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1.
Br J Dermatol ; 2024 May 13.
Artículo en Inglés | MEDLINE | ID: mdl-38735684

RESUMEN

BACKGROUND: Patients with lichen planus (LP) refractory to available therapies often experience a high disease burden; representing a population with a clear unmet need for new treatments. OBJECTIVES: To evaluate the efficacy and safety of secukinumab 300 mg over 32 weeks in adult patients with biopsy-proven cutaneous LP (CLP), mucosal LP (MLP) or lichen planopilaris (LPP), inadequately controlled by topical corticosteroids. METHODS: PRELUDE was a, randomised, double-blind, placebo-controlled, Phase 2 proof-of-concept study that enrolled patients with CLP, MLP or LPP. Eligible patients were randomised to eithersecukinumab 300 mg every 4 weeks for 32 weeks (SECQ4W), or placebo for 16 weeks followed by secukinumab 300 mg every 2 weeks (SECQ2W) for 16 weeks. The primary endpoint was achievement of the newly designed Investigator's Global Assessment (IGA) score ≤2 at Week 16. RESULTS: Overall, 111 patients were randomised (n=37 each) to CLP, MLP and LPP cohorts. As the proof-of-concept criteria were not met for any of the 3 cohorts, the primary objective was not met. A numerically higher proportion of patients achieved IGA ≤2 response at Week 16 with SECQ4W vs. placebo in the MLP (37.5% [95% credibility interval (Crl): 20.3-57.2] vs. 23.1% [95% Crl: 6.5-49.2]) and LPP cohorts (37.5% [95% Crl: 20.2-57.3] vs. 30.8% [95% Crl: 10.8-57.6]). In the LPP cohort, a sustained response for IGA ≤2 from Week 16 to Week 32 was achieved with SECQ4W (Week 16: 37.5%; Week 32: 45.8%), and a substantial improvement was observed in IGA ≤2 response in patients of this cohort switching from placebo (Week 16: 30.8%) to SECQ2W after Week 16 (Week 32: 63.6%). The safety profile was consistent with the known profile of secukinumab and showed no new or unexpected signals. CONCLUSIONS: PRELUDE is the first randomised controlled basket trial evaluating interleukin-17A inhibition with secukinumab across 3 subtypes of LP. Secukinumab was well-tolerated and safe, showing different response rates across the 3 subtypes, with numerical IGA improvements in MLP and LPP, and no response in CLP. The study raises the question of a differential role of interleukin-17A across LP subtypes. The novel IGA score showed significant correlation with patient as well as physician reported outcome measurements. TRIAL REGISTRATION NUMBER: NCT04300296.

2.
Pediatr Dermatol ; 34(2): e97-e98, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-28120347

RESUMEN

We report a case of an increasing number of discrete patches of darkly pigmented terminal hair in a patient with nevoid basal cell carcinoma syndrome. This case adds to a small case series of three patients which have previously reported this observation. We report this case to highlight hairy patches as an important clinical feature associated with nevoid basal cell carcinoma syndrome.


Asunto(s)
Síndrome del Nevo Basocelular/complicaciones , Síndrome del Nevo Basocelular/patología , Carcinoma Basocelular/complicaciones , Enfermedades del Cabello/etiología , Neoplasias Cutáneas/complicaciones , Adolescente , Carcinoma Basocelular/patología , Femenino , Humanos , Neoplasias Cutáneas/patología
3.
Dermatol Online J ; 23(5)2017 May 22.
Artículo en Inglés | MEDLINE | ID: mdl-28537874

RESUMEN

Application to dermatology residency is a highly competitive process. Although factors associated with successfully matching have been studied, less is known regarding the ability of admissions committees to screen applicants in a uniform manner or the importance of the interview in ranking applicants. Our goal was to retrospectively measure our admission committee evaluators' concordance regarding residency application credentials and interview performance, and ultimately the effects on final applicant ranking.


Asunto(s)
Dermatología/educación , Internado y Residencia , Entrevistas como Asunto , Selección de Personal/métodos , Evaluación Educacional , Competencia Profesional , Estudios Retrospectivos , Estados Unidos
4.
Dermatol Online J ; 23(12)2017 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-29447648

RESUMEN

BACKGROUND/AIMS: Limited data are available regarding the undergraduate dermatology clinical clerkship curriculum in the United States. Our primaryaim is to assess medical students' perspectives of the dermatology clinical clerkship. METHODS: A multicenter survey study was conducted, which included four California dermatology academic programs. A 17-item questionnaire was designed to investigate medical student perception with regard tothe overall educational value of the various teaching aspects of the dermatology clinical clerkship. RESULTS: A total of 152 medical student surveys were completed. Over half of the medical students felt proficient in diagnosing the most commondermatologic conditions. Eighty-seven percent of medical students were very satisfied with the dermatology clerkship. Ninety-one percent of students felt the length of the clerkship was appropriate. CONCLUSIONS: The vast majority of medical students reported a high level of proficiency in the treatment and diagnosis of common skin disorders. In contrast, our findings suggest that medical students may not begaining sufficient hands-on experience in conducting certain dermatologic procedures following the dermatology clerkship. Overall, medical studentperception of the dermatology clinical clerkship was mostly positive.


Asunto(s)
Prácticas Clínicas , Competencia Clínica , Dermatología/educación , Enfermedades de la Piel/diagnóstico , Estudiantes de Medicina , California , Curriculum , Educación de Pregrado en Medicina/métodos , Humanos , Encuestas y Cuestionarios
5.
Dermatol Online J ; 22(7)2016 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-27617720

RESUMEN

ImportanceThe dynamics of the medical care team, including interactions between physicians and nursing staff, has a large role to play in patient care, patient satisfaction, and future possible reimbursement determination. In order to implement changes to improve this dynamic within the medical team, it is imperative that appropriate assessments are completed to determine baseline satisfaction of our patients and nursing staff in addition to provider self-assessment.ObjectiveWe aimed to investigate patient and nursing staff satisfaction with regards to provider quality of care in an outpatient academic dermatology clinic setting. We also sought out to determine provider insight in regards to satisfaction of patient and nursing staff.MethodsOur nursing staff, patients, and providers completed a questionnaire. We then compared nursing satisfaction data and patient satisfaction data with provider self-assessment to determine provider self-awareness.ResultsA total of 23 provider and nurse surveys and 562 patient satisfaction surveys were completed. Paired comparison and descriptive statistics were utilized to compare patient satisfaction, nursing satisfaction, and provider self-assessments.ConclusionsOverall, the results of the surveys demonstrated that the nursing staff and patients had high satisfaction in their interactions with the dermatology physicians. The physicians had appropriate insight into how they were perceived by the nursing staff and patients. Attending physicians as compared to resident physicians and male physicians as compared to female physicians tended to underrate themselves.


Asunto(s)
Actitud del Personal de Salud , Enfermeras y Enfermeros , Satisfacción del Paciente , Relaciones Médico-Enfermero , Médicos , Calidad de la Atención de Salud , Autoevaluación (Psicología) , Rendimiento Laboral , Atención Ambulatoria , Competencia Clínica , Dermatología , Humanos , Personal de Enfermería , Grupo de Atención al Paciente , Encuestas y Cuestionarios
6.
Dermatol Online J ; 21(10)2015 Oct 16.
Artículo en Inglés | MEDLINE | ID: mdl-26632801

RESUMEN

Connective tissue diseases such as systemic lupus erythematosus (SLE), systemic sclerosis (SSc), and Sjögren syndrome (SS) have presented many difficulties both in their diagnosis and treatment. Known causes for this difficulty include uncertainty of disease etiology, the multitude of clinical presentations, the unpredictable disease course, and the variable cell types, soluble mediators, and tissue factors that are believed to play a role in the pathogenesis of connective tissue diseases. The characteristic oral findings seen with these specific connective tissue diseases may assist with more swift diagnostic capability. Additionally, the recent use of biologics may redefine the success rate in the treatment and management of the disease. In this review we describe the oral manifestations associated with SLE, SSc, and SS and review the novel biologic drugs used to treat these conditions.


Asunto(s)
Antiinflamatorios/uso terapéutico , Enfermedades del Tejido Conjuntivo/terapia , Manejo de la Enfermedad , Terapia de Inmunosupresión/métodos , Mucosa Bucal/patología , Enfermedades del Tejido Conjuntivo/diagnóstico , Humanos , Pronóstico
7.
ScientificWorldJournal ; 2014: 742826, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24672362

RESUMEN

Lichen planus (LP) is a chronic inflammatory disorder that most often affects middle-aged adults. LP can involve the skin or mucous membranes including the oral, vulvovaginal, esophageal, laryngeal, and conjunctival mucosa. It has different variants based on the morphology of the lesions and the site of involvement. The literature suggests that certain presentations of the disease such as esophageal or ophthalmological involvement are underdiagnosed. The burden of the disease is higher in some variants including hypertrophic LP and erosive oral LP, which may have a more chronic pattern. LP can significantly affect the quality of life of patients as well. Drugs or contact allergens can cause lichenoid reactions as the main differential diagnosis of LP. LP is a T-cell mediated immunologic disease but the responsible antigen remains unidentified. In this paper, we review the history, epidemiology, and clinical subtypes of LP. We also review the histopathologic aspects of the disease, differential diagnoses, immunopathogenesis, and the clinical and genetic correlations.


Asunto(s)
Liquen Plano/clasificación , Humanos , Liquen Plano/diagnóstico , Liquen Plano/patología , Pronóstico , Factores de Riesgo
8.
Sci Total Environ ; 797: 149034, 2021 Nov 25.
Artículo en Inglés | MEDLINE | ID: mdl-34303243

RESUMEN

Lake water level fluctuation is a function of hydro-meteorological components, namely input, and output to the system. The combination of these components from in-situ and remote sensing sources has been used in this study to define multiple scenarios, which are the major explanatory pathways to assess lake water levels. The goal is to analyze each scenario through the application of the water balance equation to simulate lake water levels. The largest lake in Iran, Lake Urmia, has been selected in this study as it needs a great deal of attention in terms of water management issues. We ran a monthly water balance simulation of nineteen scenarios for Lake Urmia from 2003 to 2007 by applying different combinations of data, including observed and remotely sensed water level, flow, evaporation, and rainfall. We used readily available water level data from Hydrosat, Hydroweb, and DAHITI platforms; evapotranspiration from MODIS and rainfall from TRMM. The analysis suggests that the consideration of field data in the algorithm as the initial water level can reproduce the fluctuation of Lake Urmia water level in the best way. The scenario that combines in-situ meteorological components is the closest match to the observed water level of Lake Urmia. Almost all scenarios showed good dynamics with the field water level, but we found that nine out of nineteen scenarios did not vary significantly in terms of dynamics. The results also reveal that, even without any field data, the proposed scenario, which consists entirely of remote sensing components, is capable of estimating water level fluctuation in a lake. The analysis also explains the necessity of using proper data sources to act on water regulations and managerial decisions to understand the temporal phenomenon not only for Lake Urmia but also for other lakes in semi-arid regions.


Asunto(s)
Monitoreo del Ambiente , Lagos , Clima Desértico , Irán , Agua
9.
Dermatol Ther ; 23(3): 230-42, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20597942

RESUMEN

Candidiasis, an often encountered oral disease, has been increasing in frequency. Most commonly caused by the overgrowth of Candida albicans, oral candidiasis can be divided into several categories including acute and chronic forms, and angular cheilitis. Risk factors for the development of oral candidiasis include immunosuppression, wearing of dentures, pharmacotherapeutics, smoking, infancy and old age, endocrine dysfunction, and decreased salivation. Oral candidiasis may be asymptomatic. More frequently, however, it is physically uncomfortable, and the patient may complain of burning mouth, dysgeusia, dysphagia, anorexia, and weight loss, leading to nutritional deficiency and impaired quality of life. A plethora of antifungal treatments are available. The overall prognosis of oral candidiasis is good, and rarely is the condition life threatening with invasive or recalcitrant disease.


Asunto(s)
Antifúngicos/administración & dosificación , Candidiasis Bucal/tratamiento farmacológico , Queilitis/microbiología , Administración Tópica , Candidiasis Bucal/clasificación , Candidiasis Bucal/diagnóstico , Queilitis/diagnóstico , Violeta de Genciana , Humanos , Fenazinas , Factores de Riesgo
10.
Dermatol Online J ; 16(4): 11, 2010 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-20409418

RESUMEN

Kaposi sarcoma (KS) may be categorized into four primary clinical variants: classic, iatrogenic, endemic or African, and epidemic or acquired immunodeficiency syndrome (AIDS)-related KS. Acquired immunodeficiency syndrome-associated Kaposi sarcoma typically presents on the face and trunk as pink to red macules and papules and can be rapidly progressive leading to disseminated visceral involvement and death. Rarely has AIDS-associated KS been described as presenting on the feet. We report a case of AIDS-associated nodular KS manifesting as an exophytic nodule on the plantar foot.


Asunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/diagnóstico , Enfermedades del Pie/diagnóstico , Sarcoma de Kaposi/diagnóstico , Infecciones Oportunistas Relacionadas con el SIDA/tratamiento farmacológico , Infecciones Oportunistas Relacionadas con el SIDA/patología , Adulto , Antibióticos Antineoplásicos/uso terapéutico , Terapia Antirretroviral Altamente Activa , Doxorrubicina/uso terapéutico , Enfermedades del Pie/tratamiento farmacológico , Enfermedades del Pie/patología , Humanos , Masculino , Sarcoma de Kaposi/tratamiento farmacológico , Sarcoma de Kaposi/patología
11.
Med Sci Educ ; 30(1): 315-321, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-34457673

RESUMEN

PURPOSE: Resident physician mistreatment and burnout are widespread issues in medical training, but the association between the two remains unclear. This study examines the prevalence and types of mistreatment among resident physicians in core specialties and its association with burnout syndrome as well as feelings of depression/anxiety. METHODS: A cross-sectional, survey-based observational study of medical residents was conducted at the University of California, Davis Medical Center in 2014. Current residents (PGY2 or higher) in the internal medicine, family medicine, obstetrics/gynecology, surgery, and pediatrics programs completed anonymous questionnaires addressing topics such as workplace mistreatment, feelings of depression/anxiety, and stress management. Burnout was measured using the Maslach Burnout Inventory. RESULTS: Forty-four out of 105 residents (41.9%) witnessed mistreatment of their co-residents while 26 residents (24.8%) disclosed personal accounts of mistreatment. Seventy-one percent of residents met the criteria for burnout. Residents who had been personally mistreated were almost eight times more likely to report burnout (OR 7.6, 95% CI = 1.7-34.4) and almost four times more likely to report symptoms of anxiety and depression (OR 3.8, 95% CI = 1.6-9.1). Public belittlement or humiliation was the most common type of mistreatment. CONCLUSION: Encountering mistreatment was associated with higher rates of burnout, as well as depression/anxiety. While it is uncertain if mistreatment in the workplace has a causative impact on burnout syndrome, the findings reveal the need to address work-related environmental factors that may contribute to both resident physician mistreatment and burnout.

12.
Curr Opin Gastroenterol ; 25(2): 136-43, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19528881

RESUMEN

PURPOSE OF REVIEW: Zinc plays an essential role in numerous biochemical pathways. Zinc deficiency affects many organ systems, including the integumentary, gastrointestinal, central nervous system, immune, skeletal, and reproductive systems. This article aims to discuss zinc metabolism and highlights a few of the diseases associated with zinc deficiency. RECENT FINDINGS: Zinc deficiency results in dysfunction of both humoral and cell-mediated immunity and increases the susceptibility to infection. Supplementation of zinc has been shown to reduce the incidence of infection as well as cellular damage from increased oxidative stress. Zinc deficiency is also associated with acute and chronic liver disease. Zinc supplementation protects against toxin-induced liver damage and is used as a therapy for hepatic encephalopathy in patients refractory to standard treatment. Zinc deficiency has also been implicated in diarrheal disease, and supplementation has been effective in both prophylaxis and treatment of acute diarrhea. SUMMARY: This article is not meant to review all of the disease states associated with zinc deficiency. Rather, it is an introduction to the influence of the many roles of zinc in the body, with an extensive discussion of the influence of zinc deficiency in selected diseases. Zinc supplementation may be beneficial as an adjunct to treatment of many disease states.


Asunto(s)
Zinc/deficiencia , Enfermedades Carenciales/complicaciones , Suplementos Dietéticos , Disentería/etiología , Humanos , Inmunidad , Mucosa Intestinal/metabolismo , Hepatopatías/etiología , Zinc/fisiología
13.
J Pediatr Adolesc Gynecol ; 32(1): 83-85, 2019 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-30244192

RESUMEN

BACKGROUND: Lichen sclerosus is a chronic inflammatory dermatological condition with a predilection for the anogenital area. CASE: We describe a case of iatrogenic Cushing syndrome from the administration of high-potency topical steroids for vulvar lichen sclerosus in a 6-year-old girl. Her symptoms resolved after the cessation of topical steroid treatment. SUMMARY AND CONCLUSION: This case brings attention to iatrogenic Cushing syndrome as a potential complication when using high-potency topical corticosteroids in the anogenital region.


Asunto(s)
Clobetasol/efectos adversos , Síndrome de Cushing/inducido químicamente , Glucocorticoides/efectos adversos , Liquen Escleroso Vulvar/tratamiento farmacológico , Administración Tópica , Niño , Clobetasol/administración & dosificación , Síndrome de Cushing/diagnóstico , Femenino , Glucocorticoides/administración & dosificación , Humanos
14.
Dermatol Online J ; 14(11): 7, 2008 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-19094845

RESUMEN

A 10-year-old boy with a history of tuberous sclerosis was sent for evaluation of numerous papules on his lower gum area. The parent was concerned that the lesions were interfering with oral hygiene. A diagnosis of oral fibromas was made and treatment options of gingivectomy or electrosurgery combined with carbon dioxide laser were described to the patient and his parent. Therapy with electrocautery and a pulsed carbon dioxide laser was decided on and utilized. We describe for the first time the combination of electrosurgery and carbon dioxide laser as a treatment method for oral fibromas. A short review of the literature regarding diagnosis and treatment is included with this report.


Asunto(s)
Angiofibroma/cirugía , Electrocoagulación , Neoplasias Gingivales/cirugía , Terapia por Láser , Esclerosis Tuberosa/cirugía , Angiofibroma/genética , Niño , Neoplasias Gingivales/genética , Humanos , Masculino , Esclerosis Tuberosa/genética
15.
Dermatol Nurs ; 20(2): 117-20, 2008 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-18549127

RESUMEN

Pseudoepitheliomatous, keratotic, and micaceous balanitis is a rare condition involving the skin of the glans penis that occurs in older men, most circumcised late in life. This condition is of uncertain malignant potential, and has been associated with progression to verrucous carcinoma and squamous cell carcinoma. The etiology of this condition is unknown. Treatment depends on severity, and may range from topical treatment to surgical excision.


Asunto(s)
Balanitis/patología , Lesiones Precancerosas/patología , Balanitis/terapia , Carcinoma de Células Escamosas/patología , Carcinoma Verrugoso/patología , Diagnóstico Diferencial , Humanos , Masculino , Persona de Mediana Edad , Neoplasias del Pene/patología
16.
J Am Acad Dermatol ; 57(3): 421-7, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17532096

RESUMEN

BACKGROUND: Erosive pustular dermatosis (EPD) is a rarely reported condition that primarily involves the actinically damaged scalp of elderly women. Although the condition is well recognized in the United Kingdom and Europe, no US cases have heretofore been reported. OBJECTIVES: We sought to document the presence, and determine the clinical characteristics, of EPD in the US population. METHODS: Patients were recruited from the dermatology clinic at a university in California and from the private practices of dermatologists in the Northern California region. RESULTS: Eleven patients with EPD were identified. Eight were women and 3 were men. The scalp was involved in 9 patients and the extremities in two patients. The involved skin was actinically damaged in 9 patients. The patients were elderly (66-90 years) but one patient was a 15-year-old boy. All lesions resolved or greatly improved with the application of high-potency steroids or tacrolimus. LIMITATIONS: Not all patients were examined personally by the authors of this article. The length of follow-up was relatively short. CONCLUSIONS: EPD is a fairly common disease and is the most likely diagnosis in instances where chronic, nonhealing, shallow erosions occur on actinically damaged, or otherwise atrophic, skin. In spite of the name, intact pustules are rarely present. The histology is that of moderate to marked, nonspecific chronic inflammation. EPD responds well to high-potency topical steroids.


Asunto(s)
Extremidades , Dermatosis del Cuero Cabelludo/patología , Enfermedades Cutáneas Vesiculoampollosas/patología , Enfermedades de la Piel/patología , Administración Tópica , Adolescente , Anciano , Anciano de 80 o más Años , Atrofia , Inhibidores de la Calcineurina , Clobetasol/administración & dosificación , Clobetasol/uso terapéutico , Femenino , Estudios de Seguimiento , Glucocorticoides/administración & dosificación , Glucocorticoides/uso terapéutico , Humanos , Masculino , Trastornos por Fotosensibilidad/complicaciones , Dermatosis del Cuero Cabelludo/tratamiento farmacológico , Enfermedades de la Piel/tratamiento farmacológico , Enfermedades de la Piel/etiología , Enfermedades Cutáneas Vesiculoampollosas/tratamiento farmacológico , Enfermedades Cutáneas Vesiculoampollosas/etiología , Esteroides/administración & dosificación , Esteroides/uso terapéutico , Tacrolimus/administración & dosificación , Tacrolimus/uso terapéutico , Resultado del Tratamiento
17.
J Am Acad Dermatol ; 56(1): 116-24, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17190629

RESUMEN

Acrodermatitis enteropathica is a rare autosomal recessive disorder of zinc deficiency. The genetic defect has been mapped to 8q24 and the defective gene identified as SLC39A4, which encodes the zinc transporter Zip4. The diagnosis is made by way of clinical presentation together with histopathology and laboratory tests. Here we provide an overview of zinc metabolism and a description of inherited and acquired zinc deficiency.


Asunto(s)
Acrodermatitis/genética , Proteínas de Transporte de Catión/deficiencia , Síndromes de Malabsorción/genética , Zinc/deficiencia , Acrodermatitis/diagnóstico , Acrodermatitis/epidemiología , Acrodermatitis/metabolismo , Adulto , Animales , Proteínas de Transporte de Catión/química , Proteínas de Transporte de Catión/genética , Proteínas de Transporte de Catión/fisiología , Dieta , Modelos Animales de Enfermedad , Femenino , Regulación de la Expresión Génica , Genes Recesivos , Humanos , Lactante , Absorción Intestinal , Mucosa Intestinal/metabolismo , Yeyuno/metabolismo , Síndromes de Malabsorción/diagnóstico , Síndromes de Malabsorción/epidemiología , Síndromes de Malabsorción/metabolismo , Masculino , Ratones , Ratones Mutantes , Leche/química , Necesidades Nutricionales , Piel/patología , Zinc/metabolismo , Zinc/farmacocinética , Zinc/fisiología , Zinc/uso terapéutico
18.
Dermatol Online J ; 13(3): 11, 2007 Jul 13.
Artículo en Inglés | MEDLINE | ID: mdl-18328205

RESUMEN

A 13-year-old girl presented with a history of red scaly plaques involving the chest, arms and legs beginning in infancy. Punch biopsy revealed psoriasiform hyperplasia and pallor of the epidermis. The patient's serum zinc level was 36 mug/dl [nl. 66-144 mug/dl]. A diagnosis of acrodermatitis enteropathica was established and the patient responded well to zinc replacement therapy. Acrodermatitis enteropathica is a rare autosomal recessive disorder caused by mutations in SLC39A4, which encodes the tissue-specific zinc transporter ZIP4.


Asunto(s)
Acrodermatitis/genética , Proteínas de Transporte de Catión/genética , Mutación , Sulfato de Zinc/uso terapéutico , Zinc/deficiencia , Acrodermatitis/diagnóstico , Acrodermatitis/tratamiento farmacológico , Adolescente , Astringentes/uso terapéutico , Biopsia , Proteínas de Transporte de Catión/metabolismo , Diagnóstico Diferencial , Femenino , Estudios de Seguimiento , Predisposición Genética a la Enfermedad , Humanos , Piel/metabolismo , Piel/patología , Zinc/sangre
19.
Clin Dermatol ; 35(5): 453-460, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28916026

RESUMEN

Primary burning mouth syndrome (BMS) is an oral mucosal disorder that is characterized by a chronic and often debilitating intraoral burning sensation for which no localized or systemic cause can be found. BMS most commonly affects postmenopausal women. The pathophysiology of primary BMS is not well understood. Diagnosing BMS can prove to be challenging. BMS patients can also pose a therapeutic challenge to clinicians who are consulted to evaluate these patients. Most commonly used therapies include tricyclic antidepressants, α-lipoic acid, clonazepam, and cognitive-behavioral therapy. Clinical judgment, patient counseling, and monitoring of pain are important. Further research is required to assess the effectiveness of serotonin and newer serotonin-noradrenalin reuptake inhibitors.


Asunto(s)
Síndrome de Boca Ardiente/diagnóstico , Síndrome de Boca Ardiente/terapia , Antidepresivos Tricíclicos/uso terapéutico , Antioxidantes/uso terapéutico , Clonazepam/uso terapéutico , Terapia Cognitivo-Conductual , Femenino , Moduladores del GABA/uso terapéutico , Humanos , Ácido Tióctico/uso terapéutico
20.
Clin Dermatol ; 35(5): 477-483, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28916029

RESUMEN

Although the surfaces of both the skin and oral mucosa are protected by squamous epithelial cells and fall within the scope of dermatologic practice, the oral cavity contains highly specialized structures and functions distinct from other skin biology and pathologic conditions and are also the purview of clinicians who care for patients with skin and mucosal diseases. We describe the distinct features of the tongue, mucosa, and salivary glands. In particular, we examine the composition and function of the saliva, with special focus on salivary biomarkers. Within the oral cavity, saliva shows great promise as a noninvasive and sensitive marker for many systemic diseases. Biomarkers are being used as diagnostic or monitoring tools for a wide variety of diseases, including systemic lupus erythematosus, Sjögren disease, Behçet disease, and autoimmune blistering disorders, as well as premalignant and malignant lesions of the mouth.


Asunto(s)
Mucosa Bucal/fisiología , Saliva/química , Saliva/fisiología , Enfermedades Autoinmunes , Síndrome de Behçet/diagnóstico , Biomarcadores/análisis , Vesícula/diagnóstico , Vesícula/inmunología , Humanos , Lupus Eritematoso Sistémico/diagnóstico , Mucosa Bucal/anatomía & histología , Glándulas Salivales/anatomía & histología , Glándulas Salivales/fisiología , Síndrome de Sjögren/diagnóstico , Lengua/anatomía & histología , Lengua/fisiología
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