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1.
J BUON ; 19(1): 221-7, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24659668

RESUMEN

PURPOSE: The canonical signaling pathway for the transforming growth factor-beta (TGF-ß) family is through the Smad proteins which are pivotal intracellular mediators of TGF-ß family members. Recently, disruption of the TGF-ß pathway in cancer has been demonstrated at the level of the Smad signal transducers. In this study, we examined Smad4 and Smad7 expression in gastric carcinomas to elucidate their role in tumor progression. METHODS: The immunohistochemical expression of Smad4 and Smad7 was evaluated in 151 surgically resected samples of gastric adenocarcinoma in order to examine their correlation with clinicopathologic findings and patients' survival. RESULTS: Smad4 and Smad7 expression (low, moderate or strong) was observed in 86.7% (131/151) and 33.1% (50/151) of gastric adenocarcinoma tumor samples, respectively. Our results revealed that the loss of Smad4 expression correlated significantly with the intestinal type, male sex, depth of tumor and poor survival. Smad7 expression was significantly more frequent in intestinal type and well differentiated gastric adenocarcinomas and significantly correlated with the duration of disease-free survival. CONCLUSION: Smad signal transducers are considered as important molecules in tumor development and progression and the evaluation of their expression in human gastric cancer could be useful in selecting stage I patients who should be considered as candidates for adjuvant chemotherapy.


Asunto(s)
Adenocarcinoma/genética , Proteína Smad4/biosíntesis , Proteína smad7/biosíntesis , Neoplasias Gástricas/genética , Adenocarcinoma/patología , Adulto , Anciano , Anciano de 80 o más Años , Diferenciación Celular/genética , Supervivencia sin Enfermedad , Femenino , Regulación Neoplásica de la Expresión Génica , Humanos , Masculino , Persona de Mediana Edad , Transducción de Señal , Proteína Smad4/genética , Proteína smad7/genética , Neoplasias Gástricas/patología
2.
J BUON ; 19(3): 605-17, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25261642

RESUMEN

A considerable change in the anatomical distribution of colorectal cancer (CRC) towards more proximal sites has been observed in Western countries within the last 6-7 decades. As a result, tumors located proximally to the splenic flexure are now accounting for 30-40% (or even more) of overall CRC cases. This proximal migration is not always representing a true increase of proximal cancer, arising from various combinations of changes in the rates of proximal and distal cancer (e.g. proximal increase with distal stability/reduction, or decline in both sites albeit higher distally etc) in different areas and periods. Principal potential causes include ageing in Western populations (since proximal cancers are more common among the aged), various potentially site-specific exposures (lifestyle and medical) and systematic screening. Their effect is reflected in the particular shift patterns; for instance, widespread screening in USA has led to an overall CRC decline, more evident distally (for technical, anatomical and morphological reasons). Segmental disparities in particular characteristics (age, gender, morphology) and responses to various exposures are etiologically associated (for the most part) with underlying genetic differences between proximal and distal tumors. From clinical aspect, proximal shift necessitates a more generalized use of colonoscopy in screening programs. Potential interventions in treatment (segmental patient stratification) and prevention (identification of particular site-specific exposures) require further investigation.


Asunto(s)
Neoplasias Colorrectales/etiología , Factores de Edad , Neoplasias Colorrectales/epidemiología , Detección Precoz del Cáncer , Predisposición Genética a la Enfermedad , Humanos , Estilo de Vida , Estadificación de Neoplasias , Factores Sexuales
3.
Urology ; 83(6): 1409-11, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24767825

RESUMEN

Pseudosarcomatous myofibroblastic proliferations are very unusual entities of unknown etiology. Despite its benign nature, this entity can easily be misdiagnosed (both clinically and histologically) as a malignant neoplasm. Hereby, we report a case of a 15-year-old woman who presented to our hospital with a broad-based polypoid mass located in the left posterior wall of the urinary bladder. The patient underwent a transurethral resection of the lesion. Morphologic and immunohistochemical findings suggested the diagnosis of pseudosarcomatous myofibroblastic proliferation. The patient is free of recurrence 5 years after surgery.


Asunto(s)
Transformación Celular Neoplásica/patología , Miofibroblastos/patología , Pólipos/patología , Sarcoma/patología , Neoplasias de la Vejiga Urinaria/patología , Adolescente , Biopsia con Aguja , Proliferación Celular , Diagnóstico Diferencial , Femenino , Estudios de Seguimiento , Hematuria/diagnóstico , Hematuria/etiología , Humanos , Inmunohistoquímica , Miofibroblastos/citología , Pólipos/complicaciones , Pólipos/diagnóstico , Pólipos/cirugía , Enfermedades Raras , Medición de Riesgo , Resultado del Tratamiento , Enfermedades de la Vejiga Urinaria/complicaciones , Enfermedades de la Vejiga Urinaria/diagnóstico , Enfermedades de la Vejiga Urinaria/patología , Enfermedades de la Vejiga Urinaria/cirugía , Neoplasias de la Vejiga Urinaria/complicaciones , Neoplasias de la Vejiga Urinaria/diagnóstico , Neoplasias de la Vejiga Urinaria/cirugía
4.
Case Rep Oncol Med ; 2014: 305848, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25197591

RESUMEN

Gastrointestinal stromal tumors (GISTs) represent the majority of primary mesenchymal tumors of the gastrointestinal tract. They are generally considered to be solitary tumors and therefore the synchronous occurrence with other primary malignancies of gastrointestinal track is considered a rare event. Here we present the case of a 75-year-old man admitted to our hospital with a 10-day history of gastrointestinal bleeding. Colonoscopy revealed an ulcerative mass of 4 cm in diameter in the ascending colon. Gastroscopy revealed a bulge in the gastric body measuring 1 cm in diameter with normal overlying mucosa. Surgical intervention was suggested and ileohemicolectomy with regional lymph node resection along with gastric wedge resection was performed. Pathologic examination of the ascending colon mass showed an invasive moderately differentiated adenocarcinoma stage III B (T3N1M0). Grossly resected wedge of stomach showed a well circumscribed intramural tumor which microscopically was consistent with essentially benign gastrointestinal stromal tumor (according to Miettinen criteria). The patient did not receive additional treatment. Two years later the patient showed no evidence of recurrence or metastasis.

5.
Case Rep Oncol ; 4(1): 132-5, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21691571

RESUMEN

Leydig cell tumour is a benign testicular non-germ cell tumour, and malignant transformation is rare. We report a case of a 35-year-old man who came to our hospital with a painless left testicular mass measuring 1.2 × 1 cm. Histological evaluation of the tumour showed features of a malignant Leydig cell tumour but no infiltration beyond the capsule or metastasis. The small size of the tumour was remarkable.

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