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4.
J Drugs Dermatol ; 13(4): 444-8, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24719064

RESUMO

BACKGROUND: Melasma has a negative impact on quality of life since it typically occurs on the face. OBJECTIVES: To evaluate the erythema and pigmentation of melasma lesions and the surrounding areas in patients receiving triple combination (TC: hydroquinone, tretinoin, and fluocinolone acetonide) regimens. METHODS: Patients first received an 8-week daily TC treatment and were then randomized to twice weekly or tapering regimen with TC. Melanin and erythema levels of lesions and surrounding areas were objectively measured using a narrowband reflectance spectrophotometer. RESULTS: Progressive reduction in the mean melanin levels was observed in the treatment phase. Following both maintenance regimens, there was no difference between melanin levels in the melasma lesions. Adverse effects were rare in both phases of the study and there was borderline reduction in erythema with regimen II. CONCLUSION: Both maintenance regimens were effective in maintaining results obtained during the initial treatment phase, and were safe and well-tolerated. Erythema was less intense with the tapering regimen.


Assuntos
Eritema/patologia , Melanose/tratamento farmacológico , Melanose/patologia , Pigmentação da Pele , Adolescente , Adulto , Anti-Inflamatórios/administração & dosagem , Antioxidantes/administração & dosagem , Quimioterapia Combinada/efeitos adversos , Fluocinolona Acetonida/administração & dosagem , Humanos , Hidroquinonas/administração & dosagem , Ceratolíticos/administração & dosagem , Assistência de Longa Duração , Quimioterapia de Manutenção/efeitos adversos , Melaninas/metabolismo , Melanose/metabolismo , Estudos Prospectivos , Método Simples-Cego , Pele/patologia , Tretinoína/administração & dosagem , Adulto Jovem
5.
J Dtsch Dermatol Ges ; 12(3): 237-42, 237-43, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24533826

RESUMO

BACKGROUND: Epidermolysis bullosa (EB) nevi are acquired pigmented melanocytic lesions which may have clinical and dermoscopic features quite similar to those found in melanoma. More detailed information on this phenomenon is still lacking. OBJECTIVES: To evaluate clinical, dermoscopic, and histopathological features of melanocytic lesions in 13 patients with dystrophic EB (DEB). PATIENTS AND METHODS: Patients underwent clinical and dermoscopic evaluation. Suspicious lesions were excised and examined microscopically. RESULTS: There were 12 cases of recessive DEB and one of dominant DEB. Five patients were men; 8 were women; the ages ranged from 2 to 27 years old. All patients had at least 2 atypical melanocytic lesions. Two of the 5 biopsied patients showed an atypical nevus or lentigo on histopathological examination. CONCLUSIONS: We observed a high incidence of large and atypical melanocytic lesions in DEB patients. Although the exact explanation for this is still unclear, it seems that re-epithelization and the chronic inflammatory process may stimulate the proliferation of melanocytes, as well as the emergence of lesions with atypical clinical and dermoscopic features. As an unequivocal discrimination from malignant melanoma in vivo is not always possible, regular clinical follow-up and histopathological evaluation of suspicious lesions in EB patients are mandatory.


Assuntos
Dermoscopia , Epidermólise Bolhosa Distrófica/diagnóstico , Nevo Pigmentado/diagnóstico , Neoplasias Cutâneas/diagnóstico , Pele/patologia , Adolescente , Adulto , Criança , Pré-Escolar , Epidermólise Bolhosa Distrófica/complicações , Feminino , Humanos , Masculino , Nevo Pigmentado/etiologia , Neoplasias Cutâneas/etiologia , Adulto Jovem
6.
JMIR Form Res ; 8: e49616, 2024 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-38300698

RESUMO

BACKGROUND: Novel internet-based applications and associated technologies have influenced all aspects of society, ranging from commerce and business to entertainment and health care, and education is no exception. In this context, this study was designed to evaluate the impact of a dermatology e-learning program on the academic performance of medical students in dermatology. OBJECTIVE: The aim of this study is to develop a dermatology blended-learning course for undergraduate medical students, evaluate the knowledge gained by students exposed to this course, and compare the results to those of traditional teaching methods. METHODS: In this prospective study, we evaluated the performance of fourth-semester medical students at the Federal University of Bahia, Brazil. Students who had been in their second year of the medical course in 2019 were considered the control group, while students in their second year in 2020 were considered the blended or hybrid group. The first group attended traditional classes, using printed material (books and handouts), while the second group used our web-based course and e-book as a supplement in a hybrid web-plus-traditional fashion. Neither participants nor evaluators were blinded. The students in both groups were subjected to the same pre- and postcourse face-to-face, multiple-choice, paper-based evaluations, and we compared their performances. The content of the classes was the same for both groups. All didactic activities were developed by a team of certified dermatologists and professors from the university. RESULTS: A total of 129 students were selected and divided into 2 groups: the control group (n=57) and the hybrid group (n=72). The precourse tests did not indicate any difference between the control group (mean score 2.74, SD 1.25) and the hybrid group (mean score 3.2, SD 1.22 SD; P>.05). The hybrid group had better final-term grades (mean 8.18, SD 1.26) than the traditional group (mean 7.11, SD 1.04). This difference was statistically significant (P<.05). CONCLUSIONS: This study explores pedagogical possibilities in the field of dermatology teaching for medical school students. The results suggest that the performance of undergraduate students who attended the course with additional e-learning material was superior when compared to the performance of those who participated in the traditional course alone.

7.
Am J Dermatopathol ; 35(5): 541-54, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23715077

RESUMO

Primary oral mucosal melanoma is a rare aggressive tumor. Recent studies have demonstrated a correlation between increased tumor invasion and the metastatic phenotype and altered adhesion molecule expression profiles. The present study analyzed the expression of integrins, claudins, and immunoglobulin-like adhesion molecules in oral mucosal melanomas and correlated results with clinical parameters. Immunohistochemical analyses of the expression patterns of these molecules were performed on thirty-five cases of primary oral mucosal melanomas organized in a tissue microarray. The results were correlated with clinical and histological features of the cohort. A number of integrin subunits were negative and this was related with vascular invasion. Positivity of integrin beta-3 and CD166 (activated leukocyte cell adhesion molecule) was statistically associated with extensive vascular invasion (P < 0.05). Lower expression of CD54 (intercellular cell adhesion molecule) was associated with cases with extensive necrosis. Most cases with metastatic disease were negative for CD66 (carcinoembryonic antigen-related cell adhesion molecule). Several subunits of claudins were negative and, although not statistically significant, this lack of expression was partially associated with histological factors of poor prognosis. Altered patterns of adhesion molecule expression, mainly integrins and immunoglobulin-like proteins, may participate in the pathogenesis and outcome of oral mucosal melanomas.


Assuntos
Biomarcadores Tumorais/análise , Moléculas de Adesão Celular/análise , Claudinas/análise , Imunoglobulinas/análise , Integrinas/análise , Melanoma/química , Mucosa Bucal/química , Neoplasias Bucais/química , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Biópsia , Bolívia , Brasil , Distribuição de Qui-Quadrado , Criança , Pré-Escolar , Feminino , Humanos , Imuno-Histoquímica , Lactente , Recém-Nascido , Masculino , Melanoma/secundário , Pessoa de Meia-Idade , Mucosa Bucal/patologia , Neoplasias Bucais/patologia , Necrose , Gradação de Tumores , Invasividade Neoplásica , Prognóstico , Análise Serial de Tecidos , Adulto Jovem
10.
Rev Assoc Med Bras (1992) ; 67(1): 77-82, 2021 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-34161467

RESUMO

OBJECTIVE: Oculocutaneous albinism describes a group of pigmentary disorders that lead to skin sensitivity and predisposition to skin malignances. AIMS: To analyze clinical and epidemiological data in oculocutaneous albinism patients and to determine the prevalence of malignant skin lesions, assessing possible risk factors for skin cancer. METHODS: Cross-sectional study evaluating epidemiological data, habits of sun exposure and sun protection, and clinical examination of albino patients followed in a reference dermatology outpatient clinic in Brasil. Our primary outcome was the occurrence of malignant skin lesions in biopsied tissues. RESULTS: Of 74 patients analyzed, 11 (15%) had one or more suspicious lesions and were biopsied, of which 8 (72.7%) patients presented with basal cell carcinomas, 7 (63.3%) presented with squamous cell carcinoma, and 1 (9%) presented with melanoma. Moreover, 32(43%) patients presented with actinic keratosis. Age, female gender, previous history of sunburn, history of malignant lesions and history of sun exposure without photoprotection were associated with the presence of malignant lesions. LIMITATIONS: Unicentric, non-aleatory sample. CONCLUSIONS: There was a high prevalence of malignant and pre-malignant lesions in this population. Some potentially modifiable risk factors were associated with the occurrence of malignant skin lesions.


Assuntos
Albinismo Oculocutâneo , Neoplasias Cutâneas , Queimadura Solar , Albinismo Oculocutâneo/epidemiologia , Brasil/epidemiologia , Estudos Transversais , Feminino , Humanos , Prevalência , Neoplasias Cutâneas/epidemiologia , Queimadura Solar/complicações , Queimadura Solar/epidemiologia
11.
J Cutan Pathol ; 37(4): 432-8, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19614726

RESUMO

BACKGROUND: Xerostomia is a symptom that can be triggered by chronic diseases such as Sjögren's syndrome (SS) and lupus erythematosus (LE). Many authors regard most cases of salivary hypofunction in LE to secondary SS. Others believe that salivary changes in patients with LE might reflect a multisystem presentation of the disease. The present study compared histopathological and direct immunofluorescence (DIF) alterations in salivary glands of patients with xerostomia and diagnosis of LE or SS. METHODS: Twenty-eight salivary gland biopsies from patients with xerostomia and diagnosed with LE or SS were submitted to histopathological and DIF exams. RESULTS: From the 28 patients, 16 had SS and 12 had LE. In SS, a moderate to intense sialadenitis was detected, with infiltration and destruction of excretory salivary ducts. In LE, mild/moderate sialadenitis with thickening and hyalinization of the ductal basement membrane was observed. DIF revealed that 50% of SS patients presented intercellular ductal IgA deposits, whereas 58% of LE patients showed deposits of IgG in the ductal basement membrane. CONCLUSIONS: Alterations in salivary glands of LE patients may be a specific manifestation of the disease (lupus sialadenitis), reflecting its multisystemic presentation, instead of an association of secondary SS and LE.


Assuntos
Lúpus Eritematoso Sistêmico/metabolismo , Glândulas Salivares Menores/metabolismo , Síndrome de Sjogren/metabolismo , Xerostomia/metabolismo , Adulto , Idoso , Feminino , Imunofluorescência , Humanos , Imunoglobulina A/metabolismo , Lúpus Eritematoso Sistêmico/complicações , Lúpus Eritematoso Sistêmico/patologia , Masculino , Pessoa de Meia-Idade , Glândulas Salivares Menores/patologia , Sialadenite/complicações , Sialadenite/metabolismo , Sialadenite/patologia , Síndrome de Sjogren/complicações , Síndrome de Sjogren/patologia , Xerostomia/complicações , Xerostomia/patologia
12.
Pediatr Dermatol ; 27(5): 453-8, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20561241

RESUMO

Ichthyosis is a heterogeneous cornification disorder. Melanocytic lesions have not been previously described in association with ichthyosis. Their clinical importance lies in the fact that they may simulate melanoma clinically and dermoscopically, as seen in epidermolysis bullosa. The objective of this study was to evaluate the clinical, dermoscopic, and histopathologic features of nevi and lentigines in 16 patients with autosomal recessive congenital ichthyosis-lamellar ichthyosis and nonbullous ichthyosiform congenital erythroderma. Patients underwent general clinical examination dermoscopy. The more suspicious lesions were excised and to histopathologic examination. Most patients (n = 13) reported no personal or familial history of melanoma or atypical nevi. All of the patients had at least five atypical melanocytic lesions. Ten of the 16 patients had at least one atypical nevus or lentigo. This study suggests that increased atypical melanocytic nevi may be a feature of long-standing congenital ichthyoses. Whether this finding is disease-related or a coincidental observation is difficult to ascertain. As an unequivocal discrimination from malignant melanoma in vivo is not always possible, regular clinical follow-up of patients with ichthyosis and increased or unusual nevi is recommended.


Assuntos
Ictiose/epidemiologia , Ictiose/patologia , Nevo Pigmentado/epidemiologia , Nevo Pigmentado/patologia , Adolescente , Adulto , Biópsia , Brasil/epidemiologia , Criança , Feminino , Humanos , Ictiose/genética , Incidência , Lentigo/epidemiologia , Lentigo/patologia , Masculino , Adulto Jovem
13.
Histol Histopathol ; 35(8): 911-917, 2020 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-32364615

RESUMO

INTRODUCTION: Hair follicles are produced in a cyclical manner and the machinery involved in the reproduction of these follicles is present since the fetal stage. Although extensive research has been done on the human hair follicle, very little is known about the importance of adhesion molecules in its development. MATERIAL AND METHODS: We analyzed here, the immunoexpression of beta-1 integrin, p-cadherin, e-cadherin, and beta-catenin in hair follicles from 26 formalin-fixed and paraffin-embedded skin samples from human embryos and fetus between 12-23 weeks of gestational age. RESULTS: The adhesion molecules beta-1 integrin and e-cadherin/p-cadherin were expressed from 12 weeks and seemed to play a role in regulating epidermis invagination. Beta-catenin immunostaining was negative in all cases; down regulation of this protein may be necessary for fetal hair development and thus facilitating hair follicle down growth. DISCUSSION/CONCLUSION: Adhesion molecules are essential for hair follicle down growth and proliferation; integrins and cadherins play a major role in this process. More studies are needed to describe hair follicle development.


Assuntos
Moléculas de Adesão Celular/análise , Folículo Piloso/embriologia , Moléculas de Adesão Celular/metabolismo , Feminino , Feto , Humanos , Masculino , Estudos Retrospectivos
14.
An Bras Dermatol ; 95(3): 278-282, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32299738

RESUMO

BACKGROUND: The hair follicle is a unique structure, one of the most dynamic structures in mammalians, which can reproduce in every new cycle all the mechanism involved in its fetal development. Although a lot of research has been made about the human hair follicle much less has been discovered about the importance of the cytokeratins (CKs) in its development. OBJECTIVE: Study the immunohistochemical pattern of epithelial CKs during human hair follicle development. METHODS: We performed an immunohistochemical study using fresh post-mortem skin biopsies of human fetuses between 4 and 25 weeks of gestational age to study the expression of cytokeratins (CKs): CK1, CK10, CK13, CK14, CK16 and CK20 during human hair follicle fetal development. STUDY LIMITATIONS: Restrospective study with a good number of makers but with a small population. RESULTS/CONCLUSION: We found that, the CKs were expressed in an intermediate time during follicular development. The epithelial CKs (CK1, CK14, CK10, CK13) and the epithelial CKs with a proliferative character such as CK16 were expressed first, as markers of cellular maturation and follicular keratinization. At a later phase, CK20 was expressed in more developed primitive hair follicles as previously discussed in literature.


Assuntos
Folículo Piloso/citologia , Folículo Piloso/crescimento & desenvolvimento , Queratinas Específicas do Cabelo/análise , Fatores Etários , Anticorpos Monoclonais/análise , Desenvolvimento Fetal , Idade Gestacional , Humanos , Imuno-Histoquímica , Estudos Retrospectivos
17.
J Cutan Pathol ; 35(8): 731-7, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-18430044

RESUMO

BACKGROUND: Cadherins and integrins are important for maintenance of tissue integrity and in signal transduction during skin development. Distribution of these molecules in human skin development was investigated and associated with markers of differentiation, cytokeratins (CK) and involucrin (INV). METHODS: Using immunohistochemistry expression of E- and P-cadherins, integrins beta-1 and -4, CK10, CK14 and INV was assessed in skin fragments of 10 human fetuses (gestational weeks ranged from 4 to 24, all weighing up to 500 g). RESULTS: At initial phases of development, integrins beta-1 and -4 and E- and P-cadherins were present on epithelial cell membranes in all layers. CK14 and CK10 were expressed in all epithelial layers and INV weakly detected in the superficial layer. In more advanced stages, integrins were detected in all layers, but a marked polarized expression was seen in basal layer. E-cadherin was detected in all layers, but the cornified stratum and P-cadherin were observed in the lower layers. CK14 was expressed in basal layer, CK10 in suprabasal stratum and INV was observed in cornified layer. CONCLUSIONS: Cadherins and integrins are essential for skin development, being spatially and temporally regulated. Their expression is related with the expression of maturation markers of the epidermis.


Assuntos
Antígenos de Diferenciação/biossíntese , Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Pele/embriologia , Caderinas/biossíntese , Epitélio/embriologia , Humanos , Integrinas/biossíntese , Queratinas/biossíntese , Precursores de Proteínas/biossíntese , Pele/citologia
19.
Rev. Assoc. Med. Bras. (1992, Impr.) ; 67(1): 77-82, Jan. 2021. tab
Artigo em Inglês | LILACS | ID: biblio-1287793

RESUMO

SUMMARY OBJECTIVE: Oculocutaneous albinism describes a group of pigmentary disorders that lead to skin sensitivity and predisposition to skin malignances. Aims: To analyze clinical and epidemiological data in oculocutaneous albinism patients and to determine the prevalence of malignant skin lesions, assessing possible risk factors for skin cancer. METHODS: Cross-sectional study evaluating epidemiological data, habits of sun exposure and sun protection, and clinical examination of albino patients followed in a reference dermatology outpatient clinic in Brasil. Our primary outcome was the occurrence of malignant skin lesions in biopsied tissues. RESULTS: Of 74 patients analyzed, 11 (15%) had one or more suspicious lesions and were biopsied, of which 8 (72.7%) patients presented with basal cell carcinomas, 7 (63.3%) presented with squamous cell carcinoma, and 1 (9%) presented with melanoma. Moreover, 32(43%) patients presented with actinic keratosis. Age, female gender, previous history of sunburn, history of malignant lesions and history of sun exposure without photoprotection were associated with the presence of malignant lesions. Limitations: Unicentric, non-aleatory sample. CONCLUSIONS: There was a high prevalence of malignant and pre-malignant lesions in this population. Some potentially modifiable risk factors were associated with the occurrence of malignant skin lesions.


Assuntos
Humanos , Feminino , Neoplasias Cutâneas/epidemiologia , Queimadura Solar/complicações , Queimadura Solar/epidemiologia , Albinismo Oculocutâneo/epidemiologia , Brasil/epidemiologia , Prevalência , Estudos Transversais
20.
An Bras Dermatol ; 86(4): 633-41; quiz 642-3, 2011.
Artigo em Inglês, Português | MEDLINE | ID: mdl-21987126

RESUMO

Oral lichen planus (OLP) is a relatively common mucosal disease that can present isolated or associated with cutaneous lichen planus. Contrarily to its cutaneous counterpart, though, OLP tends to be chronic, relapsing, and difficult to treat. Severe morbidity is related to erosive forms, and more aggressive presentations have been described, such as the "gingivo-vulvar syndrome". This article reviews the current knowledge about the pathogenesis, clinical picture, differential and laboratorial diagnosis, prognosis, and treatment of OLP.


Assuntos
Líquen Plano Bucal , Diagnóstico Diferencial , Humanos , Líquen Plano Bucal/classificação , Líquen Plano Bucal/tratamento farmacológico , Líquen Plano Bucal/etiologia , Líquen Plano Bucal/patologia , Prognóstico
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