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         Neurosyphilis:     more books (49)
  1. The Wassermann sero-diagnosis of syphilis in its application to psychiatry by Felix Plaut, 1911
  2. Syphilis of the nervous system by Karl A Menninger, 1921
  3. Syphilis of the nervous system (A system of syphilis) by Frederick Walker Mott, 1914
  4. Syphilitic diseases of the spinal cord by R. T Williamson, 1899
  5. Syphilis of the nervous system by H. C Wood, 1889
  6. Syphilis of the central nervous system by Josephine Anne Girard, 1936
  7. Syphilis of the brain and spinal cord, showing the part which this agent plays in the production of paralysis, epilepsy, insanity, headache, neuralgia, ... Brain and diseases of the nervous system) by Thomas Stretch Dowse, 1881

61. Health Ency.: Disease: Neurosyphilis
neurosyphilis. Prevention. neurosyphilis can be prevented by the timelydiagnosis and treatment of primary syphilis and secondary syphilis.
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Ency. home Disease N Neurosyphilis Overview Symptoms Treatment Prevention Prevention Neurosyphilis can be prevented by the timely diagnosis and treatment of primary syphilis and secondary syphilis . Good follow-up of these early stages to absolutely demonstrate a cure is necessary to avoid neurosyphilis from developing following incomplete treatment (either by inadequate medication or non-compliance of the individual taking the medication). Ency. home Disease N Please read this Important notice Also Check Out
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62. Health Ency.: Disease: Neurosyphilis
neurosyphilis. eg, FTAAbs or MHATP). In neurosyphilis, it is importantto test for VDRL in the spinal fluid. Tests to evaluate the
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Ency. home Disease N Neurosyphilis Overview Symptoms Treatment Prevention Symptoms Note: There may be no symptoms (in the asymptomatic form) Signs and Tests Tests to detect syphilis include detection of antibodies in blood. These are non-treponemal tests (VDRL, RPR). These are not specific and are used as screening tests. If positive the diagnosis of syphilis is confirmed using treponemal tests (e.g., FTA-Abs or MHATP). In neurosyphilis, it is important to test for VDRL in the spinal fluid. Tests to evaluate the nervous system may include: Ency. home

63. About BrainLand Home
Discussion topic neurosyphilis. Go back to the list of all discussion topics;Click on the discussion topic name ( ) to start a new thread of messages ( ).
http://www.brainland.com/forums/treetest3new.cfm?cftreeitemkey=28

64. P010402a - CSF Evaluation Of Neurosyphilis
CSF Evaluation of neurosyphilis. 4/02/01 (Beer). Question What are the typicalCSF findings in neurosyphilis? 2 95141188. South African Medical Journal.
http://www.emory.edu/WHSCL/grady/amreport/litsrch00/p010402a.html
CSF Evaluation of Neurosyphilis 4/02/01 (Beer) RE: A young black male with HIV, headache, and positive serum RPR. Question: What are the typical CSF findings in neurosyphilis? South African Medical Journal. 84(10):682-4, 1994 Oct. The usefulness of cerebrospinal fluid tests for neurosyphilis. British Journal of Venereal Diseases. 57(4):232-7, 1981 Aug. Diagnosis of neurosyphilis by examination of the cerebrospinal fluid. Unique Identifier: 95141188 Authors: Russouw HG. Roberts MC. Emsley RA. Joubert JJ. Institution: Department of Psychiatry, University of Stellenbosch, Tygerberg, W. Cape. Title: The usefulness of cerebrospinal fluid tests for neurosyphilis. Source: South African Medical Journal. 84(10):682-4, 1994 Oct. Unique Identifier: 82001369 Authors: Luger A. Schmidt BL. Steyrer K. Schonwald E. Title: Diagnosis of neurosyphilis by examination of the cerebrospinal fluid. Source: British Journal of Venereal Diseases. 57(4):232-7, 1981 Aug. Morning Report Emory University School of Medicine 2000 Edition Participating Faculty: Daniel Stephens MD / Donald Brady MD dbrady@emory.edu

65. P990819a - Neurosyphilis (Tertiary)
neurosyphilis (Tertiary). 8/19/99 (Stephens). Question What are the clinicalcharacteristics of tertiary neurosyphilis? 1 . Unique Identifier 99212045.
http://www.emory.edu/WHSCL/grady/amreport/litsrch99/p990819a.html
Neurosyphilis (Tertiary) (Stephens) Question: What are the clinical characteristics of tertiary neurosyphilis? Unique Identifier: 99212045 Authors: Singh AE. Romanowski B. Institution: Alberta Health STD Services, University of Alberta, Edmonton, Alberta, Canada. Title: Syphilis: review with emphasis on clinical, epidemiologic, and some biologic features. [Review] [370 refs] Source: Clinical Microbiology Reviews. 12(2):187-209, 1999 Apr. Abstract: Unique Identifier: 99060827 Authors: Bharwani IL. Hershey CO. Institution: State University of New York at Buffalo, USA. Title: The elderly psychiatric patient with positive syphilis serology:the problem of neurosyphilis. [Review] [27 refs] Source: International Journal of Psychiatry in Medicine. 28(3):333-9, 1998. Abstract: Unique Identifier: 95197849 Authors: Scheck DN. Hook EW 3rd. Institution: University of Alabama School of Medicine, Birmingham. Title: Neurosyphilis. [Review] [171 refs] Source: Infectious Disease Clinics of North America. 8(4):769-95, 1994 Dec. Abstract: Central nervous system invasion by Treponema pallidum, the causative agent of syphilis, occurs in many, if not most, patients with syphilis. Laboratory findings from untreated asymptomatic syphilis patients with abnormalities of cerebrospinal fluid are termed asymptomatic neurosyphilis and represent a group that has an increased risk for developing clinical neurosyphilis syndromes. Clinical neurosyphilis syndromes, which occur in a minority of patients, may become apparent at any time in the natural history of untreated disease and often causeserious morbidity for individuals who develop them. Because there is no single sensitive and highly specific test for neurosyphilis diagnosis, clinicians must approach this important syndrome using a combination of clinical and laboratory data and a firm understanding of the disease. [References: 171]

66. Forum : Neurologie
Translate this page neurosyphilis, par MOHI YOUSSEF, le 02 Sep 98 à 192944 Reneurosyphilis, parbahji mostafa service de neurologie HMI.MV rabat MAROC, le 10 Sep 99 à 0222
http://www.med.univ-rennes1.fr/cgi-bin/uv/forum.pl?neuro

67. Neurosyphilis
neurosyphilis. Definition neurosyphilis occurs in 15 to 20% of all late or tertiarysyphilis infections and is a progressive, lifethreatening complication.
http://www.northarundel.com/ency/article/000703.htm
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Neurosyphilis
Overview Symptoms Treatment Prevention Definition: Neurosyphilis is a slowly progressive and destructive infection of the brain or spinal cord that occurs in untreated syphilis many years after the primary infection.
Causes, incidence, and risk factors: Neurosyphilis occurs in 15 to 20% of all late or tertiary syphilis infections and is a progressive, life-threatening complication. There are 4 different forms of neurosyphilis: asymptomatic , meningovascular, tabes dorsalis , and general paresis
Asymptomatic neurosyphilis precedes symptomatic syphilis and is present in 15% of those with latent syphilis. In this case, abnormalities may be present in the cerebrospinal fluid, but no symptoms are present.
In meningovascular neurosyphilis, cranial nerve palsies and pupillary abnormalities may be present with a wide variety of symptoms. This may also cause damage to blood vessels resulting in stroke.
In tabes dorsalis, progressive degeneration of the spinal cord occurs causing an inability to walk.
In general paresis

68. Latebreaker Abstracts - 2002 National STD Prevention Conference
Latebreaker Abstracts. Back to Table of Contents. Risk Factors for neurosyphilis. Itis difficult to predict which patients will progress to neurosyphilis.
http://www.cdc.gov/nchstp/dstd/2002ConfAbstracts/2002ConfAbLatebreaker.htm
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What's New Index Search ... Contact Us 2002 National STD Prevention Conference - Abstracts Latebreaker Abstracts Back to Table of Contents Risk Factors for Neurosyphilis CM Marra , CL Maxwell , SL Smith , SA Lukehart , AM Rompalo , M Eaton , BP Stoner , DE Barker , JJ Corbett , M Augenbraun , M Zajackowski , C Raines , J Nerad , R Kee , SH Barnett 1Departments of Neurology and 2Medicine (Infectious Diseases), University of Washington School of Medicine, Seattle, WA; 3Department of Medicine, Johns Hopkins University, Baltimore, MD; 4Department of Medicine, Emory University, Atlanta, GA; 5Department of Medicine, Washington University, St. Louis, MO; 6Rush Medical College, Chicago, IL; 7Department of Neurology, University of Mississippi, Jackson, MS; 8Department of Medicine, SUNY-Downstate, Brooklyn, NY; 9Chicago Department of Health, Chicago, IL Background: Treponema pallidum invades the central nervous system (CNS) early in infection. About 75% of patients clear CNS treponemes; those who do not are at risk for neurosyphils. It is difficult to predict which patients will progress to neurosyphilis.

69. Case Definitions Print Page
neurosyphilis. Clinical description. Syphilis, late, with clinical manifestationsother than neurosyphilis (late benign syphilis and cardiovascular syphilis).
http://www.cdc.gov/epo/dphsi/print/syphilis_current.htm
Syphilis (Treponema pallidum)
1996 Case Definition
Syphilis is a complex sexually transmitted disease that has a highly variable clinical course. Classification by a clinician with expertise in syphilis may take precedence over the following case definitions developed for surveillance purposes.
Syphilis, primary
Clinical description
A stage of infection with Treponema pallidum characterized by one or more chancres (ulcers); chancres might differ considerably in clinical appearance.
Laboratory criteria for diagnosis
  • Demonstration of T. pallidum in clinical specimens by darkfield microscopy, direct fluorescent antibody (DFA-TP), or equivalent methods.
Case classification
Probable : a clinically compatible case with one or more ulcers (chancres) consistent with primary syphilis and a reactive serologic test (nontreponemal: Venereal Disease Research Laboratory [VDRL] or rapid plasma reagin [RPR]; treponemal: fluorescent treponemal antibody absorbed [FTA-ABS] or microhemagglutination assay for antibody to T. pallidum

70. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE
Stimulation. neurosyphilis. See DORSALIS; neurosyphilis Search PUBMED forarticles on neurosyphilis All Review Therapy Diagnosis. NEUROTHERAPY. See
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Patienten en leken die raadgevingen/adviezen/informatie zoeken via deze verzameling links wordt dringend geadviseerd de verzamelde informatie te bespreken met de (behandelend) arts/specialist/hulpverlener.
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  • 71. NEUROSYPHILIS (in MARION)
    neurosyphilis. neurosyphilis. (LC) (about) (6 titles) Search alsounder Locomotor ataxia. neurosyphilis. (MeSH) (about) (13 titles
    http://atlas.hslc.org:8007/MARION?S=NEUROSYPHILIS

    72. ICP Monitors
    neurosyphilis. Benign tertiary stage. neurosyphilis. Cardiovascular syphilis.Classification of neurosyphilis. A) Asymptomatic. B) Meningeal and Vascular.
    http://www.ucch.org/sections/neurosurg/NeuroReview/12-CNS Infections/Neurosyphil
    Neurosyphilis Treponema pallidum Classification of Syphilis Early Primary Stage . Chancre and regional lympadenopathy. Secondary Stage . Immediately follows primary stage and consists of various dermatologic lesions. Latent . Asymptomatic and may persist indefinitely. Late or Tertiary Stage . Benign tertiary stage. Neurosyphilis. Cardiovascular syphilis. Classification of Neurosyphilis A) Asymptomatic B) Meningeal and Vascular Cerebral meningeal. Diffuse and focal forms. Cerebrovascular Spinal meningeal and vascular C) Parenchymatous Tabetic Paretic Optic atrophy Asymptomatic Neurosyphilis Meningeal and Vascular Cerebral Meningeal i) Increased ICP from blockage of CSF pathways. ii) Damage to cranial nerves. iii) Focal deficits from thrombosis of small vessels. gumma is a syphlitic granuloma that may occur in association with the dura and is classified as a localized form of meningeal syphilis. Symptoms mimic that of a brain tumor. Cerebrovascular Spinal Meningeal Parenchymatous Paretic dementia paralytica or general paresis of the insame . Spirochetes cause a chronic meningoencephalitis. The leptomeninges are thickened and attached to the cortex. The walls of the ventricles are covered with granulations called granular ependymitis Tabetic locomotot ataxia . Present with lancinating pains, ataxia, and loss of bowel, bladder and sexual function.

    73. Eurosurveillance Weekly - Volume 6 - Issue 11 (14/03/2002)
    An evaluation of contact tracing in tuberculosis neurosyphilisGerman recommendations for selective screening.
    http://www.eurosurveillance.org/ew/2002/020314.asp

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    Eurosurveillance Weekly archives 2002 > Volume 6 / Issue 11 page précédente
    Surveillance Report volume issue date 14 mars 2002
  • An evaluation of contact tracing in tuberculosis
  • Neurosyphilis: German recommendations for selective screening An evaluation of contact tracing in tuberculosis Contact tracing is an important part of tuberculosis (TB) prevention and control in low incidence countries (1,2). It aims primarily to identify individuals with latent or active TB who have been in contact with patients with infectious TB so that appropriate preventive or curative treatment can be given. The importance of contact tracing has been reinforced in recent studies using molecular typing methods which have shown that up to a third of patients in some industrialised countries have evidence of recent transmission of TB rather than reactivation of old tuberculous infection (3-5). A recent paper (6) presents an evaluation of contact tracing as practised in the United States. The study, which was carried out in 1996 at five study sites, assessed 349 patients (aged 15 years and over) with pulmonary TB and their 3824 contacts. An average of 1.9 infected contacts were found for each case of TB (2.6 per smear positive patient and 1.2 per smear negative patient), and positive tuberculin skin tests or active disease in 18% of contacts. In an earlier American study (7), up to 36% of contacts were found to have evidence of infection or disease. The paper recommends that a standard approach to TB contact investigation has the potential to improve outcomes and that better follow up of contacts is an important public health priority to improve TB prevention and control.
  • 74. Syphilis: A Treatment Lesson From AIDSmeds.com
    Syphilis neurosyphilis. What is it? Syphilis is a disease causedby the organism Treponema pallidum. It is a sexually transmitted
    http://www.aidsmeds.com/OIs/Syphilis1.htm
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    What is it? Syphilis is a disease caused by the organism Treponema pallidum . It is a sexually transmitted disease (STD), meaning that it is spread through sexual activity with someone infected with the bacterium. The infection usually causes disease over a course of several years. If it is not treated early or correctly, it can lead to serious problems, such as heart problems, mental disorders and neurologic problems (neurosyphilis), blindness, dementia, and death. Syphilis is passed from person to person through direct contact with a syphilis sore or lesion. Sores develop early in the course of syphilis, occurring mainly on the external genitals, vagina, anus, or in the rectum. Sores also can occur on the lips and in the mouth. It's important to note that these sores are not painful, so a person might not notice them. Transmission of the organism occurs during vaginal, anal, or oral sex. Pregnant women with the disease can pass it to the babies they are carrying. Rash-like lesions can appear on any part of the body after the sores heal, and are also infectious. Syphilis cannot be spread by toilet seats, door knobs, swimming pools, hot tubs, bath tubs, shared clothing, or eating utensils.

    75. 100. Jahrestagung Der DOG, 26.-29.9.2002: Optikusmanifestation Einer Neurosyphil
    Translate this page Optikusmanifestation einer neurosyphilis. Hasche H., Grehn F., Bayerische Julius-Maximilians-UniversitätWürzburg, Universitäts-Augenklinik (Würzburg).
    http://www.dog.org/2002/abstracts/677_d.html

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    Optikusmanifestation einer Neurosyphilis Hasche H., Grehn F.,
    Bayerische Julius-Maximilians-Universität Würzburg, Universitäts-Augenklinik (Würzburg)
    Hintergrund: Die in den letzten Monaten deutlich steigende Inzidenz von Syphilis ist nicht allein auf eine verbesserte Erfassung nach Umstellung des Meldesystems zurückzuführen (Meldepflicht des diagnostizierenden Labors, Infektionsschutzgesetz 2001). Vor allem bei Risikogruppen in großstädtischen Regionen zeigt sich ein signifikanter Anstieg der Fallzahlen. Eine frühe Diagnose und Therapie haben vor allem wegen des erhöhten HIV-Infektionsrisikos besondere Relevanz.
    Kasuistik:
    Schlussfolgerungen: Die Augenbeteiligung bei tertiärer symptomatischer Lues zeigt unterschiedliche klinische Manifestationen. Bei der Abklärung unklarer intraokularer Entzündungen sollte bei aktuell steigender Inzidenz der Erkrankung die Luesserologie weiterhin zur Standarddiagnostik gehören. Zurück/Back Last updated: Webdesign: SPALLEK.COM

    76. ¿À·ÐÇßÆÇ Neurosyphilis
    The summary for this Japanese page contains characters that cannot be correctly displayed in this language/character set.
    http://www31.tok2.com/home/akimichi/aki/medical/neurology/node23.html
    Next: Ǿ±ê encephalitis Up: Previous: ¿ñËì±ê meningitis
    Subsections

    ¿À·ÐÇßÆÇ neurosyphilis
    • ÀÔ¿ñáô tabes dorsalis ÀÔ¿ñ¸åº¬¤È¸åº÷¤ÎÊÑÀ­¤¬¸¶°ø¤È¤Ê¤¤Æ¡¢ÇÓÇ¢¾ã³²¡¦Rombergħ¸õ¡¦RobertsonÆ·¹¦¡¦²¼»èç§È¿¼Í¾¼º¤Ê¤É¤¬À¸¤¸¤ë¡£ ÇßÆÇ´¶À÷¤«¤é½½¿ôǯ¸å¤Ëȯ¾É¤¹¤ë¡£ ¿Ê¹ÔËãáã progressive paralysis ¥´¥à¼ð gumma
    • Argyll RobertsonÆ·¹¦ ξ¦À­È¿¼ÍÀ­¤ÎÆúºÌ³çÌó¶Ú¤ÎËãáã¤Ç¤¢¤ê¡¢Âи÷È¿¼Í¤Ï¾¼º¤¹¤ë¤¬íÕíÔÈ¿¼Í¤ÏÀµ¾ï¤ÇíÕíԤˤè¤ê¤¹¤ß¤ä¤«¤Ë½ÌÆ·¤¹¤ë¡£ »ë³¸Á°Ì¤é Edinger-Westphal³Ë´Ö¤Î¾ã³²¤Ç¤¢¤ê¡¢æ¿õÀ­¿À·ÐÇßÆǤËÆħŪ¤À¤¬¡¢¦¿ñ¼À´µ¤ä¾¾²ÌÂμðáç¤Ç¤â¸« ¤é¤ì¤ë¡£
    ÀÔ¿ñáô tabes dorsalis
    • ÀÔ¿ñ¸åº¬¤È¸åº÷¤ÎÊÑÀ­¤¬¸¶°ø¤È¤Ê¤¤Æ¡¢ÇÓÇ¢¾ã³²¡¦Rombergħ¸õ¡¦RobertsonÆ·¹¦¡¦²¼»èç§È¿¼Í¾¼º¤Ê¤É¤¬À¸¤¸¤ë¡£ ÇßÆÇ´¶À÷¤«¤é½½¿ôǯ¸å¤Ëȯ¾É¤¹¤ë¡£

    Akimichi Tatsukawa

    77. Volume 55 January - December 1932
    Certain pathological aspects of neurosyphilis. RO . Stern. Pages145 180. Part of the OUP Brain WWW service. General Information.
    http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_55/Issue_02/550145.sgm.
    Volume 55: January - December 1932
    Issue 2: June 1932
    Abstract
  • Certain pathological aspects of neurosyphilis
  • RO Stern Pages: Part of the OUP Brain WWW service
    General Information
    Click here to register with OUP. This page is maintained by OUP admin Last updated 13 May 97 Part of the OUP Journals World Wide Web service Oxford University Press, 1997

    78. Diagnostic Medical Testing In Psychiatric Disorders - Dementia - Syphilis Recomm
    Recommended Tests for neurosyphilis Qualitative Rapid Plasma Reagin (RPR) CPT86592Source Blood, serum; minimum 5 mL blood (1 mL serum) Use red-top tube
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    Recommended Tests for Neurosyphilis
    Qualitative Rapid Plasma Reagin (RPR) [CPT-86592]
    Source : Blood, serum; minimum 5 mL blood (1 mL serum): Use red-top tube or gel-barrier tube. A lavender-top (EDTA plasma) tube or blue-top (sodium citrate plasma) tube may be used when serum cannot be obtained.
    Handling : Specimen should be transported to the laboratory with minimum delay. If delay is expected, refrigerate the specimen.
    Special handling : Inappropriate specimen container, insufficient volume, lipemic, hemolyzed or chylous specimens are rejected.
    Microhemagglutination for T. pallidum specific antibodies [CPT-86781]
    Source : Blood, serum; minimum 5 mL blood (1 mL serum): Use red-top tube or gel-barrier tube. A green-top (heparin plasma) tube or lavender-top (EDTA plasma) tube or blue-top (sodium citrate plasma) tube may be used when serum cannot be obtained.
    Handling : Specimen should be transported to the laboratory with minimum delay. If delay is expected, refrigerate the specimen.

    79. Diagnostic Medical Testing In Psychiatric Disorders - Dementia - Diagnostic Crit
    neurosyphilis Diagnostic Criteria. Symptoms of neurosyphilis are usually dividedAsymptomatic neurosyphilis Most common presentation of neurosyphilis;
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    DSM-IV and ICD9 Coding Neurosyphilis Diagnostic Criteria
    The clinical manifestations of syphilis can be broadly classified [ ref
    • Primary syphilis
      • Presence of a chancre, a painless ulcerated lesion with a clean base, at the site of inoculation is a pathognomonic sign of primary syphilis.
      • Size of chancre ranges from 0.3 to 3.0 cm.
      • Multiple lesions may be present.
      • Incubation period varies from 3 to 90 days (mean, 3 weeks).
      • Regional lymphadenopathy is present in up to 80% of patients.
    • Secondary syphilis
      • Symptoms are due to the active multiplication and dissemination of spirochetes.
      • Onset of symptoms usually begins 2-8 weeks after the appearance of primary chancre.
      • Primary chancre still may be present in about one-third of patients.
      • Systemic manifestations include low-grade fever, malaise, pharyngitis, laryngitis, anorexia, weight loss, arthralgias, and generalized painless lymphadenopathy. Enlargement of epitrochlear lymph nodes should suggest diagnosis of the disease.
      • Skin manifestations are the hallmark of this stage of the disease.

    80. Infectious Disease - Syphilis
    Without cardiac or CNS involvement. neurosyphilis. neurosyphilis, tabesdorsalis, locomotor ataxia. Copyright 9/98 General Cologne Life RE.
    http://lifehealth.facworld.com/WTS/lifeonline/online/Infect_50/INF_Syphilis.htm
    Venereal Disorders Syphilis Congenital Syphilis Laboratory Tests Positive Wassermann, VDRL, FTA-ABS or TPI Primary, Secondary, Tertiary, or Latent Syphilis Without cardiac or CNS involvement Neurosyphilis Neurosyphilis, tabes dorsalis, locomotor ataxia

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