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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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