A Case of Paraduodenal Pancreatitis and Immunohistochemical Analysis
±Ç¹ÌÁ¤, ³²Àº¼÷, Á¶¼ºÁø, ½ÅÇü½Ä, ±èÁÖ¼·, ±èµÎÁø,
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±Ç¹ÌÁ¤ ( Kwon Mi-Jung )
¼º±Õ°ü´ëÇб³ ÀÇ°ú´ëÇÐ »ï¼º¼¿ïº´¿ø º´¸®Çб³½Ç
³²Àº¼÷ ( Nam Eun-Sook )
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ °µ¿¼º½Éº´¿ø º´¸®Çб³½Ç
Á¶¼ºÁø ( Cho Seong-Jin )
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ °µ¿¼º½Éº´¿ø º´¸®Çб³½Ç
½ÅÇü½Ä ( Shin Hyung-Sik )
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ °µ¿¼º½Éº´¿ø º´¸®Çб³½Ç
±èÁÖ¼· ( Kim Joo-Seop )
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ °µ¿¼º½Éº´¿ø ¿Ü°úÇб³½Ç
±èµÎÁø ( Kim Doo-Jin )
ÇѸ²´ëÇб³ ÀÇ°ú´ëÇÐ °µ¿¼º½Éº´¿ø ¿Ü°úÇб³½Ç
KMID : 0357920100440020199
Abstract
Paraduodenal pancreatitis (PP) is a rare, distinct form of chronic pancreatitis, and it is related to alcohol abuse in middle-aged men. A 36-year-old man with a history of chronic recurrent pancreatitis for 4 years and alcohol abuse for 15 years presented with abdominal pain. Computed tomography revealed a multilocular cystic mass 3.2¡¿3¡¿3 cm in size and it was located within the muscular layer of the duodenal wall. The cysts were lined by a single layer of eosinophilic cuboidal epithelial cells that stained positively for mucin (MUC)1, MUC6, cytokeratin (CK)7 and CK19 and they stained negatively for MUC2, MUC5AC and CK5/6. Mild, chronic inflammatory reaction around the cystic wall, Brunner¡¯s gland hyperplasia and several clusters of heterotopic pancreatic tissue were noted. We report here on a case of PP and we demonstrated that the pancreatitis was of pancreatic ductal cell origin according to the MUC and CK expression patterns we observed on the immunohistochemical analysis.
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Pancreatitis;chronic;Pancreatic ducts;Cysts
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