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  • FapUNIFESP (SciELO)  (2)
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  • FapUNIFESP (SciELO)  (2)
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  • 1
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 2000
    In:  Arquivos de Neuro-Psiquiatria Vol. 58, No. 2B ( 2000-06), p. 522-530
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 58, No. 2B ( 2000-06), p. 522-530
    Abstract: Movement disorders have rarely been the result of psychiatric disturbances. Psychogenic dystonia is caracterized by inconsistent findings, a known precipitant factor, onset in legs, pain , multiple somatizations and incongruent association with other movement disorders. We report two patients with clinically established psychogenic dystonia. Patient 1: a female that presented sudden loss of strength in her four limbs; she developed feet dystonia, alternant laterocollis, generalized and irregular tremor, and limb hypertonia that disappeared with distraction; psychological examination showed severe depression, hypochondria and obsessive disorder. Patient 2: a female that presented with irregular limb tremors that disappeared with distraction and left foot dystonia nine years ago; she gradually lost her walk capacity; she complained pain in lumbar area and in her left limb, psychological examination showed infantile behaviour, low frustration tolerance, impulsivity and self-aggression. Their complementary exams showed no alterations and they had no reponse to specific pharmacological treatment. Dystonia is rarely psychogenic, but this etiology is suggested when clinical characteristics are inconsistent and incongrous with a classical disorder. It shoud be part of differential diagnosis when appears in association with other somatization or psychiatric disorders.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 2000
    detail.hit.zdb_id: 2053072-9
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  • 2
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 2000
    In:  Arquivos de Neuro-Psiquiatria Vol. 58, No. 2B ( 2000-06), p. 578-582
    In: Arquivos de Neuro-Psiquiatria, FapUNIFESP (SciELO), Vol. 58, No. 2B ( 2000-06), p. 578-582
    Abstract: Dementia is one of the manifestations of late syphilis and it is characterized by cognitive deterioration and behaviour disturbances. We report on a male patient with cognitive decline, behaviour disorder, hyperactivity, hallucinations, short-term memory and Argyll Robertson pupils due to neurosyphilis. Minimental state test (MST) was 16. Cerebrospinal fluid (CSF) protein concentration was 82 mg/dl, CSF-leucocyte count 128 cells/mm3 (98% mononuclear cells), CSF-VDRL 1:4, and CSF-T.pallidum haemaglutination assay 1:2560. MRI showed no cerebral alteration, but SPECT revealed left fronto-temporal hypocaptation. He received intravenous penicillin. MST done 3 months after the treatment scored 22. A new spinal tap showed normal CSF. Neurosyphilis should be part of the differential diagnosis of every patient showing cognitive deterioration and behaviour disturbances. During follow-up, MMS is an useful instrument to mesure cognitive decline and response to treatment.
    Type of Medium: Online Resource
    ISSN: 0004-282X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 2000
    detail.hit.zdb_id: 2053072-9
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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