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1.
J Emerg Med ; 48(3): e59-62, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25511465

RESUMO

BACKGROUND: Fitz-Hugh-Curtis syndrome is a rare extra-pelvic complication of genital infection involving the perihepatic capsule. Most cases have been described in women in association with pelvic inflammatory disease; in rare cases it has been reported in men. Because the main symptom is acute abdominal pain, and laboratory and imaging findings are frequently nonspecific, the differential diagnosis, considering other gastrointestinal or renal diseases, can be difficult in the early stage of the syndrome, leading to frequent misdiagnosis and mismanagement. CASE REPORT: We report a case of Fitz-Hugh-Curtis syndrome in a 26-year-old man who first presented to the emergency department with acute abdominal pain, vomiting, and fever. Diagnosis was possible on the basis of clinical signs of orchiepididymitis, abnormal ultrasound findings, and specialist consultation with the Sexually Transmitted Infection Clinic. An acute gonoccocal infection was revealed, which was complicated by a collection of free perihepatic fluid and a subcapsular hypoechoic focal lesion. Prompt antibiotic therapy was established, with complete resolution of the symptoms within a few days. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: Awareness of the clinical presentation, imaging, and laboratory findings during the acute phase of Fitz-Hugh-Curtis syndrome could help emergency physicians to make an early diagnosis and to correctly manage such patients. Improved diagnostic skills could prevent chronic complications that are especially a risk in the case of delayed or minor genitourinary symptoms.


Assuntos
Infecções por Chlamydia/diagnóstico , Infecções por Chlamydia/microbiologia , Gonorreia/complicações , Hepatite/diagnóstico , Hepatite/microbiologia , Doença Inflamatória Pélvica/diagnóstico , Doença Inflamatória Pélvica/microbiologia , Peritonite/diagnóstico , Peritonite/microbiologia , Dor Abdominal/microbiologia , Doença Aguda , Adulto , Diagnóstico Diferencial , Febre/microbiologia , Humanos , Masculino , Vômito/microbiologia
2.
Dermatol Ther ; 26(2): 173-5, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23551375

RESUMO

Pruritic papular eruption (PPE) is a skin disease characterized by the eruption of itching papules on the extremities, face, and trunk; it is quite frequent in HIV-positive patients especially during the advanced immunosuppressive stage. PPE usually improves or heals when antiretroviral therapy restores the immune system function, but in some cases, it can take several months, and a symptomatic treatment for PPE is required. Systemic antihistamines, topical steroids, topical tacrolimus, itraconazole, pentoxyphilline, and ultraviolet B phototherapy have been proposed in cases of persisting PPE, but an elective treatment has not yet been found. We describe the case of a black patient affected by PPE, nonimproving with antiretroviral treatment, and resistant to topical steroids and oral antihistamines; a satisfactory and speedy result was achieved with narrow-band ultraviolet B phototherapy.


Assuntos
Infecções por HIV/complicações , Prurido/radioterapia , Dermatopatias Vesiculobolhosas/radioterapia , Terapia Ultravioleta/métodos , Adulto , Feminino , Humanos , Prurido/etiologia , Dermatopatias Vesiculobolhosas/etiologia , Dermatopatias Vesiculobolhosas/patologia , Resultado do Tratamento
3.
Dermatol Ther ; 25(1): 92-4, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22591503

RESUMO

Inflammatory linear verrucous epidermal nevus (ILVEN) is normally associated with the failure of topical and systemic treatments and with recurrences on interruption of therapy. Many physical approaches have been used, but they generally resulted in varying rates of recurrence and unacceptable scarring. We reported a case of ILVEN treated with a single session CO(2) laser treatment. In our experience, CO(2) laser was quick, easy, effective, and safe; we therefore believe that this approach should be considered as a first-line surgical option in the treatment of genital ILVEN, particularly in cases of mucosal involvement.


Assuntos
Lasers de Gás/uso terapêutico , Nevo Sebáceo de Jadassohn/cirurgia , Doenças da Vulva/cirurgia , Adulto , Feminino , Seguimentos , Humanos , Lasers de Gás/efeitos adversos , Nevo Sebáceo de Jadassohn/patologia , Resultado do Tratamento , Doenças da Vulva/patologia
4.
J Low Genit Tract Dis ; 15(4): 287-91, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21959572

RESUMO

OBJECTIVE: : The purpose of our study was to evaluate whether briefs made of Dermasilk fabric could be an adjuvant tool in the management of vulvar lichen sclerosus (LS). MATERIALS AND METHODS: : A controlled, randomized, double-blind study versus placebo was conducted, comparing Dermasilk versus standard cotton briefs in patients affected by LS during treatment with clobetasol propionate 0.05% ointment and vitamin E moisturizer. For each patient, an evaluation of objective genital signs and subjective symptoms typical of LS was recorded before the start of treatment, after 1 month, and after 6 months of the study. Statistical analysis was performed with SPSS 17.0 for Windows. RESULTS: : Forty-two women affected by LS were recruited and divided into those wearing Dermasilk or cotton briefs. Patients wearing Dermasilk briefs showed a better improvement in the clinical symptoms of burning sensation, skin irritation, and pain (Fisher test, p < .0001) compared with the cotton placebo group. The improvement in itching was also faster in the Dermasilk group (Fisher exact test, p < .05). Erythema also showed a better improvement in the Dermasilk group (Fisher test, p < 0.05). CONCLUSIONS: : Dermasilk fabric seems to be a useful adjunct to topical treatment in producing a better and more rapid control of symptoms in patients with LS.


Assuntos
Vestuário , Têxteis , Líquen Escleroso Vulvar/terapia , Adulto , Idoso , Anti-Inflamatórios/administração & dosagem , Clobetasol/administração & dosagem , Fibra de Algodão , Método Duplo-Cego , Feminino , Humanos , Pessoa de Meia-Idade , Placebos/administração & dosagem , Resultado do Tratamento , Vitamina E/administração & dosagem
5.
J Am Acad Dermatol ; 55(3): 438-41, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16908349

RESUMO

BACKGROUND: The prognosis of alopecia areata (AA) is difficult to predict. Few studies report long-term follow-up of AA patients. OBJECTIVE: The purpose of this study is to better assess the long-term evolution of AA and the possible relationship between disease severity and treatment response with long-term prognosis. METHODS: One hundred ninety-one patients with AA who presented with a new diagnosis of AA between 1983 and 1990 were subsequently contacted by phone. Patients were queried regarding current disease status, treatments, and disease course. RESULTS: Severity of AA at first consultation ranged from mild (128 patients) to severe (63 patients). Fifty-five of 191 patients were affected by concomitant autoimmune or related inflammatory disease. Sixty-six of 191 patients were presently disease free (follow-up duration, 15-22 years; mean 17.74 years). These include 41 of 60 patients with S1 disease (68.3%), 22 of 68 patients with S2 disease (32.3%), 1 of 11 patients with S3 disease (9%), 1 of 14 patients with S4 disease (7.1%), and 1 of 11 patients with alopecia totalis (AT) (9.1%). Sixty-nine of 191 patients (36-1%) were presently affected by AT or alopecia universalis. There was a statistically significant tendency of severe patterns of AA to worsen over time. In children, 18 of 39 (13 with < or =S2 disease and 5 with > or =S3 disease) with AA had developed AT or alopecia universalis at long-term follow-up. In children, however, this trend was not statistically significant. Patients with severe AA who responded to topical immunotherapy seem to have a better prognosis than nonresponders. LIMITATIONS: Follow-up was only performed by phone. CONCLUSIONS: Severity of AA at time of first consultation is an important prognostic factor. Response to therapy (topical immunotherapy) may be associated with better prognosis. In children, the prognosis is worse; our study found that AA worsens over time.


Assuntos
Alopecia em Áreas/tratamento farmacológico , Alopecia em Áreas/patologia , Administração Tópica , Adolescente , Adulto , Idoso , Alopecia em Áreas/complicações , Criança , Pré-Escolar , Progressão da Doença , Feminino , Ficusina/uso terapêutico , Seguimentos , Humanos , Imunoterapia , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Fármacos Fotossensibilizantes/uso terapêutico , Prognóstico , Estudos Retrospectivos , Índice de Gravidade de Doença , Esteroides/uso terapêutico , Terapia Ultravioleta
7.
BMC Res Notes ; 7: 225, 2014 Apr 09.
Artigo em Inglês | MEDLINE | ID: mdl-24716676

RESUMO

BACKGROUND: We evaluated LGV prevalence and predictors in a high risk population attending a STI Outpatients Clinic in the North of Italy. METHODS: A total of 108 patients (99 MSM and 9 women), with a history of unsafe anal sexual intercourses, were enrolled. Anorectal swabs and urine samples were tested for Chlamydia trachomatis (CT) DNA detection by Versant CT/GC DNA 1.0 Assay (Siemens Healthcare Diagnostics Terrytown, USA). RFLP analysis was used for CT molecular typing. RESULTS: L2 CT genotype was identified in 13/108 (12%) rectal swabs. All LGV cases were from MSM, declaring high-risk sexual behaviour and complaining anorectal symptoms. Patients first attending the STI Outpatient Clinic received a significant earlier LGV diagnosis than those first seeking care from general practitioners or gastroenterologists (P = 0.0046). LGV prevalence and characteristics found in our population are in agreement with international reports. Statistical analysis showed that LGV positive patients were older (P = 0.0008) and presented more STIs (P = 0.0023) than LGV negative ones, in particular due to syphilis (P < 0.001), HIV (P < 0.001) and HBV (P = 0.001).Multivariate logistic regression analysis revealed that HIV and syphilis infections are strong risk factors for LGV presence (respectively, P = 0.001 and P = 0.010). CONCLUSIONS: Even if our results do not provide sufficient evidence to recommend routine screening of anorectal swabs in high-risk population, they strongly suggest to perform CT NAAT tests and genotyping on rectal specimens in presence of ulcerative proctitis in HIV and/or syphilis-positive MSM. In this context, CT DNA detection by Versant CT/GC DNA 1.0 Assay, followed by RFLP analysis for molecular typing demonstrated to be an excellent diagnostic algorithm for LGV identification.


Assuntos
Canal Anal/microbiologia , Infecções por HIV/epidemiologia , Hepatite B/epidemiologia , Linfogranuloma Venéreo/epidemiologia , Assunção de Riscos , Sífilis/epidemiologia , Adolescente , Adulto , Instituições de Assistência Ambulatorial , Canal Anal/patologia , Canal Anal/virologia , Chlamydia trachomatis/genética , Chlamydia trachomatis/isolamento & purificação , Coinfecção , Feminino , Genótipo , Infecções por HIV/diagnóstico , Infecções por HIV/virologia , Hepatite B/diagnóstico , Hepatite B/virologia , Homossexualidade Masculina , Humanos , Itália/epidemiologia , Linfogranuloma Venéreo/diagnóstico , Linfogranuloma Venéreo/microbiologia , Masculino , Pessoa de Meia-Idade , Tipagem Molecular , Pacientes Ambulatoriais , Prevalência , Proctite/diagnóstico , Proctite/patologia , Fatores de Risco , Sífilis/diagnóstico , Sífilis/microbiologia , Sexo sem Proteção
10.
Salud(i)ciencia (Impresa) ; 18(2): 133-137, mar. 2011. ilus
Artigo em Espanhol | LILACS | ID: lil-610111

RESUMO

La sífilis es una enfermedad venérea causada por Treponema pallidum; su incidencia se incrementó durante las últimas dos décadas. Cuando una embarazada infectada no es tratada correctamente, puede transmitir la enfermedad al feto por vía transplacentaria. Al menos 2 de cada 3 de los neonatos de madres con sífilis durante el embarazo presentan una de estas alteraciones: hidropesía fetal, muerte intrauterina, parto prematuro, bajo peso al nacer o sífilis congénita. Los neonatos pueden encontrarse asintomáticos al momento del nacimiento y presentar las manifestaciones clínicas después de algunas semanas. La sífilis congénita se define como temprana si los síntomas aparecen entre el nacimiento y los primeros 2 años de vida, o tardía si las manifestaciones surgen a partir de los 2 años. Los signos clínicos más frecuentes son las alteraciones del sistema reticuloendotelial, el compromiso cutáneo, la afección esquelética y las anomalías dentales y oculares. El diagnóstico de sífilis congénita no es sencillo y se fundamenta en la evaluación clínica, la ecografía, las pruebas de laboratorio, la comparación entre las serologías de la madre y del niño, la radiología ósea y la evaluación del líquido cefalorraquídeo. El tratamiento consiste en la administración de penicilina. La sífilis congénita puede prevenirse. Una pesquisa correcta durante el embarazo y un adecuado control prenatal representan las únicas medidas para reducir la incidencia de la sífilis congénita.


Assuntos
Humanos , Feminino , Gravidez , Recém-Nascido , Diagnóstico Pré-Natal , Sífilis Congênita/diagnóstico , Sífilis Congênita/prevenção & controle , Sífilis Congênita/terapia , Transmissão Vertical de Doenças Infecciosas/prevenção & controle
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