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1.
J Dtsch Dermatol Ges ; 17(8): 800-808, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31437373

RESUMEN

BACKGROUND AND OBJECTIVES: Overall survival (OS) in patients with early-stage malignant melanoma differs. To date, there are no established prognostic markers. We aimed to contribute to a better understanding of potential prognostic immunohistochemical markers for risk stratification. PATIENTS AND METHODS: 161 surgically resected early-stage malignant melanomas (stage pT1 and pT2) were analyzed for expression of 20 different proteins using immunohistochemistry. The results were correlated with OS. The cohort was randomly split into a discovery and a validation cohort. RESULTS: High Bcl-2 expression, high nuclear S100A4 expression as well as a Ki67 proliferation index of ≥ 20 % were associated with shorter OS. Strong MITF immunoreactivity was a predictor for favorable prognosis. A combination of these four markers resulted in a multi-marker score with significant prognostic value in multivariate survival analysis (HR: 3.704; 95 % CI 1.484 to 9.246; p = 0.005). Furthermore, the score was able to differentiate a low-risk group with excellent OS rates (five-year survival rate: 100 %), an intermediate-risk group (five-year survival rate: 81.8 %) and a high-risk group (five-year survival rate: 52.6 %). The prognostic value was confirmed within the validation cohort. CONCLUSIONS: Combined immunohistochemical analysis of Bcl-2, nuclear S100A4, Ki67 and MITF could contribute to better risk stratification of early-stage malignant melanoma patients.


Asunto(s)
Biomarcadores de Tumor/metabolismo , Inmunohistoquímica/métodos , Melanoma/metabolismo , Neoplasias Cutáneas/metabolismo , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Antígeno Ki-67/metabolismo , Masculino , Melanoma/mortalidad , Melanoma/patología , Factor de Transcripción Asociado a Microftalmía/metabolismo , Persona de Mediana Edad , Índice Mitótico , Estadificación de Neoplasias , Pronóstico , Proteínas Proto-Oncogénicas c-bcl-2/metabolismo , Medición de Riesgo , Factores de Riesgo , Proteína de Unión al Calcio S100A4/metabolismo , Neoplasias Cutáneas/mortalidad , Neoplasias Cutáneas/patología
3.
Dtsch Med Wochenschr ; 143(23): 1682-1689, 2018 11.
Artículo en Alemán | MEDLINE | ID: mdl-30440072

RESUMEN

Evaluation of skin diseases can be challenging for non-dermatologists. Even obvious well-characterized skin pathologies might be misleading and thus treatment can fail. Particularly the differentiation of surgical treated entities is important, for example the management of a wound healing disturbance profoundly differs from that of a pyoderma gangrenosum. This article outlines several easily mistaken pairs of dermatologic entities on one hand and surgical on the other. For example, a livedo vasculopathy can be confused with a leg ulcer, a nail melanoma with a simple hematoma and finally a hidradenitis suppurativa with an axillary abscess. Typical clinical signs and anamnestic data may often lead to the right diagnosis also assisted by the simple fact to "keep it in mind".


Asunto(s)
Procedimientos Quirúrgicos Dermatologicos , Enfermedades de la Piel , Diagnóstico Diferencial , Humanos , Enfermedades de la Piel/diagnóstico , Enfermedades de la Piel/cirugía
4.
Head Neck ; 37(6): 829-34, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24946737

RESUMEN

BACKGROUND: Atypical fibroxanthoma is a rare mesenchymal tumor of the head and neck region. METHODS: We analyzed the files of 3 large dermatology hospitals from the years 2001 to 2013 in southeast Germany. RESULTS: We identified 53 patients (56 tumors) with a male predominance. The mean age was 78.0 years ± 8.3 years. Mohs surgery was performed in all cases resulting in complete remission in 45 patients. Five patients had a relapse within 2 years, and 4 developed metastases. None of the tumors with a safety margin of ≥2 cm relapsed. The majority of cases were found in the Dresden region. CONCLUSION: Atypical fibroxanthoma demonstrates an uneven geographic distribution in southeast Germany that demands further investigations. Mohs surgery with ≥2 cm safety margins is the treatment of choice. A regular follow-up is recommended.


Asunto(s)
Histiocitoma Fibroso Benigno/epidemiología , Histiocitoma Fibroso Benigno/patología , Recurrencia Local de Neoplasia/epidemiología , Neoplasias Cutáneas/epidemiología , Neoplasias Cutáneas/patología , Anciano , Anciano de 80 o más Años , Biopsia con Aguja , Bases de Datos Factuales , Supervivencia sin Enfermedad , Femenino , Estudios de Seguimiento , Alemania/epidemiología , Histiocitoma Fibroso Benigno/cirugía , Humanos , Inmunohistoquímica , Masculino , Persona de Mediana Edad , Cirugía de Mohs/métodos , Recurrencia Local de Neoplasia/patología , Recurrencia Local de Neoplasia/terapia , Estudios Retrospectivos , Medición de Riesgo , Neoplasias Cutáneas/cirugía , Análisis de Supervivencia , Resultado del Tratamiento
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