1.Intramural sparganosis manifested as intestinal obstruction: a case report.
Kyung Ja CHO ; Hyun Soon LEE ; Je G CHI
Journal of Korean Medical Science 1987;2(2):137-139
A case of intramural sparganosis of jejunum presenting as intestinal obstruction is described. Resected intestine from a 48 year old man with acute abdomen revealed a degenerated sparganum in the submucosa with typical tissue reaction and extensive edema. The tissue reaction was basically granulomatous, consisting of layers of inner palisading histiocytes and outer mononuclear cell infiltration. Many calcospherules were prominent within the degenerated worm. Eosinophil infiltration was scanty.
Granuloma/pathology
;
Humans
;
Intestinal Obstruction/*etiology
;
Jejunal Diseases/etiology
;
Male
;
Middle Aged
;
Sparganosis/*diagnosis
2.A Case of Inflammatory Fibroid Polyp Presenting with Jejunal Bleeding.
Man Keun HWANG ; Jung Hun KIM ; Sang Won PARK ; Jae Bum PARK ; Chang Ik LEE ; Chang Gu LEE ; Jin Kwan LEE
The Korean Journal of Gastroenterology 2003;42(4):337-340
Inflammatory fibroid polyp occurs very rarely in the jejunum and gastrointestinal bleeding as an initial manifestation of inflammatory fibroid polyp has not been reported. We report a case of a jejunal inflammatory fibroid polyp presenting with melena for 10 days. Upper gastrointestinal endoscopic examination was negative for any active bleeding lesions and abdominal angiography failed to localize the bleeding site as well. In contrast, computed tomography of the abdomen demonstrated a segmental wall thickening of the jejunum with a tumor-like mass lesion associated with dense contrast enhancement. Consistent with this, technetium 99m red blood cells scintigraphy exhibited red cell pooling at the right upper quadrant. On exploratory laparotomy, there was an active bleeding from the site of the jejunal tumor and a segmental resection was performed. Histologically, the tumor lesion of the jejunum was consistent with inflammatory fibroid polyp. Thus, we conclude that the tumor lesion was a cause of the gastrointestinal bleeding.
Adult
;
Gastrointestinal Hemorrhage/*etiology
;
Humans
;
Intestinal Polyps/diagnosis/*pathology
;
Jejunal Diseases/diagnosis/*pathology
;
Male
3.Intussusception Secondary to Jejunal Lymphangioma in a 13-year-old Girl.
Ho Sung PARK ; Ho LEE ; Woo Sung MOON ; Seung Chan LEE ; Woo Bong CHOI ; Hyun Woong CHOI
The Korean Journal of Gastroenterology 2007;49(4):256-259
Lymphangioma is a benign tumor composed of numerous small or large thin-walled lymphatic spaces. It shows a predilection for head, neck, and axilla. Jejunal lymphangioma in children is extremely rare. We present a case of 13-year-old girl with jejuno-jejunal intussusception secondary to lymphangioma in jejunum. To our knowledge, this is the second report of jejunal lymphangioma causing intussusception in a child.
Adolescent
;
Female
;
Humans
;
Intussusception/*etiology/surgery
;
Jejunal Diseases/*etiology/surgery
;
Jejunal Neoplasms/*complications/*diagnosis/pathology
;
Lymphangioma/*complications/*diagnosis/pathology
;
Tomography, X-Ray Computed
4.Primary Malignant Fibrous Histiocytoma (MFH) of the Small Bowel Presenting as an Intussusception Causing Small Bowel Obstruction.
Ung RYU ; Byung Wook LIM ; Jea Wook ROH ; Sang Eun LEE ; Hyun Bae SOHN ; Jeon Ho YANG ; Kyung Ah KIM ; June Sung LEE ; Young Soo MOON ; Han Seong KIM ; Woo Jin LEE
The Korean Journal of Gastroenterology 2004;44(2):99-102
Adult intussusception secondary to primary sarcoma is a rare cause of small bowel obstruction. Only a few cases of malignant fibrous histiocytoma (MFH) of small bowel presenting as an intussusception have been reported in the literatures. We report a case of small bowel obstruction associated with jejuno-ileal intussusception caused by MFH. A 75-year-old man was admitted with an one-month history of vomiting and epigastric pain aggravated with meals. He was diagnosed as an jejuno-ileal intussusception based on CT scanning and underwent small bowel resection and anastomosis. Resected specimens revealed a polypoid tumor in the ileum and the histology of the tumor was consistent with MFH.
Aged
;
English Abstract
;
Histiocytoma, Fibrous/*complications/diagnosis
;
Humans
;
Ileal Diseases/*etiology
;
Ileal Neoplasms/*complications/diagnosis
;
Intussusception/*etiology
;
Jejunal Diseases/*etiology
;
Male
5.Small Intestinal Perforation Caused by Primary Jejunal MALT Lymphoma.
Won Cheol JANG ; You Sun KIM ; Seong Woo HONG ; Yun Kyung KANG
The Korean Journal of Gastroenterology 2008;51(4):215-218
No abstract available.
Endoscopy, Digestive System
;
Female
;
Humans
;
Intestinal Perforation/*diagnosis/etiology/surgery
;
Jejunal Diseases/*diagnosis/etiology/surgery
;
Jejunal Neoplasms/complications/*diagnosis/pathology
;
Lymphoma, B-Cell, Marginal Zone/complications/*diagnosis/pathology
;
Middle Aged
;
Tumor Markers, Biological/analysis
6.A Case of Jejunal Infarction and Perforation due to Acute Pancreatitis.
Ji Young CHAI ; Su In YUN ; Sang Seok BAE ; Hee Bok CHAE ; Seon Mee PARK ; Sei Jin YOUN ; Jin Woo PARK ; Il Hun BAE ; Seok Hyung KIM ; Hyung Geun SONG ; Jun Ho WANG
The Korean Journal of Gastroenterology 2004;43(2):120-124
Jejunal infarction as a complication of acute pancreatitis is not common and can not be well recognized. This jejunal infarction usually arises from the venous thrombosis rather than arterial thrombosis. Jejunal infarction results in bowel perforation or stenosis according to its extension of injury and progression rate. Pathologic findings of the involved jejunum show a segmental transmural infarction and mesenteric venous thrombotic occlusions. Early diagnosis should be made for better prognosis. We report a patient with jejunal infarction resulting perforation due to acute pancreatitis, in which the initial presenting symptoms were hematemesis and abdominal distention.
Acute Disease
;
Adult
;
English Abstract
;
Humans
;
Infarction/diagnosis/*etiology
;
Intestinal Perforation/diagnosis/*etiology
;
Jejunal Diseases/diagnosis/*etiology
;
Jejunum/*blood supply
;
Male
;
Pancreatitis/*complications
;
Rupture, Spontaneous
9.A case of CMV disease of the jejunum in a patient with non-Hodgkin's lymphoma.
Ki Ju HAN ; In Seob JUNG ; Chan Kyu KIM ; Sung Kyu PARK ; Dong Won KIM ; Seung Ho BAICK ; Jong Ho WON ; Dae Sik HONG ; Seung Duk HWANG ; Chul MOON ; Hee Sook PARK
The Korean Journal of Internal Medicine 1998;13(2):143-146
CMV infection may occur anywhere in the gastrointestinal tract. Among the small intestine, ileum is the most common site of CMV disease and infection of jejunum is a rare one in patients with CMV gastroenteritis. Although rare, the reason why the recognition of this diagnosis is important is that it cause the lethal hemorrhage and perforation of gastrointestinal tract when its diagnosis and treatment was delayed. Rapid diagnosis are able to using the immunohistochemical stain in shell vial culture of infected specimen or peripheral neutrophils preparation in viremic patients within 8 to 36 hours. The treatment of choice is antiviral agent or surgical resection. We experienced a case of CMV disease of jejunum in patient with non-Hodgkin's lymphoma who showed severe ulceration in jejunum and massive intestinal hemorrhage, and he survived after successful treatment with segmental resection of jejunum and intravenous ganciclovir.
Adult
;
Antiviral Agents/therapeutic use
;
Cytomegalovirus Infections/drug therapy
;
Cytomegalovirus Infections/diagnosis
;
Cytomegalovirus Infections/complications*
;
Disease-Free Survival
;
Enteritis/virology
;
Enteritis/surgery
;
Enteritis/complications
;
Ganciclovir/therapeutic use
;
Gastrointestinal Hemorrhage/therapy
;
Gastrointestinal Hemorrhage/etiology*
;
Gastrointestinal Hemorrhage/diagnosis
;
Human
;
Jejunal Diseases/virology
;
Jejunal Diseases/surgery
;
Jejunal Diseases/complications*
;
Lymphoma, Non-Hodgkin/drug therapy
;
Lymphoma, Non-Hodgkin/diagnosis
;
Lymphoma, Non-Hodgkin/complications*
;
Male
;
Opportunistic Infections/drug therapy
;
Opportunistic Infections/diagnosis
;
Opportunistic Infections/complications*
;
Substances: Ganciclovir
;
Substances: Antiviral Agents
10.Chronic Non-granulomatous Ulcerative Jejunoileitis Assessed by Wireless Capsule Endoscopy.
Hyung Hun KIM ; You Sun KIM ; Kyung Sun OK ; Soo Hyung RYU ; Jung Hwan LEE ; Jeong Seop MOON ; Hyuck Sang LEE ; Hye Kyung LEE
The Korean Journal of Gastroenterology 2010;56(6):382-386
Chronic non-granulomatous jejunoileitis is a rare disease characterized by malabsorption, abdominal pain, and diarrhea that causes shallow ulcers in the small bowel. The etiology of chronic non-granulomatous jejunolieitis remains unknown. A 69-year-old man complained of abdominal pain and lower extremity edema. A 99m-Tc albumin scan showed increased radioactivity at the left upper quadrant, suggesting protein-losing enteropathy. A small bowel follow-through did not disclose any lesions. Wireless capsule endoscopy revealed several small bowel ulcers and strictures. A jejunoileal segmentectomy with end-to-end anastomosis was performed, and the histologic examination revealed non-granulomatous ulcers with focal villous atrophy. Ruling out all other possible diagnoses, we diagnosed our patient with chronic non-granulomatous ulcerative jejunoileitis. Postoperatively, the patient's abdominal pain and lower extremity edema improved, and the serum albumin normalized. This is the first case of chronic non-granulomatous ulcerative jejunoileitis localized by wireless capsule endoscopy and treated successfully with segment resection.
Abdominal Pain/etiology
;
Aged
;
Atrophy/diagnosis/etiology
;
Capsule Endoscopy
;
Chronic Disease
;
Diagnosis, Differential
;
Humans
;
Ileitis/*diagnosis/pathology
;
Intestine, Small/pathology
;
Jejunal Diseases/*diagnosis/pathology
;
Malabsorption Syndromes/diagnosis/pathology
;
Male
;
Mastectomy, Segmental
;
Protein-Losing Enteropathies/diagnosis
;
Technetium Tc 99m Aggregated Albumin/diagnostic use
;
Ulcer/pathology