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Korean Journal of Pathology ; : 93-99, 2013.
Artigo em Inglês | WPRIM | ID: wpr-56555

RESUMO

Acinar cell carcinoma is a rare malignant epithelial neoplasm with predominantly exocrine acinar differentiation and is seen primarily in older men (mean age, 62 years). The presenting symptoms are usually non-specific, and jaundice is often not present. Symptoms relating to the overproduction and release of lipase into the circulation are present in 10-15% of patients. Characteristic cytomorphologic features include a population of cells with minimal pleomorphism, eccentrically placed nuclei with a single prominent nucleoli and moderate hyperchromasia. The cytoplasm is finely granular, and the background may contain granular debris secondary to cytolysis. A significant proportion of the cases also have a minor neuroendocrine component or scattered neuroendocrine cells. Approximately 50% of patients have metastatic disease at presentation, often restricted to the regional lymph nodes and liver. The prognosis is poor, only slightly better than that of pancreatic ductal adenocarcinoma.


Assuntos
Humanos , Masculino , Células Acinares , Adenocarcinoma , Carcinoma , Carcinoma de Células Acinares , Citoplasma , Icterícia , Lipase , Fígado , Linfonodos , Células Neuroendócrinas , Pâncreas , Ductos Pancreáticos , Prognóstico
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