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1.
Rev Esp Enferm Dig ; 89(4): 317-9, 1997 Apr.
Article Es | MEDLINE | ID: mdl-9221021

Neuroendocrine cells are frequently found in gastric tumours, although they rarely make up more than one third of the total number of tumour cells. When juxtapositioning of the two kinds of tumour cells occurs a "collision tumour" is formed. These have been described to occur with varying frequency throughout the digestive tract. They are uncommon in the stomach. We describe a case, of a gastric collision tumour in which an adenocarcinoma coexisted with a carcinoide tumour and there were zones of bony metaplasia in the transition area between the two tumors. Positive CEA, VIP, beta-HCG and TSH on inmunohistochemical analysis was found.


Adenocarcinoma/pathology , Carcinoid Tumor/pathology , Stomach Neoplasms/pathology , Aged , Humans , Male , Metaplasia
2.
Rev Esp Enferm Dig ; 88(10): 672-6, 1996 Oct.
Article Es | MEDLINE | ID: mdl-8983306

We describe ten cases of ectopic pancreas operated on in the Hospital General Universitario, Alicante, between 1970 and 1994. Average age of patients was 47.7 (range 3-75); five men and five women. In four cases there was associated digestive tract bleeding, three had chronic gastroduodenal ulcers, two pancreaticobiliary disease, and one suprarenal abnormalities. In four cases the ectopic gland was found in the gastric antrum; in four cases in the duodenum and in the remaining two cases in the first jejunal loop. Average diameter was 2.3 cm (range 0.6-6). In six cases complete pancreas tissue was found, in three an exocrine pancreas and in one a purely endocrine pancreas. In two patients the presence of the choristoma and the clinical findings due to erosion of the subjacent mucosa may be related. In one case the finding of cholelithiasis, intradiverticular papilla, and periampullar ectopia together with clinical features of recurrent pancreatitis may also be linked. In the remaining seven cases no relationship was found between the ectopic pancreas and the clinical features. Our series suggest that simple resection is best to avoid complications.


Choristoma/pathology , Duodenal Diseases/pathology , Jejunal Diseases/pathology , Pancreas , Stomach Diseases/pathology , Adult , Aged , Child, Preschool , Female , Humans , Male , Middle Aged
3.
Rev Esp Enferm Dig ; 85(3): 217-9, 1994 Mar.
Article Es | MEDLINE | ID: mdl-8204388

We report a case of granular cell tumor of the cystic duct. We have found only 47 such tumors of the biliary tract reported in the literature. Main symptoms at presentation are abdominal pain or obstructive jaundice. The clinical diagnosis is often difficult and the differential diagnosis is established with other more frequent conditions, including malignant neoplasms. Surgical excision is curative.


Bile Duct Neoplasms/pathology , Cystic Duct , Granular Cell Tumor/pathology , Adult , Humans , Male
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