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1.
Pathol Oncol Res ; 22(3): 515-21, 2016 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-26683836

RESUMEN

The purpose of this study was to investigate the role of E-cadherin, p53, and inhibin-α immunostaining in the differential diagnosis of hydropic abortion (HA), partial hydatidiform mole (PHM), and complete hydatidiform mole (CHM). E-cadherin, p53, and inhibin-α protein expression patterns were investigated immunohistochemically using paraffin -embedded tissue sections from histologically diagnosed cases of HA (n = 23), PHM (n = 24), and CHM (n = 23). Expression patterns of these markers were scored semi-quantitatively according to the staining intensity, percentage of positive cells, and immunoreactivity score. Classification of cases was established on histologic criteria and supported by the molecular genotyping. Immunostaining allowed the identification of specific cell types with E-cadherin, p53, and inhibin-α expression in all cases. E-cadherin expression was detected on the cell surface of villous cytotrophoblasts. We observed a marked decline in the expression of E-cadherin from HAs to PHMs to CHMs. The p53-positive reaction was restricted to the nucleus of villous cytotrophoblasts. Significantly increased p53 expression was observed in CHMs, compared with HAs and PHMs. The expression of inhibin-α was localised in the cytoplasm of villous syncytiotrophoblasts, and the expression of this marker was significantly higher in PHMs and CHMs than HAs. In conclusion, immunohistochemical analysis of E-cadherin, p53, and inhibin-α expression could serve as a useful adjunct to conventional methods in the differential diagnosis of HA, PHM, and CHM.


Asunto(s)
Aborto Espontáneo/metabolismo , Cadherinas/metabolismo , Mola Hidatiforme/metabolismo , Inhibinas/metabolismo , Proteína p53 Supresora de Tumor/metabolismo , Neoplasias Uterinas/metabolismo , Adolescente , Adulto , Antígenos CD , Biomarcadores/metabolismo , Diagnóstico Diferencial , Femenino , Humanos , Inmunohistoquímica/métodos , Persona de Mediana Edad , Embarazo , Trofoblastos/metabolismo , Adulto Joven
2.
Arq Bras Oftalmol ; 78(5): 323-5, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26466235

RESUMEN

Primary cutaneous adenoid cystic carcinoma (PCACC) is a rare malignant epithelial tumor most commonly observed in the scalp and skin of the chest and originating from the palpebral portion of the lacrimal gland in the orbit. Here we describe the diagnosis and treatment of a rare case of PCACC in an eye of a 52-year-old male. The patient presented with a mass lesion of the right lower eyelid. During incisional biopsy, lack of encapsulation and a secretion pattern different to that of chalazion was observed, which differentiated the lesion from chalazion. Pathological analysis revealed the diagnosis of PCACC. This case highlights the importance of careful inspection for macroscopic differentiation of PCACC from chalazion after initial surgery and pathological evaluation of all surgically removed mass lesions for accurate diagnosis and treatment.


Asunto(s)
Carcinoma Adenoide Quístico/patología , Neoplasias de los Párpados/patología , Neoplasias Cutáneas/patología , Biopsia , Carcinoma Adenoide Quístico/cirugía , Chalazión/patología , Neoplasias de los Párpados/cirugía , Humanos , Masculino , Persona de Mediana Edad , Neoplasias Cutáneas/cirugía
3.
Arq. bras. oftalmol ; 78(5): 323-325, Sep.-Oct. 2015. ilus
Artículo en Inglés | LILACS | ID: lil-761529

RESUMEN

ABSTRACTPrimary cutaneous adenoid cystic carcinoma (PCACC) is a rare malignant epithelial tumor most commonly observed in the scalp and skin of the chest and originating from the palpebral portion of the lacrimal gland in the orbit. Here we describe the diagnosis and treatment of a rare case of PCACC in an eye of a 52-year-old male. The patient presented with a mass lesion of the right lower eyelid. During incisional biopsy, lack of encapsulation and a secretion pattern different to that of chalazion was observed, which differentiated the lesion from chalazion. Pathological analysis revealed the diagnosis of PCACC. This case highlights the importance of careful inspection for macroscopic differentiation of PCACC from chalazion after initial surgery and pathological evaluation of all surgically removed mass lesions for accurate diagnosis and treatment.


RESUMOO carcinoma adenóide cístico cutâneo primário (PCACC) é um tumor maligno epitelial raro, mais comumente observado no couro cabeludo e na pele do peito sendo originário da porção palpebral da glândula lacrimal na órbita. Apresentamos o diagnóstico e tratamento de um caso raro de carcinoma adenóide cístico cutâneo primário do olho em um paciente do sexo masculino de 52 anos de idade, com uma lesão maciça da pálpebra inferior direita. A observação da falta de encapsulamento e um padrão de secreção diferente do calázio durante biópsia incisional permitiu a diferenciação da lesão de um calázio. A avaliação dos resultados do exame patológico resultou no diagnóstico de carcinoma adenóide cístico cutâneo primário. A análise do caso indica a importância de uma inspeção cuidadosa para a diferenciação macroscópica da carcinoma adenóide cístico cutâneo primário do calázio após a cirurgia inicial e avaliação patológica de todas as lesões de massa removidas cirurgicamente para o diagnóstico e tratamento corretos.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Carcinoma Adenoide Quístico/patología , Neoplasias de los Párpados/patología , Neoplasias Cutáneas/patología , Biopsia , Carcinoma Adenoide Quístico/cirugía , Chalazión/patología , Neoplasias de los Párpados/cirugía , Neoplasias Cutáneas/cirugía
4.
Asian Pac J Cancer Prev ; 16(3): 1041-5, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25735328

RESUMEN

BACKGROUND: Paget's disease (PD) is a rare form of intraepithelial adenocarcinoma that involves breast and extramammarian tissues. It is often associated with ductal carcinoma in situ and/or invasive ductal cancer. Molecular pathways that play a role in development of Paget's disease are stil unclear. Expression patterns of Cox-2 and bcl-2 were therefore assessed. MATERIALS AND METHODS: Patients with a histopathological diagnosis of Paget's disease were included in this study. Patient files were analysed retrospectively. RESULTS: Invasive cancer was diagnosed in 35 (76.1%) of the patients, 7 (15.2%) had ductal carcinoma in situ and 4 (8.7%) patients had no associated neoplasm. Twenty four (52.2%) patients showed COX-2 expression in Paget cells whereas no expression was seen in 22 (47.8%) patients. No relation was found between COX-2 expression and the lesion underlying Paget's disease (p=0.518). Bcl-2 expression in Paget cells was found positive in 12 (26.1%) and negative in 27 (58,7%) cases. There was no relation between Bcl-2 expression and the lesion accompanying Paget's disease (p=0.412). No relation was observed between COX-2 expression and Bcl-2 expression (p=0.389). CONCLUSIONS: In breast cancer, COX-2 expression is associated with poor prognostic factors. As COX-2 expression increases the tendency to metastasize also increases. In our study we found a significantly high COX-2 expression in Paget's disease of the breast. We suggest that COX-2 expression and inflammatory processes may play a role in pathogenesis of the Paget's disease of the breast.


Asunto(s)
Adenocarcinoma/metabolismo , Biomarcadores de Tumor/metabolismo , Neoplasias de la Mama/metabolismo , Carcinoma Ductal de Mama/metabolismo , Carcinoma Intraductal no Infiltrante/metabolismo , Ciclooxigenasa 2/metabolismo , Enfermedad de Paget Mamaria/metabolismo , Proteínas Proto-Oncogénicas c-bcl-2/metabolismo , Adenocarcinoma/patología , Adulto , Anciano , Anciano de 80 o más Años , Neoplasias de la Mama/patología , Carcinoma Ductal de Mama/patología , Carcinoma Intraductal no Infiltrante/patología , Femenino , Estudios de Seguimiento , Humanos , Técnicas para Inmunoenzimas , Persona de Mediana Edad , Estadificación de Neoplasias , Enfermedad de Paget Mamaria/patología , Pronóstico , Estudios Retrospectivos , Adulto Joven
5.
BMJ Case Rep ; 20142014 Jun 25.
Artículo en Inglés | MEDLINE | ID: mdl-24966256

RESUMEN

A 40-year-old man presented to us with infertility. During scrotal ultrasonography, a heterogeneous nodular mass was seen in the right testicle. Surprisingly, histopathological examination revealed shadow cells, which are the characteristic feature of pilomatrixomas.


Asunto(s)
Infertilidad Masculina/diagnóstico por imagen , Pilomatrixoma/patología , Escroto/diagnóstico por imagen , Neoplasias Testiculares/diagnóstico , Testículo/patología , Adulto , Humanos , Masculino , Pilomatrixoma/diagnóstico por imagen , Neoplasias Testiculares/diagnóstico por imagen , Testículo/diagnóstico por imagen , Ultrasonografía
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