
and
rhythmical, clearly involuntary vocal emission, like a cry, the origin of which seemed to be laryngeal, defined by the patient as “illness of the cry.” The vocal emission (together with other signs) followed
causD2
of rare
often irrelevant in these cases
ous,
disappeared over the next
D2 antagonists
a case
tardive dyskinesia in a 57-year-old of dysthymic disorder and histrionic cording to DSM-III-R.
malities
symptoms
for the following
(1). We observed
strategies, and ineffective
EDITOR
Upon admission Ms. A showed chewing movements, choreoathetoid movements of the tongue, blepharospasmus, finger movements, akathisia, and bordosis with abnor-
more than the patient’s to pimozide,
of pimozide
tors is higher than that of haloperidol assay (4). This suggested that the
dantro-
for
the dystonic
and almost completely symptoms did not recur
the antipsychotic
has been
and
prescribed we changed 18 mg/day,
(2). Therapeutic are more difficult
TO THE
produchave been
were
used.
In the last 6 months
severity
was
with Ms. A taking cbothiapine, 40 mg/day. Withfrom medication induced a significant worsening of
vocal emission and other symptoms. Neurological examination and nuclear magnetic resonance imaging excluded an olivopontocerebellar syndrome, which was considered in differential diagnosis, as well as other neurological conditions possibly related to the vocal emission and other involuntary movements. After 1 week of treatment with clonazepam. 8 mg/day,
most bances,
symptoms and
the
decreased, vocal
38), which remained 1 -month observation
except
emission
(total
unchanged period.
lordosis,
gait
distur-
Simpson
scale
score=
throughout
the following
The similarity of our patient’s symptoms with Tourettes’s disorder is worth noting. Our observations seem to be quite similar to cases of tardive Tourette’s disorder reported in the literature (5).
REFERENCES 1. Gardos G, Cole OJ, Salomon M, Schniebolk 5: Clinical forms of severe tardive dyskinesia. Am J Psychiatry 1987; 144:895-902 2. Casey DE: Tardive dyskinesia, in Psychopharmacology: The Third Generation of Progress. Edited by Meltzer HY. New York, Raven Press, 1987 3. Schooler NR, Kane JM: Research diagnosis for tardive dyskinesia. Arch Gen Psychiatry 1982; 39:486-487 4. Simpson GM, Lee JH, Zoubok B, Gardos G: A rating scale for tardive dyskinesia. Psychopharmacology I 979; 64:171-179 S. Shapiro AK, Shapiro E: Tic disorders, in Comprehensive Textbook of Psychiatry, vol V. Edited by Kaplan HI, Sadock BJ. Baltimore,
Williams
& Wilkins,
1989
R. CAVALLARO, E. SMERALDI, Milan,
M.D. M.D. Italy
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