Medicina cutanea ibero-latino-americana最新文献

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[Cutaneo-mucous precancer, treatment using CO2 laser]. 【皮肤-粘液癌前期,CO2激光治疗】。
J L Cisneros, R Singla, F Oliveras, M Martí
{"title":"[Cutaneo-mucous precancer, treatment using CO2 laser].","authors":"J L Cisneros,&nbsp;R Singla,&nbsp;F Oliveras,&nbsp;M Martí","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>It indicates the methodologic in work and study, that the compose 51 patients constituted for 20 cases with queratomas, 10 of cheilitis, 13 of leucoplasias and 8 of melanosis precancerous of Dubreuilh. Immediately, it described the fundamentals of the laser carbon dioxide its bases parametrica in the treatment especially for those pathologic precancerous of the skin and the results obtained, with its advantages and disadvantages.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 1","pages":"23-9"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13275553","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Poikiloderma congenitale of the Kindler type associated with multiple seborrheic warts]. [与多发脂溢性疣相关的Kindler型先天性千皮病]。
R A De Mattos, J A Sittart, N Y Valente
{"title":"[Poikiloderma congenitale of the Kindler type associated with multiple seborrheic warts].","authors":"R A De Mattos,&nbsp;J A Sittart,&nbsp;N Y Valente","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>A case an eleven year old girl with congenital poikiloderma, generalized xerosis and cutaneous atrophy, recurrent blister in extremities, sclerosis of the fingers and toes diffuse hyperkeratosis of palms and soles and webbing between some toes is reported here. Multiple seborrheic keratosis were also found, an association hitherto not mentioned with congenital poikiloderma.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 4","pages":"232-7"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13304765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Intranasal trichofolliculoma]. [鼻腔毛毛囊瘤]。
M D Arias Palomo, M C Gutierrez Ortega, A Hasson Nisis, L Martin Moreno, L Requena Caballero, A Barat Cascante, A Castro Torres
{"title":"[Intranasal trichofolliculoma].","authors":"M D Arias Palomo,&nbsp;M C Gutierrez Ortega,&nbsp;A Hasson Nisis,&nbsp;L Martin Moreno,&nbsp;L Requena Caballero,&nbsp;A Barat Cascante,&nbsp;A Castro Torres","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Trichofolliculoma is a rare benign neoplasm originated from hair follicle. Although this tumor often shows a suggestive clinical appearance, an accurate diagnosis only can be established by histopathologic findings. We report a case of intranasal trichofolliculoma. To the best of our knowledge, trichofolliculoma has not been previously described in this location.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 3","pages":"159-61"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13414237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Amelanotic melanoma. Study of 18 cases]. (无黑色素的黑色素瘤。[18例分析]。
M S Rutowitsch, R Garrido Neves, O Ferreira De Castro
{"title":"[Amelanotic melanoma. Study of 18 cases].","authors":"M S Rutowitsch,&nbsp;R Garrido Neves,&nbsp;O Ferreira De Castro","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The authors analyze a retrospective study of 18 cases of amelanotic melanoma, coming from 7 Departments of Dermatopathology, and 3 from private clinics in Brazil, during the period from 1980 through 1987. Nine of the 18 patients were men, and seven were women; 14 of the 18 were caucasian and 2 were blacks. Their average combined age was 56 years, varying from 24 years to 86 years. The average size of the lesions was 2.7 cm. and the location was: extremities = 7, thoracic wall = 5, upper limb = 2, and lower limb = 2. Only 2 cases included in this analyses, didn't have any other additional information about color, age, sex and location. The authors found that amelanotic melanoma is rare, in accordance with the literature. They point out, that the rarity or the lack of the melanic pigment within the tumors cells, makes the clinical diagnosis much more complex.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 1","pages":"49-57"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13367688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Apocrine nevus]. [顶泌痣]。
N Perez-Oliva, L J del Pozo Hernando, J A Tejerina, P A Quiñones
{"title":"[Apocrine nevus].","authors":"N Perez-Oliva,&nbsp;L J del Pozo Hernando,&nbsp;J A Tejerina,&nbsp;P A Quiñones","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>We present the case of a 32-year-old woman with a congenital lesion on her left cheek that histopathologically was composed of numerous mature apocrine glands. The diagnosis of pure apocrine nevus, a rare lesion of that our case probably represents the sixth described in the literature, was made.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 1","pages":"67-9"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13367692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Pedal papules in newborn infants]. [新生儿脚部丘疹]。
M Larralde de Luna, J Ruiz León, H N Cabrera
{"title":"[Pedal papules in newborn infants].","authors":"M Larralde de Luna,&nbsp;J Ruiz León,&nbsp;H N Cabrera","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Four cases of newborn children who presented pedal papules since birth, are reported. They showed the following features, different from the ones seen in adults: a solitary lesion, bigger size, localization on medial plantar region aspect of the heel, presence at birth, absence of an obvious piezogenic factor, physiopathogenic model that explains the development of lesions in adults, which are compared to those appearing in the newborn, are proposed.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 1","pages":"9-12"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13367694","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Polyarteritis nodosa. Considerations on a clinical case]. 结节性多动脉炎。对一个临床病例的思考]。
G M Pinto, O Farinha, F A Pacheco
{"title":"[Polyarteritis nodosa. Considerations on a clinical case].","authors":"G M Pinto,&nbsp;O Farinha,&nbsp;F A Pacheco","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>A case of polyarteritis nodosa is reported. The patient, a 56-year-old white woman, had cutaneous nodules, ulcers and livedo reticularis over the limbs. Abdominal angiography revealed the presence of microaneurysms. Hypertension, rheumatic heart disease (under anticoagulation therapy) and diabetes mellitus, were also detected. The controversial attempt in distinguishing between systemic and cutaneous polyarteritis is emphasized, and the influence of warfarin on skin lesions morphology is discussed.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 4","pages":"273-7"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13138641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Recurrent intertrigo as initial manifestation of histiocytosis X]. 【复发性三间肌是组织细胞增多症X的初始表现】。
P Sánchez-Pedreño, J C Moreno, F Camacho, J García Boitia, J González-Hachero
{"title":"[Recurrent intertrigo as initial manifestation of histiocytosis X].","authors":"P Sánchez-Pedreño,&nbsp;J C Moreno,&nbsp;F Camacho,&nbsp;J García Boitia,&nbsp;J González-Hachero","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Letterer-Siwe disease is the acute and usually fatal form of histiocytosis X. We describe here a patient with this process, which serves as a reminder of the presenting features of histiocytosis X.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 1","pages":"40-3"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13367687","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Skin and ungual pigmentation caused by ftorafur]. [因脚癣引起的皮肤和足部色素沉着]。
L J Del Pozo, J Vilella, M Jimeno, V Del Villar, M Asensio
{"title":"[Skin and ungual pigmentation caused by ftorafur].","authors":"L J Del Pozo,&nbsp;J Vilella,&nbsp;M Jimeno,&nbsp;V Del Villar,&nbsp;M Asensio","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>We report the case of a sixty-seven-years-old male diagnosed of a gastric adenocarcinoma that presented brown pigmentation in the dorsal of his both hands and fingernails while being on treatment with ftorafur, an analogous of 5-fluorouracil. To our knowledge this side effect has not been previously reported for ftorafur.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 1","pages":"78-80"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13367693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Flagellated pigmentation caused by bleomycin. Presentation of 2 cases]. 博来霉素引起的鞭毛状色素沉着。报告2例]。
M A Vicente, P Iranzo, A Azon, J M Mascaro, J Grau
{"title":"[Flagellated pigmentation caused by bleomycin. Presentation of 2 cases].","authors":"M A Vicente,&nbsp;P Iranzo,&nbsp;A Azon,&nbsp;J M Mascaro,&nbsp;J Grau","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Bleomycin may produce an unusual characteristic cutaneous manifestation: flagellate pigmentation. We present 2 patients, who received bleomycin for treatment of oral carcinoma and AIDS-associated Kaposi's sarcoma respectively, developing such pigmented flagellate streaks.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 2","pages":"148-50"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12864225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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