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Artículos de revistas sobre el tema "Syphilis"

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Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 29 de julio de 2024

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1

Hidayatullah A, Hidayatullah y Zulmaeta Zulmaeta. "Early Congenital Syphilis: The Impact of Bad Antenatal Care". Andalas Obstetrics And Gynecology Journal 7, n.º 2 (30 de julio de 2023): 411–15. http://dx.doi.org/10.25077/aoj.7.2.411-415.2023.

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Syphilis is a systemic infectious disease caused by Troponema palidum. Syphilis is generally transmitted through sexual contact, but can also be transmitted vertically during pregnancy. Until now syphilis has become a world wide problem for pregnant women, WHO recommends syphilis tested by triple elimination (syphilis, hepatitis B, and HIV) during antenatal care for better pregnancy outcomes.21 year old female, diagnosed with primipara 32-33 weeks of gestational age active phase of labor, latent syphilis + intrauterine single live fetus with head presentation. The patient had never checked her pregnancy until the current gestational age, and only found out that she had syphilis accompanied by clinical symptoms. Birth of a baby with suspected congenital syphilis.Â

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2

Koshkin, S. V., T. V. Chermnykh, O. S. Kovrova y N. YU Ryabov. "A case of psoriasiform syphilid (from clinical practice)". Vestnik dermatologii i venerologii 92, n.º 3 (24 de junio de 2016): 90–96. http://dx.doi.org/10.25208/0042-4609-2016-92-3-90-96.

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The current article analyzes a clinical case of general psoriasis-form syphilid in a 28-year patient. Attention is paid to combination of exudative psoriasis and syphilis in in a sex partner. Problems of differential diagnosis for clinical evidence of secondary syphilis and psoriasis were analyzed.

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3

Cossa, H. A., S. Gloyd, R. G. Vaz, E. Folgosa, E. Simbine, M. Diniz y J. K. Kreiss. "Syphilis and HIV Infection among Displaced Pregnant Women in Rural Mozambique". International Journal of STD & AIDS 5, n.º 2 (marzo de 1994): 117–23. http://dx.doi.org/10.1177/095646249400500208.

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A cross-sectional study was conducted among displaced pregnant women in Mozambique to determine the prevalence and correlates of HIV infection and syphilis. Between September 1992 and February 1993, 1728 consecutive antenatal attendees of 14 rural clinics in Zambézia were interviewed, examined, and tested for HIV and syphilis antibodies. The seroprevalence of syphilis and HIV were 12.2% and 2.9%, respectively. Reported sexual abuse was frequent (8.4%) but sex for money was uncommon. A positive MHA-TP result was significantly associated with unmarried status, history of past STD, HIV infection, and current genital ulcers, vaginal discharge, or genital warts. Significant correlates of HIV seropositivity included anal intercourse, history of past STD, and syphilis. In summary, displaced pregnant women had a high prevalence of syphilis but a relatively low HIV seroprevalence suggesting recent introduction of HIV infection in this area or slow spread of the epidemic. A syphilils screening and treatment programme is warranted to prevent perinatal transmission and to reduce the incidence of chancres as a cofactor for HIV transmission.

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4

Sivayadevi, P. y Heber Anandan. "Retrospective analysis of demographic factors and changing pattern of clinical features of acquired syphilis at a tertiary care center in South India". International Journal of Research in Dermatology 4, n.º 4 (25 de octubre de 2018): 534. http://dx.doi.org/10.18203/issn.2455-4529.intjresdermatol20184456.

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<p class="abstract"><strong>Background:</strong> Syphilis presents with a wide range of mucocutaneous and systemic manifestations, which can mimic many other diseases. The pattern of acquired syphilis is changing in recent years because of widespread use of antibiotics and HIV infection which leads to under diagnosis. Aim was to study the demographic factors and changing pattern of clinical features of acquired syphilis.</p><p class="abstract"><strong>Methods:</strong> Retrospective analysis of all cases of sexually transmitted infections registered in the Department of Venereology, Thanjavur Medical College from January 2013 to December 2017 was done. The data regarding epidemiological, clinical and investigational details were recorded and analyzed for changing trends in incidence, pattern and clinical presentation of syphilis.<strong></strong></p><p class="abstract"><strong>Results:</strong> Of the total 14,672 cases attended theSTI clinic, 140 patients were diagnosed as having syphilis. There were 101 (79.4%) males and 39 (27.8%) females. Primary Syphilis was diagnosed in 18 (12.25%), Secondary syphilis in 38 (27.14%) and latent in 84 (60%) cases. Palmoplantar syphilide was the most common skin manifestation seen in 20 (52.63%) cases of secondary syphilis. 11 (7.85%) patients was human immunodeficiency virus (HIV) reactive.</p><p class="abstract"><strong>Conclusions:</strong> Our study indicates an increasing trend in the prevalence of syphilis cases in last 5 years with a rise in early symptomatic syphilis demanding steps to increase awareness among the general population.</p>

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5

Zavadsky, Valentin N. "PATHOGNOMIC MANIFESTATIONS OF SECONDARY SYPHILIS ON ORAL MUCOSA AND LIPS: CLINICAL CASES". Russian Journal of Skin and Venereal Diseases 21, n.º 2 (15 de abril de 2018): 130–38. http://dx.doi.org/10.18821/1560-9588-2018-21-2-130-138.

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Secondary syphilids on oral mucosa and lips are acute contagious; in addition, they are quite often the only clinical manifestation of the syphilis. Therefore the recognition of oral mucosal syphilids is an important, high-priority task. Purpose. To consider the peculiarities and clinical variants of oral mucosal syphilids, what may occur by usual examinations of patients. Material and methods. We observed 36 patients with secondary syphilis, who have syphilids on the oral mucosa or lips. It is presented 12 characteristic cases. The complex serodiagnostic tests for syphilis and HIV and clinical examination of all patients were maked. Results. The oral mucosal syphilids in hall cases (39-71%; p = 0.05), especially by recidive syphilis, were presented the MILIARY “point-papules” or “streak-papules” which grouped in the form of a “seed-pearls strings and rings”. The photographing is handy for their detection. Mucosal PLAQUES and lenticular papules are “delicate” (non-hard), opaline. They are marked but they accounted for little more of half of mucosal eruptions (50-81%; p = 0.05). Besides they were in ⅓ cases with miliary papules combined. Mucosal plaques are focal arranged or else they closely grouped (phenomenon “pseudo confluence”). Imaginary confluenсe of plaques, which are similar in size but various macerated, is particular specific (“mosaic lesion”). ERYTHEMA is out-lined, deep-red, in the form of “stamped” rounded sports (on the hard palate) or else as erythematous angina (on the molle palate) observed. Erythema were occurred in 13-41% of cases, often with papules were combined. PATHOGNOMIC indications of secondary syphilids are geometry regular form and grouping, rounded and out-lined contours, similarity in size. These peculiarities are attributable to the fact that eruptions are developed in places, where the circulating immune complexes (CIC) were fixated. CIC have bioelectric charge. Therefore, CIC arranged and fixed to a force isolines of natural electrostatic field in the tissue. These isolines have geometry regular form of arc or circle. The mechanism of CIC-fixation can be to describe by biophysical theory DLFO (Deryagin-Landau-Forway-Overbeck). The local conditions for CIC-fixation and for formation of infiltrate (papules) are created by lesions of small arterioles and local blood-stream disorders. Conclusion. Secondary syphilids on the oral mucosa are multiform. The use of photographing is handy for detection of miliary papules, which are often, but barely visible.

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6

Almeida, Filipa Tavares, Filomena Azevedo y Carmen Lisboa. "Syphilitic Balanitis of Follmann: Laboratory Pitfalls". Journal of the Portuguese Society of Dermatology and Venereology 78, n.º 3 (27 de septiembre de 2020): 265–68. http://dx.doi.org/10.29021/spdv.78.3.1199.

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We report a case of early syphilis, presenting as balanitis and papular syphilides in an HIV-infected patient, with a previous history of syphilis infection, which demonstrated a false negative VDRL testing due to a prozone phenomenon. This false negative response results from overwhelming antibody titers, which interfere with the proper formation of the antigen-antibody lattice network, necessary to visualize a positive flocculation test.

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7

Serdjukova, Е. А., V. V. Popov, O. A. Chernyavskaya y N. A. Morozova. "Secondary recurrent syphilis in a patient with HIV infection. Clinical case". HIV Infection and Immunosuppressive Disorders 16, n.º 1 (19 de abril de 2024): 86–91. http://dx.doi.org/10.22328/2077-9828-2024-16-1-86-91.

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Relevance. HIV infection is a chronic sexually transmitted infectious disease. Given the single route of transmission, quite often HIV-infected patients develop a syphilitic infection. At the same time, syphilis against the background of HIV infection has its own clinical characteristics. It is important for doctors of various specialties to know these features.Description of the case. A clinical case of secondary syphilis and early neurosyphilis in a 52-year-old patient with HIV infection is presented.Discussion. Patients with HIV infection are characterized by unusual clinical manifestations of syphilis in the form of its malignity, atypical, severe course with the development of various complications. In the article, the authors describe atypical manifestations of papular syphilide of the palms and soles. The effectiveness of specific treatment has been shown.Conclusions. Doctors’ knowledge of the clinical features of syphilis against the background of HIV infection will allow them to avoid diagnostic errors leading to late treatment and the development of complications.

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8

Syred, Jonathan, Chris Howroyd, Gillian Holdsworth, Kes Spelman y Paula Baraitser. "P121 Choose to test". Sexually Transmitted Infections 93, Suppl 1 (junio de 2017): A56.3—A57. http://dx.doi.org/10.1136/sextrans-2017-053232.165.

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IntroductionChoice is an increasingly important element of health care. We introduced choice of test into an online sexual health service.MethodsUsers were offered testing based on their risk profile (table 1) with an option to request additional tests. Routinely collected anonymised data were collected on choice of test.Abstract P121 Table 1Results from Choose to test<2424+BMEMSMGenital GC/CT*YesYesYesYesOral GC/CT*NoNoNoYesAnal GC/CT*NoNoNoYesSyphilisNoNoNoYesHIVNoNoYesYesResults2550 users ordered tests (30/10/16 – 19/12/16). 56% were <24, 10% were from black or ethnic minority (BME) groups and 17% were men who have sex with men (MSM). 1853 (72.6%) returned a test, 6.7% were positive for any STI. Of the non-BME/non-MSM users offered chlamydia/gonorrhoea testing, 66% chose to add HIV + syphillis testing. Of the BME/non-MSM users offered chlamydia/gonorrhoea + HIV testing, 71% chose to add syphilis testing. Of the MSM users offered chlamydia/gonorrhoea (genital, oral, anal) + HIV + syphilis testing, 85% chose this option. 6% chose to omit the HIV/syphilis test. User choice resulted in 611 fewer HIV tests, 596 fewer syphilis tests and 27 fewer chlamydia/gonorrhoea tests.DiscussionOnline service users actively exercise choice in STI test selection. The majority of users choose to test for chlamydia, gonorrhoea, HIV and syphilis regardless of what they are offered. User choice of test reduces the total number of tests offered online.

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9

Ratnaraj, Felicia, David Brooks, Mollie Walton, Arun Nagabandi y Mahmoud Abu Hazeem. "Forgotten but Not Gone! Syphilis Induced Tenosynovitis". Case Reports in Infectious Diseases 2016 (2016): 1–4. http://dx.doi.org/10.1155/2016/7420938.

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Objective. Tenosynovitis, inflammation of a tendon and its synovial sheath, is a rare manifestation of secondary syphilis and if diagnosed early is reversible.Background. A 52-year-old male with past medical history of untreated syphilis presented with gradual onset of swelling and pain of the right fourth metacarpophalangeal joint (MCP). He reported a history of painless penile lesions after having sexual intercourse with a new partner approximately five months ago which was treated with sulfamethoxazole/trimethoprim. An RPR done at that time came back positive with a high titer; however, patient was lost to follow-up. On examination, patient had an edematous, nonerythematous right fourth proximal interphalangeal (PIP) joint. Urgent irrigation, debridement, and exploration of the right hand into the tendon sheath were performed. With his history of syphillis, an RPR was done, which was reactive with a titer of 1 : 64. A confirmatory FTA-ABS test was completed, rendering a positive result. Based on his history of untreated syphilis, dormancy followed by clinical scenario of swelling of the right fourth finger, and a high RPR titer, he was diagnosed with secondary syphilis manifesting as tenosynovitis.

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10

Serdyukova, Elena A. y Svetlana N. Shchava. "Features of clinical manifestations of secondary syphilis in a HIV infected patient". Russian Journal of Skin and Venereal Diseases 27, n.º 1 (4 de marzo de 2024): 37–44. http://dx.doi.org/10.17816/dv623684.

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Syphilis and human immunodeficiency virus (HIV) infection are diseases of an infectious nature with a predominantly sexual route of infection. Despite the decrease in the incidence of syphilis in recent years in Russia, there is an increase in HIV infection. The combination of several infections in one patient leads to changes in clinical manifestations, which sometimes significantly complicates their diagnosis, leading to a late start of treatment. Syphilis against the background of HIV infection proceeds in stages, but usually it has a malignant, aggressive and severe course, often with the development of atypical forms and complications. The primary syphilis against the background of HIV infection is characterized by the appearance of ulcerative-necrotic character of the hard chancre, such severe complications as phagedenism and gangrenization, the frequent addition of a secondary infection, severe soreness of the hard chancre. Secondary syphilides in HIV-infected patients are characterized by the appearance of ulceration with the formation of necrotizing vasculitis, extraordinary infectiousness of the elements. The disease progresses rapidly and over a few months from the moment of infection, manifest neurosyphilis or tertiary syphilis may develop due to immunodeficiency. The authors describe the features of the manifestations of syphilis in its different periods against the background of HIV infection. A clinical case of a 35-year-old woman who was diagnosed with secondary syphilis and HIV infection is presented. The patient had numerous skin rashes, which were interpreted differently by doctors of different specialties for 2 months. The patient was diagnosed with pyoderma, "allergy", infectious exanthema, however, against the background of the treatment, there was a negative dynamics of the skin process. The authors have demonstrated the effectiveness of specific therapy: complete resolution of skin rashes.

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11

Jorge, Lívia Montelo Araújo, José Augusto da Costa Nery y Fred Bernardes Filho. "Tertiary syphilis: tubero-serpiginous and tubero-ulcerous syphilids". Brazilian Journal of Infectious Diseases 20, n.º 3 (mayo de 2016): 308–9. http://dx.doi.org/10.1016/j.bjid.2016.01.007.

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12

MÖLLER, MAGNUS. "Zur Kenntnis des pustulösen Syphilides (Syphilis maligna)." Nordiskt Medicinskt Arkiv 30, n.º 14 (24 de abril de 2009): 1–13. http://dx.doi.org/10.1111/j.0954-6820.1897.tb00239.x.

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13

Valikova, T. A., V. M. Alifirova, I. M. Fyodorova y N. Yu Paimursina. "The clinical manifestations of nervous system mesenchyme syphilis". Bulletin of Siberian Medicine 1, n.º 2 (30 de junio de 2002): 77–82. http://dx.doi.org/10.20538/1682-0363-2002-2-77-82.

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Nervous system syphilis — neurosyphilis (NS) belongs to rather rare diseases. According to the different authors data available it comes to about 1% of the nervous system organic disturbances and develops by 5—10% syphilous patients not having been treated in the acute stage of the pathological process. The syphilitic disturbance of the nervous system is a chronic progressive disease caused by the pale spirochaeta. The nervous system disturbance occurs basically in two ways: secondary one, because of brain shells, vessels, gummatous manifestations involving in the pathologic process; or primary one, when the causative agent affects directly the brain substance. In the first case syphilis is called rnesodermic or early one; in the second case — parenchymatous or late, primary one. In the article the analysis of two clinical cases of mesenchyme neurosyphilis is carried out: latent neurosyphilis and syphilitic meningomyelitis. Neurosyphilis classification is applied to clinical manifestatons of syphilitic arachnoiditis and vasculitis are described. The methods of specific and nonspecific therapy of mesenchyme syphilis are stated in detail.

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14

S, Deivam. "Withering Syphilis Management". Journal of Medical Science And clinical Research 04, n.º 12 (10 de diciembre de 2016): 14509–10. http://dx.doi.org/10.18535/jmscr/v4i12.35.

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15

Li, Yi y Bernard Gonik. "Is Congenital Syphilis Really Congenital Syphilis?" Infectious Diseases in Obstetrics and Gynecology 2006 (2006): 1–4. http://dx.doi.org/10.1155/idog/2006/81629.

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Detroit has recently been distinguished as having the highest congenital syphilis rate in the United States (250.3 cases per100 000live births in Detroit versus 10.3 in the US). However, depending on each health department's followup and CDC reporting, these data may not accurately reflect the true congenital syphilis rate. This study examines the reported cases over a three-year time period with focus on the criteria used for diagnosis. All local health department congenital syphilis CDC collection forms (form 73.126) were reviewed for the years in question. The reported congenital syphilis cases in the year 2002–2004 in Detroit were reviewed. No cases met confirmed case criteria and few probable cases were based on neonatal evaluations. The majority of “congenital syphilis” cases were established based on incomplete maternal data such as missing followup serologic titers in the absence of complete neonatal information. In conclusion, although the reported congenital syphilis rate in Detroit is alarmingly high, the true occurrence of congenital syphilis is likely to have been overstated. A health department reporting program that includes more diligent neonatal followup would allow for a more accurate representation of this public health concern.

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16

Musher, Daniel M. "Syphilis". Infectious Disease Clinics of North America 1, n.º 1 (marzo de 1987): 83–95. http://dx.doi.org/10.1016/s0891-5520(20)30098-2.

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17

Hyman, E. L. y H. M. Adam. "Syphilis". Pediatrics in Review 27, n.º 1 (1 de enero de 2006): 37–39. http://dx.doi.org/10.1542/pir.27-1-37.

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18

Butterfield, R. "Syphilis". Pediatrics in Review 35, n.º 5 (1 de mayo de 2014): 212–13. http://dx.doi.org/10.1542/pir.35-5-212.

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19

Darville, T. "Syphilis". Pediatrics in Review 20, n.º 5 (1 de mayo de 1999): 160–65. http://dx.doi.org/10.1542/pir.20-5-160.

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20

Leavesley, James. "Syphilis". Medical Journal of Australia 142, n.º 1 (enero de 1985): 55–57. http://dx.doi.org/10.5694/j.1326-5377.1985.tb113289.x.

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21

Potter, Yvonne. "Syphilis". Nursing Standard 23, n.º 2 (17 de septiembre de 2008): 59–60. http://dx.doi.org/10.7748/ns.23.2.59.s57.

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22

Melvin, Susan Y. "Syphilis". Primary Care: Clinics in Office Practice 17, n.º 1 (marzo de 1990): 47–57. http://dx.doi.org/10.1016/s0095-4543(21)00591-1.

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23

Butterfield, Rebecca. "Syphilis". Pediatrics In Review 35, n.º 5 (1 de mayo de 2014): 212–13. http://dx.doi.org/10.1542/pir.35.5.212.

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24

Darville, Toni. "Syphilis". Pediatrics In Review 20, n.º 5 (1 de mayo de 1999): 160–65. http://dx.doi.org/10.1542/pir.20.5.160.

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Hyman, Erica L. "Syphilis". Pediatrics In Review 27, n.º 1 (1 de enero de 2006): 37–39. http://dx.doi.org/10.1542/pir.27.1.37.

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Pariser, Harry. "Syphilis". Primary Care: Clinics in Office Practice 16, n.º 3 (septiembre de 1989): 603–19. http://dx.doi.org/10.1016/s0095-4543(21)01332-4.

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27

Siegel, David y A. Eugene Washington. "Syphilis". Postgraduate Medicine 81, n.º 1 (enero de 1987): 83–90. http://dx.doi.org/10.1080/00325481.1987.11699661.

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Wooldridge, Wilfred E. "Syphilis". Postgraduate Medicine 89, n.º 1 (enero de 1991): 193–202. http://dx.doi.org/10.1080/00325481.1991.11700797.

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Hu, Die, Ling Liu, Hao Tang y Dao-quan Peng. "Syphilis". Coronary Artery Disease 25, n.º 6 (septiembre de 2014): 540–41. http://dx.doi.org/10.1097/mca.0000000000000127.

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30

Robbins, Noah. "Syphilis". Infectious Diseases in Clinical Practice 27, n.º 4 (julio de 2019): 185. http://dx.doi.org/10.1097/ipc.0000000000000754.

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Goh, Beng. "Syphilis". Medicine 33, n.º 10 (octubre de 2005): 48–51. http://dx.doi.org/10.1383/medc.2005.33.10.48.

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Ballard, Ronald C. "Syphilis". Medicine 29, n.º 8 (agosto de 2001): 52–59. http://dx.doi.org/10.1383/medc.29.8.52.28396.

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MUSHER, DANIEL. "Syphilis". Pediatric Infectious Disease Journal 9, n.º 10 (octubre de 1990): 768. http://dx.doi.org/10.1097/00006454-199010000-00036.

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Mallory, Susan B. "Syphilis". Pediatric Dermatology 6, n.º 1 (marzo de 1989): 51–52. http://dx.doi.org/10.1111/j.1525-1470.1989.tb00267.x.

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Tillman, Jill. "Syphilis". Journal of Obstetric, Gynecologic & Neonatal Nursing 21, n.º 3 (mayo de 1992): 209–13. http://dx.doi.org/10.1111/j.1552-6909.1992.tb02257.x.

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Wasserheit, Judith N. "Syphilis". Sexually Transmitted Diseases 27, n.º 6 (julio de 2000): 311–12. http://dx.doi.org/10.1097/00007435-200007000-00002.

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Sukthankar, Ashish. "Syphilis". Medicine 38, n.º 5 (mayo de 2010): 263–66. http://dx.doi.org/10.1016/j.mpmed.2010.01.016.

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Sukthankar, Ashish. "Syphilis". Medicine 42, n.º 7 (julio de 2014): 394–98. http://dx.doi.org/10.1016/j.mpmed.2014.04.002.

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Young, Hugh. "SYPHILIS". Dermatologic Clinics 16, n.º 4 (octubre de 1998): 691–98. http://dx.doi.org/10.1016/s0733-8635(05)70034-6.

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Bonnetblanc, J. M. "Syphilis". Annales de Dermatologie et de Vénéréologie 131, n.º 5 (mayo de 2004): 513–15. http://dx.doi.org/10.1016/s0151-9638(04)93654-x.

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Larsen, Sandra A. "Syphilis". Clinics in Laboratory Medicine 9, n.º 3 (septiembre de 1989): 545–57. http://dx.doi.org/10.1016/s0272-2712(18)30618-8.

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Hollier, Lisa M. y Susan M. Cox. "Syphilis". Seminars in Perinatology 22, n.º 4 (agosto de 1998): 323–31. http://dx.doi.org/10.1016/s0146-0005(98)80021-9.

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Lewis, D. A. y H. Young. "Syphilis". Sexually Transmitted Infections 82, suppl_4 (1 de diciembre de 2006): iv13—iv15. http://dx.doi.org/10.1136/sti.2006.023085.

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Drusin, L. M. "Syphilis". Current Opinion in Infectious Diseases 2, n.º 1 (febrero de 1989): 11–15. http://dx.doi.org/10.1097/00001432-198902010-00004.

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Lukehart, Sheila A. "Syphilis". Current Opinion in Infectious Diseases 3, n.º 1 (febrero de 1990): 3–9. http://dx.doi.org/10.1097/00001432-199002000-00002.

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46

Janier, Michel y E´ric Caumes. "Syphilis". EMC - Dermatologie 1, n.º 1 (enero de 2006): 1–17. http://dx.doi.org/10.1016/s0246-0319(06)73799-2.

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47

Dupin, N. "Syphilis". La Revue de Médecine Interne 37, n.º 11 (noviembre de 2016): 735–42. http://dx.doi.org/10.1016/j.revmed.2016.05.010.

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Hook, Edward W. "Syphilis". Lancet 389, n.º 10078 (abril de 2017): 1550–57. http://dx.doi.org/10.1016/s0140-6736(16)32411-4.

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Barnett, Richard. "Syphilis". Lancet 391, n.º 10129 (abril de 2018): 1471. http://dx.doi.org/10.1016/s0140-6736(18)30833-x.

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Dupin, Nicolas y David Farhi. "Syphilis". La Presse Médicale 42, n.º 4 (abril de 2013): 446–53. http://dx.doi.org/10.1016/j.lpm.2012.09.024.

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