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Acinar cell carcinoma of the pancreas

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Pancreatic acinar cell carcinoma is a rare neoplasm (comprising about 1% of pancreatic tumours). We studied three cases (61‐year‐old female; 42‐year‐old male; 57‐year‐old male), whose survival after diagnosis ranged from 1 year 2 months to 6 years 8 months. There were widespread metastases in each case. The tumours had acinar, trabecular and solid growth patterns. By immunohistochemistry, pancreatic acinar cell markers including carboxyl ester lipase, pancreatic secretory trypsin inhibitor and pancreatic phospholipase A2 (group I PLA2) gave a strong positive reaction in all three cases. By electron microscopy, zymogen granules were seen in the cytoplasm of the tumour cells. Immunostaining for prostate‐specific antigen was positive in all three cases. Above‐normal concentrations of pancreatic PLA2 were measured in the serum of one patient and the values decreased during chemotherapy concomitantly with the reduction in the size of the tumour mass. In conclusion, immunohisto‐chemical demonstration of the secretory products of acinar cells including the new marker pancreatic PLA2 is useful in the differential diagnosis of pancreatic acinar cell carcinoma. Determination of the concentration of pancreatic group I PLA2 in serum may be helpful in the evaluation of therapy.
Title: Acinar cell carcinoma of the pancreas
Description:
Pancreatic acinar cell carcinoma is a rare neoplasm (comprising about 1% of pancreatic tumours).
We studied three cases (61‐year‐old female; 42‐year‐old male; 57‐year‐old male), whose survival after diagnosis ranged from 1 year 2 months to 6 years 8 months.
There were widespread metastases in each case.
The tumours had acinar, trabecular and solid growth patterns.
By immunohistochemistry, pancreatic acinar cell markers including carboxyl ester lipase, pancreatic secretory trypsin inhibitor and pancreatic phospholipase A2 (group I PLA2) gave a strong positive reaction in all three cases.
By electron microscopy, zymogen granules were seen in the cytoplasm of the tumour cells.
Immunostaining for prostate‐specific antigen was positive in all three cases.
Above‐normal concentrations of pancreatic PLA2 were measured in the serum of one patient and the values decreased during chemotherapy concomitantly with the reduction in the size of the tumour mass.
In conclusion, immunohisto‐chemical demonstration of the secretory products of acinar cells including the new marker pancreatic PLA2 is useful in the differential diagnosis of pancreatic acinar cell carcinoma.
Determination of the concentration of pancreatic group I PLA2 in serum may be helpful in the evaluation of therapy.

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