1.Intrapancreatic accessory spleen: An eluding diagnosis
Teoh Keat How ; Balraj Singh ; Navarasi S Raja Gopal
The Medical Journal of Malaysia 2017;72(1):68-70
Intrapancreatic accessory spleen (IPAS) is a benign anomaly
of splenic embryology and a rare cause of pancreatic
pseudotumour. Here, we report a case of a 70-year-old Malay
lady whose IPAS was discovered incidentally during her
surveillance computed tomography for her underlying left
lower lung fibrosis. Radiologically, the lesion mimicked a
neuroendocrine pancreatic tumour and was only diagnosed
pathologically as IPAS after surgery. In conclusion,
recognising IPAS as a differential for enhancing pancreatic
mass allows us to exhaust all non-invasive diagnostic
means to diagnose this benign lesion. It will allow the patient
to avoid unnecessary surgery and its accompanying
complications.
Spleen
;
Splenectomy
;
Pancrelipase
2.Atypical manifestation of solid and papillary epithelial neoplasm of the pancrease: case report.
Jeong Ho KWAK ; Dong Chan LEE ; Hyung Mo KIM ; Sang Hyun BYUN ; Kyung Ho KIM
Journal of the Korean Radiological Society 1993;29(2):279-282
We report a rescently experienced case with atypical radiologic manifestation of solid and papillary epithelial neoplasm of the pancreas in a 37 years old female patient. The tumor had heavy calcification on its capsule wall and septa. Instead of the usual encapsulated lesion with partly solid and partly cystic-hemorrhagic components, the lesion consisted of numerous fine cavitations containing air without fluid component except focal abscess fluid.
Abscess
;
Female
;
Humans
;
Neoplasms, Glandular and Epithelial*
;
Pancreas*
;
Pancrelipase*
3.A case of solid and papilary tumor of pancreas.
Kyoung Bum KIM ; Hae Won CHEON ; Ji Hee PAK ; Kee Hyoung LEE ; Kwang Chul LEE ; Young Chang TOCKGO
Journal of the Korean Pediatric Society 1993;36(12):1765-1769
We report a cases of solid and papillary neoplasm of the pancreas, which is a rare pancreatic tumor. we described clinical characteristics, sonographic, computed tomographic and pathologic finding. The tumors had a smooth, enhanced capsule and variable architecture. The tumor was distributed tail of pancreas without local invasion. the origin of the tumor is probably from a multipotential stem cell of the pancreas. Neoplasm usually behave like a very low grade malignancy, so that complete removal is the treatment of choice for the tumor arising anywhere in the pancrease. This unusual tumor should be considered in the differential diagnosis of a young female with pancreatic mass.
Diagnosis, Differential
;
Female
;
Humans
;
Pancreas*
;
Pancrelipase
;
Stem Cells
;
Ultrasonography
4.Small cell carcinoma of pancrease.
Ha Guen LEE ; Kyeong Geun LEE ; Chan Kum PARK ; Kwang Soo LEE
Korean Journal of Hepato-Biliary-Pancreatic Surgery 2006;10(4):38-40
Small cell cancer commonly occurs in the lungs, but it is rarely found in other organs. Small cell cancer that occurs in the pancreas is rare and its progress very rapid, and most patoents' tumor has already spread by metastasis when it is discovered. Although this cancer has a poor prognosis, we report here on treating case with combined curative resection and chemotherapy and showed a good prognosis.
Carcinoma, Small Cell*
;
Drug Therapy
;
Lung
;
Neoplasm Metastasis
;
Pancreas*
;
Pancrelipase*
;
Prognosis
5.Nine Case of Congenital Variants of the Pancreatic Duct Diagnosed by ERCP.
Jin Kyung KANG ; In Suh PARK ; Jae Bock CHUNG ; Si Young SONG ; Key Joon HAN ; Jun Pyo JUNG
Korean Journal of Gastrointestinal Endoscopy 1994;14(3):343-348
Although variation is the rule with pancreatic duct morphology, certain variants occur as a result of altered embroological development. These ductal configurations, most striking deviations from the normal configuration, may be classfied according to alterations of embryological development. These congenital variants of pancreatic duct may be important for several reasons. First, the pseudomass effect of ductal anomalies can be mistaken for carcinoma by the inexperienced radiologists. Second, whether or not the anomaly is important, it is present in many patients with recurrent pacreatitis. Original descriptions were based on small sampling of postmortem studies and surgical specimen, but more recently the advent of endoscopic retrograde cholangiopancreatography(ERCP) has confirmed of the work of early anastomists and increased awareness of these variants. To evalute of frequency, characteristics of associated disease and clinical significance of pancreatic anomalies, we have reviewed of 5330 case of ERCP filmes which were undertaken between July, 1973 and August, 1993. Having reviewed of ERCP filmes, we found out 9 case of pancreatic duct variants. Among them, 7 cases were classified as ductal duplication anomalies, 4 cases of number variation, most, bifuricaiton and 3 cases of form variation, which were composed of loop, spiral and terminal N. Three cases of fusion anomalies were also noted, which were 2 cases of panceratic divisum and 1 case of incomplete pancreatic divisum. The associated diseases were 6 cases of bile duct and galbladder stones and 3 cases of pancreatic cancer. We could not find out the case of congenital anomalies as cause of obstructive pain and pseudomass effect.
Bile Ducts
;
Cholangiopancreatography, Endoscopic Retrograde*
;
Humans
;
Pancreatic Ducts*
;
Pancreatic Neoplasms
;
Pancrelipase
;
Strikes, Employee
6.In vivo Assessment for the Antioxidant Activity of the Calcium Channel Blocker Nicardipine in 3% Sodium-Taurocholate-induced Acute Pancreatitis.
Jung Jin SEO ; Hyung Geun LEE ; Jong Kwon PARK ; Jung Taik KIM ; Dong Kook PARK ; Min CHUNG ; IM Hwan ROE ; Mie Rha YANG
Journal of the Korean Surgical Society 1998;55(4):469-477
BACKGROUND: Although several pathophysiological sequences, such as protease activation, free radical generation, and inflammatory mediator release, have been described in acute pancreatitis, the precise mechanism by which acute pancreatitis is initiated is unkown. Cellular calcium, a key function and also a crucial pathological intracellular messenger in cell injury, appears to be involved in the initiation and development of acute pancreatitis. The aim of this study is to evaluate the role of cellular calcium and therapeutic effect of administering the Ca++ channel blocker nicadipine as an antioxidant. METHOD:Nicardipine, known to be a calcium channel blocker and a most potent antioxidant, was wed as a pretreatment 1 hour before induction of pancreatitis by intraductal infusion of 3% sodium taurocholate or as a post-treatment 1 hour after induction of aucte pancreatitis by retrograde infusion of sodium taurocholate. The net weight of the pancrease, the amounts of s-amylse, GSH and MDA in the pancreatic tissue, and the histologic damage were examined 12 hours after the induction of pancreatitis. RESULTS: Nicardipine administration ameliorated pancreatic edema and reduced the amount of s-amylase compare to untreated necrotizing pancreatitis group. Also, pre- or post-treatment with nicardipine had beneficial protective effect with respect to free radical-induced injury; in particular, pre-treatment with nicardipine was much better. With respect to the histologic findings, pancreatic necrosis, hemorrhage, and neutrophil infiltration were prominent in the necrotizing group, however, in the group treated with nicardipine, the necrosis and hemorrhage were ameliorated remarkably. CONCLUSION:The free oxygen radicals and the intracellular calcium influx were major elements in the pathogenesis of acute pancreatitis, and nicardipine ameliorated pancreatic necrosis and hemorrage and exerted an antioxidant effect. The administration of nicardipine should be considered in the early stage of pancreatitis or in case of risk of pancreatitis.
Antioxidants
;
Calcium Channels*
;
Calcium*
;
Edema
;
Hemorrhage
;
Necrosis
;
Neutrophil Infiltration
;
Nicardipine*
;
Pancreas
;
Pancreatitis*
;
Pancrelipase
;
Reactive Oxygen Species
;
Taurocholic Acid
7.Pancreatic Mucinous Ductal Ectasia A clinical study of four patients.
Tae Sung SOHN ; Jong Riul LEE ; Jae Hyung NOH ; Seong Ho CHOI ; Yong Il KIM ; Byung Boong LEE ; Jong Gyun LEE ; Soon Jin LEE ; Young Hye KO
Journal of the Korean Surgical Society 1998;54(5):756-764
Four cases of mucinous ductal ectasia of the pancreas are presented, along with a review of the literature. Mucinous ductal ectasia is a clinicopathologic entity characterized by dilation and filling of the main pancreatic duct or its side branches with thick, viscid mucus, leading to recurrent acute pancreatitis or symptoms that mimic chronic pancreatitis. Three of the patients were male (M:F=3:1) and the patients were 54~74 years old. The symptoms of two patients were abdominal pain and they had a frequent admission history due to pancreatitis. One patient had jaundice, and one patient presented no symptoms. In all of the patients, the tumor was located in the read of the pancrease and the size of tumor was about 3 cm. A total pancreatectomy was performed, and three pancreatico-duodenectomy were performed. The pathologic report revealed that two cases were malignant and two cases were borderline malignant. The tumor marker did not correlate with the presence of malignancy. Because mucinous ductal ectasia is recognized as a premalignant disease, the treatment of choice is pancreatic resection.
Abdominal Pain
;
Dilatation, Pathologic*
;
Humans
;
Jaundice
;
Male
;
Mucins*
;
Mucus
;
Pancreas
;
Pancreatectomy
;
Pancreatic Ducts
;
Pancreaticoduodenectomy
;
Pancreatitis
;
Pancreatitis, Chronic
;
Pancrelipase
8.Pancreatic Tuberculosis with Microcystic Adenoma.
Hak Youn LEE ; Sung Heun KIM ; Ki Jae PARK ; Young Hun KIM ; Jin Hwa LEE ; Mee Sook ROH
Journal of the Korean Surgical Society 2005;68(6):522-525
Tuberculosis of the pancreas is a rare disorder. The clinical presentation of pancreatic tuberculosis include nonspecific symptoms such as fever, fatigue and weight loss. The radiological features mimic pancreatic malignancy or pancreatitis. So, the diagnosis of pancreatic tuberculosis is very difficult. A 62-year-old man was referred for pancreatic mass. Findings on preoperative imaging modalities were consistent with pancreatic carcinoma, and fine needle aspiration test indicated microcystic adenoma or carcinoma. Pylorus-preserving pancreaticoduodenectomy was done. Final diagnosis was pancreatic tuberculosis combined with microcystic adenoma. We conclude in that patients who have a mass in the pancreas, pancreatic tuberculosis should be considered, particularly in the developing country and immunosuppressed individuals.
Adenoma*
;
Biopsy, Fine-Needle
;
Developing Countries
;
Diagnosis
;
Fatigue
;
Fever
;
Humans
;
Middle Aged
;
Pancreas
;
Pancreaticoduodenectomy
;
Pancreatitis
;
Pancrelipase
;
Tuberculosis*
;
Weight Loss
9.Laparoscopic Enucleation of a Pancreatic Mucinous Cystadenoma.
Ki Young YOON ; Eun Hee KONG ; Luca MILONE ; Michel GAGNER
Journal of the Korean Surgical Society 2005;69(2):181-185
We report a case of a 52-year-old man in whom a cystic pancreatic tumor was successfully removed by laparoscopic enucleation. The patient had a followup CAT-scan for a resolving right upper lobe pneumonia which demonstrated a unilocular hypodense 3.9x2.2 cm sized cyst in the uncinate process of the pancreas. He had a laparoscopic biliopancreatic diversion with duodenal switch in July 2002, and also had laparoscopic cholecystectomy for cholelithiasis in December 2003. Laparoscopic intraoperative ultrasonography revealed a solitary cystic tumor in the inferior portion of pancreatic head. Laparoscopic enucleation of the tumor was performed using Ultracision(R) between the cyst outer wall and the normal pancreatic parenchyma. The operative time was 160 minutes, the estimated blood loss was 20 ml, and there were no perioperative complications. The patient's postoperative course was uneventful, and he was discharged on the first postoperative day. The histopathologic diagnosis showed a mucinous cystadenoma. We reported a new technique for safe management of small cystic tumors located on surface of the pancreas.
Biliopancreatic Diversion
;
Bone Cysts
;
Cholecystectomy, Laparoscopic
;
Cholelithiasis
;
Cystadenoma, Mucinous*
;
Diagnosis
;
Follow-Up Studies
;
Head
;
Humans
;
Laparoscopy
;
Middle Aged
;
Mucins*
;
Operative Time
;
Pancreas
;
Pancrelipase
;
Pneumonia
;
Ultrasonography
10.Distrubution of gamma-Glutamyltransferase in Blood-Brain Barrier Pericytes Using Monoclonal Anti gamma-Glutamyltransferase Antibodies.
Byoung Kyu LEE ; Meyoung Kon KIM ; Kyu Man SHIN ; Chong Kun RYU
Journal of Korean Neurosurgical Society 1995;24(3):253-261
gamma-Glutamyltransferase(GGT: E.C. 2.3.2.2.) is a glycoprotein enzyme which is involved in glutathione metabolism and amino acid transport through the plasma membrane. It is distributed widely in several organs including liver, kidney, pancrease and brain. GGTs derived from the brain of Wister rats and BALB/c mice were biochemically purified to a specific activity of 4246.2, 862.1 units per mg of protein, a purification folds 93.7, 43.8 and the final yield 65.8, 44.0% respectively. Electrophoretic pattern of purified GGTs from rats and mice brain shows very similar protein fraction each other. We have produced six monoclonal antibodies(GGT-Mab 1-6) against 2-acetamidogluorene treated rat liver GGT. Using these GGT-Mab 1-6 we performed immunohistochemistry(IHC) to study the distribution of GGT isozymes in normal tissues of rat brain and in neoplastic tissues of human brain. The results indicated that human brain GGT was localized in pericytes of blood-brain barrier, especially in the blood-rich portion of the brain(e.g. cerebellum of rat, meningioma and craniopharyngioma of human). Therefore these Maps may be used to evaluate the distribution of GGT isozymes in different tissues.
Animals
;
Antibodies*
;
Antibodies, Monoclonal
;
Blood-Brain Barrier*
;
Brain
;
Cell Membrane
;
Cerebellum
;
Craniopharyngioma
;
gamma-Glutamyltransferase*
;
Glutathione
;
Glycoproteins
;
Humans
;
Isoenzymes
;
Kidney
;
Liver
;
Meningioma
;
Metabolism
;
Mice
;
Pancreas
;
Pancrelipase
;
Pericytes*
;
Rats