1.Gangliocytic paraganglioma of the duodenum: a case report.
Guo-Cong WU ; Kang-Li WANG ; Zhong-Tao ZHANG
Chinese Medical Journal 2012;125(2):388-389
Gangliocytic paraganglioma of the duodenum is an extremely rare disease. Few cases have been reported in the literature from 1957 to 2010. We reported a 67-year-old man with gangliocytic paraganglioma of the duodenum.
Aged
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Duodenal Neoplasms
;
diagnosis
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Duodenum
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pathology
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Humans
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Male
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Paraganglioma
;
diagnosis
2.A Case of Easily Overlooked Small Duodenal Carcinoid Tumor.
Seung Young KIM ; Sung Woo JUNG ; Sang Woo LEE
The Korean Journal of Gastroenterology 2009;54(5):265-267
No abstract available.
Adult
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Carcinoid Tumor/*diagnosis/pathology
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Chromogranins/metabolism
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Duodenal Neoplasms/*diagnosis/pathology
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Duodenoscopy
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Humans
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Male
3.Duodenal Somatostatinoma: A Case Report and Review.
Jung A KIM ; Won Ho CHOI ; Chul Nam KIM ; Young Soo MOON ; Sun Hee CHANG ; Hye Ran LEE
The Korean Journal of Internal Medicine 2011;26(1):103-107
Somatostatinomas are rare functioning carcinoid tumors that usually arise in the pancreas and duodenum. They are seldom associated with typical clinical symptoms; their diagnosis is confirmed only by histological and immunohistochemical studies and the presence of specific hormones. Two distinct clinicopathological forms of somatostatinoma exist: duodenal and pancreatic somatostatinomas. Clinically, compared to pancreatic somatostatinomas, duodenal somatostatinomas are more often associated with nonspecific symptoms and neurofibromatosis, but less often with somatostatinoma syndrome or metastasis. Histologically, duodenal somatostatinomas frequently have psammoma bodies in the tumor cells. We report a case of duodenal somatostatinoma in 58-year-old man with vague epigastric pain and nausea. He did not have diabetes, steatorrhea, or cholelithiasis. Abdominal computed tomography showed a 25-mm mass in the duodenum and 25-mm nodule in the liver. Endoscopic retrograde cholangiopancreatography showed a duodenal submucosal tumor. Although the endoscopic biopsies were free of malignancy, the patient subsequently underwent Whipple's operation for the duodenal mass. Examination revealed as a somatostatinoma using a special stain for somatostatin.
Cholangiopancreatography, Endoscopic Retrograde
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Duodenal Neoplasms/diagnosis/*pathology/surgery
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Humans
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Male
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Middle Aged
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Somatostatinoma/diagnosis/*pathology/surgery
4.A Case of Gangliocytic Paraganglioma in Duodenum.
Jie Hyun KIM ; Hee Man KIM ; Si Young SONG ; Yoon Jae KIM ; Chang Hoon HAHN ; Seung Woo PARK ; Jae Bock CHUNG ; Jin Kyung KANG ; Woo Jung LEE ; Nam Hoon CHO
The Korean Journal of Gastroenterology 2004;43(1):47-51
Duodenal gangliocytic paraganglioma derived from neural crest is a peculiar neuroendocrine tumor. It is incidentally found during radiographic studies or due to gastrointestinal hemorrhage caused by frequent ulceration of the overlying mucosa. Most lesions are pedunculated and submucosal with distinctive histology consisting of endocrine cells, ganglion cells and spindle-shaped Schwann cells. We experienced a duodenal gangliocytic paraganglioma in a 40-year-old woman presenting with episodes of melena. Esophagogastroduodenoscopy revealed a submucosal ulcerated tumor in the second portion of duodenum and a biopsy confirmed gangliocytic paraganglioma. The tumor was enucleated through a duodenotomy. It's size was 5.5 X 3 X 1.5 cm sized and revealed positive cellular reaction for chromogranin, synaptophysin, neuron-specific enolase, and neurofilament by immunohistochemistry. The majority of the reported duodenal gangliocytic paraganglioma were of benign nature. Therefore, radical surgery or a lymph node dissection could be avoided if that disease was confirmed. However, thorough investigation for lymph node metastasis and postoperative follow-up are needed. We report the first case of a duodenal gangliocytic paraganglioma in Korea with a review of literature.
Adult
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Duodenal Neoplasms/*diagnosis/pathology/surgery
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English Abstract
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Female
;
Humans
;
Paraganglioma/*diagnosis/pathology/surgery
5.Primary Duodenal Choriocarcinoma Presenting as Massive Intestinal Bleeding and Metastasis to Brain.
Eun Young CHO ; Chang Soo CHOI ; Ji Woong KIM ; Ji Hye KWEON ; Tae Hyeon KIM ; Geom Seog SEO ; Hyang Jeong JO ; Suck Chei CHOI ; Yong Ho NAH
The Korean Journal of Gastroenterology 2006;48(2):128-131
Duodenal choriocarcinoma, either primary or metastatic, is very rare. Early diagnosis and prompt initiation of chemotherapy improve the prognosis of this neoplasm. We herein present, together with the referred literatures, a case of a 47-year-old female patient who visited to our hospital with upper intestinal bleeding. She was diagnosed as duodenal choriocarcinoma by operation. Brain metastasis was found soon after the operation and combination chemotherapy was done.
Brain Neoplasms/*secondary
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Choriocarcinoma/*diagnosis/secondary
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Duodenal Neoplasms/*diagnosis/pathology
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Female
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Gastrointestinal Hemorrhage/*diagnosis
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Humans
;
Middle Aged
6.Clinical characteristics and surgical treatment of 18 cases of duodenal gastrointestinal stromal tumors.
Yi-Hong SUN ; Xue-Fei WANG ; Ying-Yong HOU ; Xin-Yu QIN
Chinese Journal of Gastrointestinal Surgery 2007;10(1):26-28
OBJECTIVETo investigate the clinical characteristics, surgical procedures and prognosis of duodenal gastrointestinal stromal tumors (GISTs).
METHODSThe clinical data of 18 GIST patients, collected from 1995 to 2004, were retrospectively analyzed.
RESULTSThe lesions of duodenal GISTs mainly located in the descending duodenum (13/18), unusually in the horizontal part (2/18), ascending part (1/18), and the bulb (2/18). Pathological examination revealed 1 case of benign tumor, 2 cases of borderline tumors and 15 cases of malignant tumors, Microscopically, the tumors were composed of spindle cells (14 cases), epithelial cell (1 case), and mixed cell types (3 cases). The clinical manifestations were non-specific, mostly was melena (7/18), as well as abdominal pain (6/18), fullness (5/18), and anemia (3/18). The diagnoses were performed by upper gastrointestinal radiography, gastroscopy, endoscopic ultrasonography and CT scan. All of the 18 patients received surgical treatment, including 9 pancreaticoduodenectomies, 5 local resections, 3 segmental resections of duodenum, and 1 distal subtotal gastrectomy. 1 and 3 year survival rates were 100% and 86.7% respectively.
CONCLUSIONMost duodenal GISTs are malignant, and the choices of surgical procedures are mainly determined by the location and size of the tumors.
Adult ; Aged ; Duodenal Neoplasms ; diagnosis ; pathology ; surgery ; Female ; Gastrointestinal Stromal Tumors ; diagnosis ; pathology ; surgery ; Humans ; Male ; Middle Aged ; Retrospective Studies
7.A Case of Small Duodenal Carcinoid Tumor with Liver Metastasis.
Jai Hoon YOON ; Oh Young LEE ; Seung Chul CHO ; Hang Lak LEE ; Byung Chul YOON ; Ho Soon CHOI ; Soon Young SONG ; Seung Sam BAEG
The Korean Journal of Gastroenterology 2009;53(4):246-250
Carcinoid tumors are slow growing submucosal tumors with metastatic potential that arise from enterochromaffin cell. The annual incidence of carcinoid tumor is 2 to 3 per 100,000. Carcinoid tumor of duodenum is very rare with an incidence of about 8% among gastrointestinal carcinid tumor. As a endoscopic examination and immnohistochemical stain are developed, an rate of detection is increasing. Among the possible factor of metastatic prediction, tumor size >10 mm, central depression or ulcer, invasion below submucosa, lymphatic or venous invasion are associated with higher metastatic potential. Specially, in case of tumor size <10 mm, in duodenum, there is no report of metastasis to liver in Korea. But, recently, we experienced a rare care of duodenal carcinoid measured by less than 10 mm with liver metastsis. Thus, we report here this case with a review of literature.
Aged, 80 and over
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Carcinoid Tumor/*diagnosis/pathology
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Diagnosis, Differential
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Duodenal Neoplasms/*diagnosis/pathology
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Female
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Humans
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Liver Neoplasms/diagnosis/pathology/*secondary
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Neoplasm Metastasis
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Tomography, X-Ray Computed
9.Diagnosis and treatment of benign duodenal tumor.
Zhi-ming HU ; Shou-chun ZOU ; Da-jian ZHAO ; Cheng-wu ZHANG ; Dun SHI ; Zai-yuan YE ; Yang-ping JIANG
Chinese Journal of Gastrointestinal Surgery 2005;8(1):35-37
OBJECTIVETo investigate the diagnosis and treatment of benign duodenal tumor.
METHODSClinical data of 14 patients with benign duodenal tumor confirmed pathologically or by operation from Oct.1988 to Oct.2001 were analyzed retrospectively.
RESULTSOf 14 patients, 5 had Brunner's grand adenoma, 4 mesenchymoma, 2 leiomyoma, 2 hemangioma, 1 lipoma. Upper abdominal discomfort (64% ), gastrointestinal bleeding(50% ) and abdominal pain(20% ) were common manifestations. All cases received gastroscopy and only one case was diagnosed. Five cases received duodenoscope and the diagnosis was confirmed in 4 cases. Nine cases received hypotonic duodenography and lesions were found in 8 cases. Digital subtraction angiography was performed in 3 cases and detected all lesions. Computed tomographic scan and B-ultrasound were performed in 2 cases and only one case was diagnosed. Eleven cases (79% ) got definite diagnosis before operation. Tumor resection was performed in all patients. Perioperative death occurred in one patient. No recurrence occurred in 13 cases after following up from 2 to 11 years.
CONCLUSIONUpper abdominal discomfort and gastrointestinal bleeding are common features in patients with benign duodenal tumor. Duodenoscopy and hypotonic duodenography are good diagnostic approaches. Surgical tumor resection is the first choice of treatment.
Adult ; Aged ; Duodenal Neoplasms ; diagnosis ; pathology ; surgery ; Duodenoscopy ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Retrospective Studies
10.Primary Duodenal MALT Lymphoma.
Dae Ik NAHM ; Il Hyun BAEK ; Myung Seok LEE
The Korean Journal of Gastroenterology 2007;49(6):343-345