ABSTRACT
Objective: This study was aimed at evaluating the usefulness of paired box-2 gene (PAX-2) in the diagnosis of renal tumors. Materials and Methods: This study included 60 renal tumors. The newly prepared hematoxylin and eosin stained slides of all cases were evaluated and the diagnoses were confirmed or revised for each tumor according to the 2004 World Health Organization classification of renal tumors. Representative and consecutive sections of each tumor were submitted for anti-PAX-2 antibody immunohistochemistry. The pattern of staining (nuclear or cytoplasmic) was also noted. PAX-2 expression in tumors was correlated with low- and high-nuclear grades (Fuhrman nuclear grades). Results: The 45/60 (75%) cases showed PAX-2 nuclear immunoexpression. The frequency of positivity in renal tumors was seen in 29/34 (85.5%) and 12/15 (80%) cases of clear cell RC, papillary RCC, respectively. The PAX-2 was positive in 20/45 cases for score 1+. The 16/45 cases were categorized into score 2+, and 9/45 cases were categorized into score 3+. Conclusion: PAX-2 is a diagnostically useful marker for primary renal tumors and is inversely proportion to the grades of the renal tumor.
ABSTRACT
Fundamento: La atrofia multisistémica es un trastorno neurodegenerativo esporádico, que puede comenzar alrededor de los 60 años y ocasiona invalidez progresiva hasta la dependencia total de un cuidador. Presentación de caso: Se presenta el caso de un hombre de 57 años de edad que comenzó con cuadros de inestabilidad para la marcha y torpeza para realizar las actividades cotidianas y se interpretó como una enfermedad de Parkinson con pobre respuesta a la levodopa con bencerazida. Durante su estudio agravó los síntomas neurológicos y al realizar una tomografía axial computarizada de cráneo se evidenció atrofia cerebelosa y frontal que apoyó el diagnóstico de una atrofia multisistémica tipo C. Recibió tratamiento con levodopa con bencerazida, amantadina, y hubo alivio sintomático de la hipotensión ortostática. Conclusiones: El diagnóstico precoz de la enfermedad se dificultó por su comienzo similar a otras enfermedades neurodegenerativas, y su evolución ocasionó pérdida progresiva del validismo del paciente, sin que el tratamiento modificara el curso de la misma.
Background: The multiple system atrophy is a sporadic neurodegenerative disorder that may begin around age 60 and causes progressive disability to total dependence on a caregiver. Case report: A case presentation of a 57 year-old man who started with signs of unsteady gait and clumsiness in performing daily activities and which was interpreted as Parkinson's disease with poor response to levodopa with benserazide. During his study the patient showed worsening neurological symptoms and a computerized tomography of the skull was performed corroborating head and front cerebellar atrophy which supported the diagnosis of multiple system atrophy type C. He received treatment with levodopa together benserazide, and amantadine and a symptomatic relief of orthostatic hypotension was observed. Conclusions: Early diagnosis of the disease was hindered by its similar onset to other neurodegenerative diseases and its evolution caused progressive loss of the patient´s walking ability and the treatment did not modify the course of the disease.