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[PMID]: 29182000 [Au] Autor: Beattie G; Tai C; Pinar Karakas S; Cham E; Idowu O; Kim S [Ad] Endereço: Department of Surgery, University of California San Francisco-East Bay Oakland, CA United States. [Ti] Título: Colossal pilomatrixoma. [So] Source: Ann R Coll Surg Engl;100(2):e38-e40, 2018 Feb. [Is] ISSN: 1478-7083 [Cp] País de publicação: England [La] Idioma: eng [Ab] Resumo: We describe the largest reported case of pilomatrixoma in the literature. While pilomatrixomas typically present as small soft-tissue nodules of the head, neck and upper extremities, they can also present as much larger masses in atypical locations. When they present in their usual size, pilomatrixomas have typical imaging features and can be correctly diagnosed with imaging studies before histological confirmation. Their clinical and imaging diagnosis become challenging when they are very large, as in our case. A giant pilomatrixoma should also be considered for paediatric patients presenting with a large subcutaneous soft-tissue mass. [Mh] Termos MeSH primário: Dorso Doenças do Cabelo Pilomatrixoma Neoplasias Cutâneas [Mh] Termos MeSH secundário: Adolescente Dorso/patologia Dorso/cirurgia Doenças do Cabelo/diagnóstico Doenças do Cabelo/patologia Doenças do Cabelo/cirurgia Seres Humanos Masculino Pilomatrixoma/diagnóstico Pilomatrixoma/patologia Pilomatrixoma/cirurgia Pele/patologia Neoplasias Cutâneas/diagnóstico Neoplasias Cutâneas/patologia Neoplasias Cutâneas/cirurgia [Pt] Tipo de publicação: CASE REPORTS; JOURNAL ARTICLE [Em] Mês de entrada: 1802 [Cu] Atualização por classe: 180209 [Lr] Data última revisão: 180209 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 171129 [St] Status: MEDLINE [do] DOI: 10.1308/rcsann.2017.0196

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[PMID]: 29369180 [Au] Autor: Abed K; Stopa Z; Siewert-Gutowska M [Ti] Título: Primary cutaneous anaplastic large-cell lymphoma: A case report. [So] Source: Medicine (Baltimore);97(4):e9645, 2018 Jan. [Is] ISSN: 1536-5964 [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: RATIONALE: Primary cutaneous anaplastic large-cell lymphoma (C-ALCL) is a rare cancer belonging to the group of primary T-cell lymphoproliferative diseases. C-ALCL is characterized by the presence of single or multiple ulcerated lesions on the skin's surface. PATIENT CONCERNS: This is the case of a 73-year-old man who reported to the Clinic of Cranio-Maxillofacial and Oral Surgery and Implantology, Medical University of Warsaw, owing to a skin tumor in the right parotideomasseteric region, initially diagnosed as discoid lupus erythematosus. During treatment for discoid lupus erythematosus, biopsy was repeated because of significant disease progression and dynamic tumor growth. Histopathological examination revealed the presence of pilomatrix carcinoma (trichilemmal carcinoma). Because of the discrepancy between clinical and histopathological findings, the tumor specimen was submitted to another facility, wherein lymphoma infiltration by anaplastic large cells was found in the dermis and subcutaneous tissue. DIAGNOSIS: C-ALCL. INTERVENTIONS: The patient was transferred to the Lymphoid Tumours Clinic of the Maria Sklodowska Curie Memorial Cancer Centre and Institute of Oncology in Warsaw, where chemotherapy was initiated. OUTCOMES: After 4 cycles of chemotherapy, a complete remission of skin lesions was achieved. During the 5-year follow-up, no recurrence occurred. LESSONS: C-ALCL is a rare type of cancer. Misdiagnosis can lead to inappropriate therapy and result in disease progression or unnecessary harm to the patient. [Mh] Termos MeSH primário: Erros de Diagnóstico Linfoma Anaplásico Cutâneo Primário de Células Grandes/diagnóstico Neoplasias Cutâneas/diagnóstico [Mh] Termos MeSH secundário: Idoso Diagnóstico Diferencial Doenças do Cabelo/diagnóstico Seres Humanos Lúpus Eritematoso Discoide/diagnóstico Masculino Pilomatrixoma/diagnóstico [Pt] Tipo de publicação: CASE REPORTS; JOURNAL ARTICLE [Em] Mês de entrada: 1802 [Cu] Atualização por classe: 180208 [Lr] Data última revisão: 180208 [Sb] Subgrupo de revista: AIM; IM [Da] Data de entrada para processamento: 180126 [St] Status: MEDLINE [do] DOI: 10.1097/MD.0000000000009645

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[PMID]: 28468609 [Au] Autor: Smaili W; Elalaoui SC; Meier S; Zerkaoui M; Sefiani A; Heinimann K [Ad] Endereço: Centre de Génomique Humaine - Faculté de Médecine et de Pharmacie, Université Mohamed V, Rabat, Morocco. [Ti] Título: A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case report. [So] Source: BMC Med Genet;18(1):50, 2017 05 03. [Is] ISSN: 1471-2350 [Cp] País de publicação: England [La] Idioma: eng [Ab] Resumo: BACKGROUND: Tricho-rhino-phalangeal syndrome (TRPS) is an autosomal dominant disorder characterized by craniofacial and skeletal malformations including short stature, thin scalp hair, sparse lateral eyebrows, pear-shaped nose and cone shaped epiphyses. This condition is caused by haploinsufficiency of the TRPS1 gene. Previous genotype-phenotype studies have correlated exon 6 missense mutations with TRPS type III, a severe form of type I with pronounced, facial characteristics, short stature and brachydactyly and differing from type II by the absence of exostoses and mental retardation. CASE PRESENTATION: We report the first case of a Moroccan family, a father and his three children, in which the diagnosis of type III TRPS was suspected based on severe clinical and radiological features. Molecular analysis of the TRPS1 gene revealed a novel missense mutation in exon 6, (p.Ala932Ser), located in the GATA-type DNA-binding zinc finger domain. CONCLUSION: Our observations in this kindred support the previous genotype-phenotype results suggesting that patients with more pronounced facial characteristics and more severe shortening of hands and feet are more likely to have mutation in exon 6 of TRPS1. [Mh] Termos MeSH primário: Proteínas de Ligação a DNA/genética Dedos/anormalidades Doenças do Cabelo/genética Síndrome de Langer-Giedion/genética Nariz/anormalidades Fatores de Transcrição/genética [Mh] Termos MeSH secundário: Adolescente Adulto Feminino Seres Humanos Masculino Marrocos Linhagem Adulto Jovem [Pt] Tipo de publicação: JOURNAL ARTICLE [Nm] Nome de substância: 0 (DNA-Binding Proteins); 0 (TRPS1 protein, human); 0 (Transcription Factors) [Em] Mês de entrada: 1706 [Cu] Atualização por classe: 171231 [Lr] Data última revisão: 171231 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 170505 [St] Status: MEDLINE [do] DOI: 10.1186/s12881-017-0413-8

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[PMID]: 28792655 [Au] Autor: Bendelsmith CR; Skrypek MM; Patel SR; Pond DA; Linabery AM; Bendel AE [Ad] Endereço: Department of Hematology-Oncology, Children's Minnesota, Minneapolis, Minnesota. [Ti] Título: Multiple pilomatrixomas in a survivor of WNT-activated medulloblastoma leading to the discovery of a germline APC mutation and the diagnosis of familial adenomatous polyposis. [So] Source: Pediatr Blood Cancer;65(1), 2018 Jan. [Is] ISSN: 1545-5017 [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: Because children diagnosed with WNT-activated medulloblastoma have a 10-year overall survival rate of 95%, active long-term follow-up is critically important in reducing mortality from other causes. Here, we describe an 11-year-old adopted female who developed multiple pilomatrixomas 3 years after diagnosis of WNT-activated medulloblastoma, an unusual finding that prompted deeper clinical investigation. A heterozygous germline APC gene mutation was discovered, consistent with familial adenomatous polyposis. Screening endoscopy revealed numerous precancerous polyps that were excised. This case highlights the importance of long-term follow-up of pediatric cancer survivors, including attention to unexpected symptoms, which might unveil an underlying cancer predisposition syndrome. [Mh] Termos MeSH primário: Proteína da Polipose Adenomatosa do Colo Polipose Adenomatosa do Colo Sobreviventes de Câncer Neoplasias Cerebelares Mutação em Linhagem Germinativa Doenças do Cabelo Meduloblastoma Segunda Neoplasia Primária Pilomatrixoma Neoplasias Cutâneas Proteínas Wnt [Mh] Termos MeSH secundário: Polipose Adenomatosa do Colo/diagnóstico Polipose Adenomatosa do Colo/genética Polipose Adenomatosa do Colo/metabolismo Polipose Adenomatosa do Colo/patologia Proteína da Polipose Adenomatosa do Colo/genética Proteína da Polipose Adenomatosa do Colo/metabolismo Neoplasias Cerebelares/diagnóstico Neoplasias Cerebelares/genética Neoplasias Cerebelares/metabolismo Neoplasias Cerebelares/patologia Criança Feminino Doenças do Cabelo/diagnóstico Doenças do Cabelo/genética Doenças do Cabelo/metabolismo Doenças do Cabelo/patologia Seres Humanos Meduloblastoma/diagnóstico Meduloblastoma/genética Meduloblastoma/metabolismo Meduloblastoma/patologia Segunda Neoplasia Primária/diagnóstico Segunda Neoplasia Primária/genética Segunda Neoplasia Primária/metabolismo Segunda Neoplasia Primária/patologia Pilomatrixoma/diagnóstico Pilomatrixoma/genética Pilomatrixoma/metabolismo Pilomatrixoma/patologia Neoplasias Cutâneas/diagnóstico Neoplasias Cutâneas/genética Neoplasias Cutâneas/metabolismo Neoplasias Cutâneas/patologia Proteínas Wnt/genética Proteínas Wnt/metabolismo [Pt] Tipo de publicação: CASE REPORTS; JOURNAL ARTICLE [Nm] Nome de substância: 0 (APC protein, human); 0 (Adenomatous Polyposis Coli Protein); 0 (Wnt Proteins) [Em] Mês de entrada: 1711 [Cu] Atualização por classe: 171129 [Lr] Data última revisão: 171129 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 170810 [St] Status: MEDLINE [do] DOI: 10.1002/pbc.26756

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[PMID]: 29064976 [Au] Autor: Awosika O; Burgess CM; Grimes PE [Ad] Endereço: *Department of Dermatology, The George Washington Medical Faculty Associates, Washington, DC; †Department of Dermatology, The George Washington University School of Medicine and Health Sciences, Washington, DC; ‡Department of Dermatology, Georgetown University School of Medicine, Washington, DC; §Division of Dermatology, University of California, Los Angeles, California. [Ti] Título: Considerations When Treating Cosmetic Concerns in Men of Color. [So] Source: Dermatol Surg;43 Suppl 2:S140-S150, 2017 Nov. [Is] ISSN: 1524-4725 [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: BACKGROUND: Men of color include a diverse population encompassing individuals with Fitzpatrick skin Types IV through VI. Yet, there is a paucity of data describing the cosmetic concerns of this population. OBJECTIVE: To review the basic science of advantages and disadvantages of skin of color and pathophysiology, incidence, and treatment of disorders of cosmetic concern in men of color. METHODS: A MEDLINE search was performed for publications on sex and racial differences in basic science of skin, common disorders in men of color, and evidence-based treatments. RESULTS: There are intrinsic differences in skin and hair of darker-complexioned men, particularly in Hispanics, African Americans, Asians, and Afro-Caribbeans. Advantages of darker skin include increased photoprotection, slowed aging, and a lower incidence of skin cancer. However, the increased content of melanin is associated with myriad dyschromias including melasma and postinflammatory hyperpigmentation (PIH). Additional common skin conditions of concern in men of color include pseudofolliculitis barbae, acne keloidalis nuchae, and keloids. CONCLUSION: A skin color conscious approach should be administered in caring for the cosmetic concerns of men of color that is cognizant of differences in biology of the skin and hair, associated PIH of disorders, and cultural/social practices among this population. [Mh] Termos MeSH primário: Grupos de Populações Continentais Técnicas Cosméticas Doenças do Cabelo/terapia Cabelo Dermatopatias/terapia Pigmentação da Pele [Mh] Termos MeSH secundário: Seres Humanos Masculino [Pt] Tipo de publicação: JOURNAL ARTICLE; REVIEW [Em] Mês de entrada: 1710 [Cu] Atualização por classe: 171103 [Lr] Data última revisão: 171103 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 171025 [St] Status: MEDLINE [do] DOI: 10.1097/DSS.0000000000001376

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[PMID]: 28954114 [Au] Autor: Shi G; Li W; Liang N; Wang TT; Zhou Y; Fan YM [Ad] Endereço: Department of Dermatology, Affiliated Hospital of Guangdong Medical University - Guangdong Province, China. [Ti] Título: Multiple vulvar dilated pores in a postmenopausal woman. [So] Source: An Bras Dermatol;92(4):562-564, 2017 Jul-Aug. [Is] ISSN: 1806-4841 [Cp] País de publicação: Brazil [La] Idioma: eng [Ab] Resumo: Winer's dilated pore is an infrequent appendageal tumor characterized by a giant comedone on the face, neck, and upper trunk in adults. We report a 57-year-old woman who developed multiple asymptomatic black papules on both labia majora. Histopathology showed grouped dilated follicles lined by keratinizing squamous epithelium in the superficial dermis. The superficial lining epithelium and interfollicular epidermis were atrophic, while the deep epithelium showed mild proliferation and melanin pigmentation with a few short projections extending into the surrounding dermis. We diagnosed multiple Winer's dilated pores based on late-onset lesions and pathological features. This patient may represent the first case of multiple vulvar Winer's dilated pores. We suggest that electrocautery may be effective for treating this type of superficial entity. [Mh] Termos MeSH primário: Folículo Piloso/patologia Nevo/patologia Neoplasias Cutâneas/diagnóstico Neoplasias Vulvares/diagnóstico [Mh] Termos MeSH secundário: Cistos/patologia Diagnóstico Diferencial Feminino Doenças do Cabelo/diagnóstico Seres Humanos Meia-Idade Pós-Menopausa Neoplasias Cutâneas/patologia Neoplasias Vulvares/patologia [Pt] Tipo de publicação: CASE REPORTS [Em] Mês de entrada: 1710 [Cu] Atualização por classe: 171010 [Lr] Data última revisão: 171010 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 170928 [St] Status: MEDLINE

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[PMID]: 28679382 [Au] Autor: Zaid AN; Jaradat NA; Eid AM; Al Zabadi H; Alkaiyat A; Darwish SA [Ad] Endereço: Department of Pharmacy, Faculty of Medicine and Health Sciences, An-Najah National University, P.O. Box 7, Nablus, Palestine. anzaid@najah.edu. [Ti] Título: Ethnopharmacological survey of home remedies used for treatment of hair and scalp and their methods of preparation in the West Bank-Palestine. [So] Source: BMC Complement Altern Med;17(1):355, 2017 Jul 05. [Is] ISSN: 1472-6882 [Cp] País de publicação: England [La] Idioma: eng [Ab] Resumo: BACKGROUND: Natural products have many uses and purposes, including those linked to pharmaceutics and cosmetics. The aim of this study was to investigate the use of natural remedies for the treatment of hair and scalp disorders in the West Bank, Palestine. METHODS: An ethnopharmacological survey of herbal remedies and other natural products used in cosmetics and cosmeceuticals was carried out in the West Bank, Palestine. A questionnaire was distributed to 267 herbalists, traditional healers, hairdressers and rural dwellers. Collected information included: the names of plants and other natural products, the parts used, hair conditions, diseases and problems for which these products were used and also their methods of preparation. To identify the most important species used, the factor of informant's consensus (F ), fidelity level (Fl) and the use-value (UV) were calculated. RESULTS: Collected data showed that 41 plants are utilized for the treatment of hair and scalp disorders, belonging to 27 families; among them Lamiaceae and Rosaceae, which were the most commonly used. Plant oils and their fruits are the most commonly used parts. Hair loss, dandruff, split hair endings and lice treatment, are reported as the most treated disorders. The number of plant species used consisted of 19, 14, 13, and again 13 with a factor of informant's consensus (Fic) for these disorders corresponding to 0.93, 0.94, 0.95 and 0.92, respectively. Fl was 100% for many plants; the highest UV value (0.84) was registered for Lawsonia inermis, which belongs to the Lythraceae family. CONCLUSIONS: This study showed that many natural remedies are still used in Palestine for the treatment of scalp and hair disorders as well as for cosmeceutical purposes. This study is of great importance as it allows us to have a greater perspective on our folkloric use of these natural products. A combined scientific effort between informants and the scientific community, working in this field, may help in the discovery of new cosmetics, cosmeceutical and nutraceutical products. [Mh] Termos MeSH primário: Etnofarmacologia Doenças do Cabelo/tratamento farmacológico Medicina Tradicional/utilização Preparações de Plantas/uso terapêutico Dermatoses do Couro Cabeludo/tratamento farmacológico [Mh] Termos MeSH secundário: Adolescente Adulto Composição de Medicamentos Feminino Cabelo/efeitos dos fármacos Doenças do Cabelo/etnologia Seres Humanos Masculino Meia-Idade Oriente Médio/etnologia Preparações de Plantas/química Dermatoses do Couro Cabeludo/etnologia Adulto Jovem [Pt] Tipo de publicação: JOURNAL ARTICLE [Nm] Nome de substância: 0 (Plant Preparations) [Em] Mês de entrada: 1708 [Cu] Atualização por classe: 170824 [Lr] Data última revisão: 170824 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 170707 [St] Status: MEDLINE [do] DOI: 10.1186/s12906-017-1858-1

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[PMID]: 28441830 [Au] Autor: Chen JJ; Shi LP [Ti] Título: [A case of tricho-hepato-enteric syndrome]. [So] Source: Zhonghua Er Ke Za Zhi;55(4):308-309, 2017 Apr 02. [Is] ISSN: 0578-1310 [Cp] País de publicação: China [La] Idioma: chi [Mh] Termos MeSH primário: Diarreia Infantil Facies Retardo do Crescimento Fetal Doenças do Cabelo [Mh] Termos MeSH secundário: Seres Humanos [Pt] Tipo de publicação: CASE REPORTS; JOURNAL ARTICLE [Em] Mês de entrada: 1708 [Cu] Atualização por classe: 170807 [Lr] Data última revisão: 170807 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 170427 [St] Status: MEDLINE [do] DOI: 10.3760/cma.j.issn.0578-1310.2017.04.015

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[PMID]: 28368926 [Au] Autor: Kyrpychova L; Carr RA; Martinek P; Vanecek T; Perret R; Chottová-Dvoráková M; Zamecnik M; Hadravsky L; Michal M; Kazakov DV [Ad] Endereço: *Sikl's Department of Pathology, Medical Faculty in Pilsen, Charles University in Prague, Pilsen, Czech Republic ‡Bioptical Laboratory ∥Biomedical Center, Faculty of Medicine in Pilsen and Charles University Medical Faculty Hospital, Pilsen ¶Agel Laboratory of Pathology, Novy Jicin, Czech Republic †Department of Histopathology, Warwick Hospital, Warwick, United Kingdom §Department of Pathology, University of Nantes, Nantes, France. [Ti] Título: Basal Cell Carcinoma With Matrical Differentiation: Clinicopathologic, Immunohistochemical, and Molecular Biological Study of 22 Cases. [So] Source: Am J Surg Pathol;41(6):738-749, 2017 Jun. [Is] ISSN: 1532-0979 [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: Basal cell carcinoma (BCC) with matrical differentiation is a fairly rare neoplasm, with about 30 cases documented mainly as isolated case reports. We studied a series of this neoplasm, including cases with an atypical matrical component, a hitherto unreported feature. Lesions coded as BCC with matrical differentiation were reviewed; 22 cases were included. Immunohistochemical studies were performed using antibodies against BerEp4, ß-catenin, and epithelial membrane antigen (EMA). Molecular genetic studies using Ion AmpliSeq Cancer Hotspot Panel v2 by massively parallel sequencing on Ion Torrent PGM were performed in 2 cases with an atypical matrical component (1 was previously subjected to microdissection to sample the matrical and BCC areas separately). There were 13 male and 9 female patients, ranging in age from 41 to 89 years. Microscopically, all lesions manifested at least 2 components, a BCC area (follicular germinative differentiation) and areas with matrical differentiation. A BCC component dominated in 14 cases, whereas a matrical component dominated in 4 cases. Matrical differentiation was recognized as matrical/supramatrical cells (n=21), shadow cells (n=21), bright red trichohyaline granules (n=18), and blue-gray corneocytes (n=18). In 2 cases, matrical areas manifested cytologic atypia, and a third case exhibited an infiltrative growth pattern, with the tumor metastasizing to a lymph node. BerEP4 labeled the follicular germinative cells, whereas it was markedly reduced or negative in matrical areas. The reverse pattern was seen with ß-catenin. EMA was negative in BCC areas but stained a proportion of matrical/supramatrical cells. Genetic studies revealed mutations of the following genes: CTNNB1, KIT, CDKN2A, TP53, SMAD4, ERBB4, and PTCH1, with some differences between the matrical and BCC components. It is concluded that matrical differentiation in BCC in most cases occurs as multiple foci. Rare neoplasms manifest atypia in the matrical areas. Immunohistochemical analysis for BerEP4, EMA, and ß-catenin can be helpful in limited biopsy specimens. From a molecular biological prospective, BCC and matrical components appear to share some of the gene mutations but have differences in others, but this observation must be validated in a large series. [Mh] Termos MeSH primário: Carcinoma Basocelular/patologia Doenças do Cabelo/patologia Pilomatrixoma/patologia Neoplasias Cutâneas/patologia [Mh] Termos MeSH secundário: Adulto Idoso Idoso de 80 Anos ou mais Biomarcadores Tumorais/genética Biomarcadores Tumorais/metabolismo Carcinoma Basocelular/genética Carcinoma Basocelular/metabolismo Carcinoma Basocelular/mortalidade Diferenciação Celular Feminino Seguimentos Doenças do Cabelo/genética Doenças do Cabelo/metabolismo Doenças do Cabelo/mortalidade Sequenciamento de Nucleotídeos em Larga Escala Seres Humanos Imuno-Histoquímica Masculino Meia-Idade Mutação Pilomatrixoma/genética Pilomatrixoma/metabolismo Pilomatrixoma/mortalidade Prognóstico Neoplasias Cutâneas/genética Neoplasias Cutâneas/metabolismo Neoplasias Cutâneas/mortalidade [Pt] Tipo de publicação: JOURNAL ARTICLE [Nm] Nome de substância: 0 (Biomarkers, Tumor) [Em] Mês de entrada: 1709 [Cu] Atualização por classe: 170901 [Lr] Data última revisão: 170901 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 170404 [St] Status: MEDLINE [do] DOI: 10.1097/PAS.0000000000000841

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[PMID]: 28329524 [Au] Autor: Vázquez-Osorio I; García SM; Rodríguez-Díaz E; Gonzalvo-Rodríguez P [Ad] Endereço: Hospital Universitario de Cabueñes, Servicio de Dermatología, Gijón, Asturias, España. rogivaos@gmail.com. [Ti] Título: Anetodermic pilomatricoma: clinical, histopathologic, and sonographic findings. [So] Source: Dermatol Online J;23(3), 2017 Mar 15. [Is] ISSN: 1087-2108 [Cp] País de publicação: United States [La] Idioma: eng [Ab] Resumo: Pilomatricoma is a benign cutaneous tumor originatingfrom hair matrix cells. Anetodermic changes inthe skin overlying pilomatricomas are sometimesreported, although their precise mechanisms remainunknown. We present an unusual case of anetodermicpilomatricoma on the upper extremity of a 17-yearoldboy and report its clinical, histopathologic, andsonographic findings. [Mh] Termos MeSH primário: Anetodermia/diagnóstico Calcinose/diagnóstico Doenças do Cabelo/diagnóstico Pilomatrixoma/diagnóstico Neoplasias Cutâneas/diagnóstico [Mh] Termos MeSH secundário: Adolescente Anetodermia/diagnóstico por imagem Anetodermia/patologia Anetodermia/cirurgia Braço Calcinose/diagnóstico por imagem Calcinose/patologia Calcinose/cirurgia Doenças do Cabelo/diagnóstico por imagem Doenças do Cabelo/patologia Doenças do Cabelo/cirurgia Seres Humanos Masculino Pilomatrixoma/diagnóstico por imagem Pilomatrixoma/patologia Pilomatrixoma/cirurgia Neoplasias Cutâneas/diagnóstico por imagem Neoplasias Cutâneas/patologia Neoplasias Cutâneas/cirurgia Ultrassonografia [Pt] Tipo de publicação: CASE REPORTS; JOURNAL ARTICLE [Em] Mês de entrada: 1710 [Cu] Atualização por classe: 171017 [Lr] Data última revisão: 171017 [Sb] Subgrupo de revista: IM [Da] Data de entrada para processamento: 170323 [St] Status: MEDLINE

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