1.Duodenal Obstruction due to Peptic Ulcer in Children.
Young Soo HUH ; Won Jong LEE ; Wook Dong KIM ; Bo Yang SUH ; Kwoing Bo KWUN
Yeungnam University Journal of Medicine 1989;6(1):43-46
Primary peptic ulcer disease in not known to be the result of underlying illness or trauma. These are most frequently duodenal or prepyloric. Since clinical features of peptic ulcer in children can easily be confused with many other disorders, the diagnosis is usually made when one of the more dramatic presentations, such as perforation, bleeding and obstruction. Recently, we experienced 2 cases of duodenal obstruction due to peptic ulcer in children. So, we report it with review of references.
Child*
;
Diagnosis
;
Duodenal Obstruction*
;
Hemorrhage
;
Humans
;
Peptic Ulcer*
2.A Case of Doudenal Diaphragm in an Adult Treated with Endoscopic Membranotomy using Insulated Tip Electrosurgical Knife.
Bum Jun KWON ; Chang Whan KIM ; Tae Ho KIM ; Yeon Soo LIM ; Jung Sun PACK ; Keun Jong CHO ; Jin Il KIM ; Soo Heon PARK ; Hiun Suk CHAE ; Jae Kwang KIM ; Sok Won HAN ; Kyu Yong CHOI
Korean Journal of Gastrointestinal Endoscopy 2006;33(5):294-297
A duodenal diaphragm is rare congenital anomaly among the duodenal obstructions. Its symptoms and signs usually appear from birth if the obstruction is complete. However, a diagnosis may be delayed until the patient reaches adulthood in cases of an incomplete obstruction. Treatment of an adult duodenal diaphragm is usually surgical. To our knowledge, there are few reports of the endoscopic treatment of an adult duodenal diaphragm but none in Korea. We report a duodenal diaphragm in a 26- year-old female with epigastric pain, who was treated with an endoscopic membranotomy using an insulated tip knife.
Adult*
;
Diagnosis
;
Diaphragm*
;
Duodenal Obstruction
;
Female
;
Humans
;
Korea
;
Parturition
3.A Case of Duodenal Web Associated with Intestinal Malrotation.
Jin Suk KIM ; Jhoo Taek LEE ; Jae Ock PARK ; Sang Mann SHIN
Korean Journal of Pediatric Gastroenterology and Nutrition 1999;2(1):99-103
Duodenal web is an uncommon lesion that infrequently cause partial or complete intestinal obstruction. If the duonenal web is incomplete and only partially obstructs the duodenal lumen, the onset of symptoms may be delayed for years, and obstructive symptoms will be only minimal and intermittent. Congenital duodenal obstruction is occasionally associated with intestinal malrotation. We experienced a case of duodenal web associated with intestinal malrotation in a 9-year-old girl who had been suffered from intermittent projectile vomiting since birth without failure to thrive. The diagnosis was made by UGI series & abdominal CT. Patient remained asymptomatic after operation.
Child
;
Diagnosis
;
Duodenal Obstruction
;
Failure to Thrive
;
Female
;
Humans
;
Intestinal Obstruction
;
Parturition
;
Tomography, X-Ray Computed
;
Vomiting
4.Endoscopic Diagnosis of Duodenal Stenosis in a 5-Month-Old Male Infant.
Maribeth R NICHOLSON ; Sari A ACRA ; Dai H CHUNG ; Michael J ROSEN
Clinical Endoscopy 2014;47(6):568-570
Duodenal stenosis and duodenal atresia are well-known gastrointestinal anomalies in patients with Down syndrome. Although duodenal atresia presents early and classically with vomiting in the immediate neonatal period, the presentation of duodenal stenosis can be significantly more subtle and the diagnosis delayed. Here, we describe the case of a 5-month-old male infant with Down syndrome and delayed presentation of high-grade duodenal stenosis diagnosed endoscopically. Pediatric gastroenterologists should include duodenal stenosis in the differential diagnosis of older infants and children with vomiting and should be familiar with the endoscopic appearance of this lesion.
Child
;
Constriction, Pathologic*
;
Diagnosis*
;
Diagnosis, Differential
;
Down Syndrome
;
Duodenal Obstruction
;
Hematemesis
;
Humans
;
Infant*
;
Male
;
Vomiting
5.Three Cases of Annular Pancreas in Adults.
Sung Joon LEE ; Moon Ki CHUNG ; Chang Duck KIM ; Hong Sik LEE ; Yoon Tae JEEN ; Jeong Seop MOON ; Jong Jae PARK ; Chi Wook SONG ; Ho Sang RYU ; Soon Ho UM ; Jai Hyun CHOI ; Jin Hai HYUN
Korean Journal of Medicine 1997;52(2):263-269
An annular pancreas consists of a band or ring of pancreatic tissue which surrounds the second portion of the duodenum is a rare congenital anomaly which may cause duodenal obstruction or remain silent throughout life. In an adult, symptoms from annular pancreas usually present between the ages of 20-50yr as duodenal obstruction. Peptic ulcer disease and pancreatitis may be found in association with symptomatic adult annular pancreas. The preoperative diagnosis of annular pancreas is often difficult. Although an upper gastrointestinal series is considered the diagnostic test, recognition is not always easy preoperatively. Recently, with the increased use of endoscopic retrograde cholangiopancreatography, patients with this anomaly were more frequently reported. In this report we describe two patients in whom the diagnosis of annular pancreas was clearly established by endoscopic retrograde cholangiopancreatography and one patient of suspected annular pancreas which was confirmed by surgery.
Adult*
;
Cholangiopancreatography, Endoscopic Retrograde
;
Diagnosis
;
Diagnostic Tests, Routine
;
Duodenal Obstruction
;
Duodenum
;
Humans
;
Pancreas*
;
Pancreatitis
;
Peptic Ulcer
6.A Case of Intramural Duodenal Hematoma Presenting with Acute Duodenal Obstruction.
Bong Jun HAN ; Bong Roung KIM ; Geun Young JANG ; Hyung Min KANG ; Hyung Don LEE ; Jae Eun PARK ; Su Hyun KIM ; Kye Heui LEE ; Jun Hyuk CHOI ; Yang Hun NAM
Journal of the Korean Geriatrics Society 2005;9(3):231-235
Intramural duodenal hematoma (IDH) is a quite rare disese entity which results from the collection of blood and body fluid between mucosa and serosa. Various degrees of duodenal obstruction may be caused by IDH as it gradually enlarges and compresses the mucosa against the opposite side of duodenum. The most common cause of IDH is blunt abdominal trauma and the spontaneous IDHs are generally casused by coagulation disorder such as blood dyscrasia, anticoagulation treatment or pancreaticoduodenal aneurysm. The diagnosis is usually made by the typical imaging on abdominal computed tomographic scan with a previous history of blunt abdominal trauma. For spontaneous IDH without coagulation disorder, an abdominal angiogram may be considered to exclude vascular anomalies. Medical treatment is recommended unless the associated visceral injuries require immediate laparotomy. Here, we report a case of acute duodenal obstruction due to IDH which had resolved completely without an operative management.
Aneurysm
;
Body Fluids
;
Diagnosis
;
Duodenal Obstruction*
;
Duodenum
;
Hematoma*
;
Laparotomy
;
Mucous Membrane
;
Serous Membrane
7.Organoaxial partial rotation of duodenum with midgut malrotation in an adult.
Luckshika Udeshani AMARAKOON ; Baj Gamage Anushka RATHNAMALI ; Jasin Arachchige Saman Bingumal JAYASUNDARA ; Ajith de SILVA
Singapore medical journal 2014;55(12):e191-3
Midgut malrotation includes a range of developmental abnormalities that occur during fetal intestinal rotation. Manifestations of intestinal malrotation are generally seen in the paediatric population and are uncommon in adults. Symptomatic patients may present with either acute abdominal pain due to midgut volvulus, or chronic abdominal pain due to proximal midgut partial obstruction in the presence of congenital bands. A limited number of paediatric cases of duodenal occlusion due to duodenal malrotation has been previously reported in the medical literature. We herein report the case of a 57-year-old woman who presented with duodenal obstruction due to organoaxial partial rotation of the distal duodenum associated with midgut malrotation. This is probably the first of such a case diagnosed in adulthood reported in the medical literature. Our patient underwent Roux-en-Y duodenojejunostomy and had symptomatic relief following the successful surgery.
Duodenal Obstruction
;
congenital
;
diagnosis
;
surgery
;
Duodenostomy
;
Duodenum
;
abnormalities
;
Female
;
Humans
;
Middle Aged
;
Sri Lanka
;
Treatment Outcome
8.Recurrent Pancreatitis Caused by Afferent Loop Syndrome with Pathologic Features of Type II Autoimmune Pancreatitis
Se Hee LEE ; Myung Hwan KIM ; Hae In KIM ; Ji Yeon BACK ; Yae Eun PARK ; Seung Mo HONG ; Hyung Jung KIM
Korean Journal of Medicine 2019;94(2):200-207
Afferent loop syndrome (ALS) is a rare cause of recurrent pancreatitis. Recurrent pancreatitis in association with ALS can develop due to impaired outflow of pancreatic juice or reflux of enteric secretions caused by increased intraluminal duodenal pressure. Here, we report a case of ALS presenting as recurrent acute pancreatitis due to chronic intermittent partial obstruction of the third portion of the duodenum caused by postoperative adhesion. Interestingly, pancreatic histology showed a granulocytic epithelial lesion, which is a diagnostic feature of type 2 autoimmune pancreatitis (AIP, idiopathic duct centric chronic pancreatitis [IDCP]). From this case we learned that the diagnosis of type 2 AIP should be made in the appropriate clinical setting.
Afferent Loop Syndrome
;
Diagnosis
;
Duodenal Obstruction
;
Duodenum
;
Pancreatic Juice
;
Pancreatitis
;
Pancreatitis, Chronic
9.Large Brunner's gland hamartoma with annular stricture causing gastric outlet obstruction.
In Tae HWANG ; Young Bum CHO ; Dong Eun PARK ; Keum Ha CHOI ; Tae Hyeon KIM
The Korean Journal of Internal Medicine 2016;31(2):392-395
No abstract available.
Adult
;
Biopsy
;
*Brunner Glands/pathology/surgery
;
Duodenal Diseases/*complications/diagnosis/surgery
;
Duodenal Obstruction/diagnosis/*etiology/surgery
;
Duodenoscopy
;
Gastric Outlet Obstruction/diagnosis/*etiology/surgery
;
Hamartoma/*complications/diagnosis/surgery
;
Humans
;
Male
;
Tomography, X-Ray Computed
;
Treatment Outcome
10.Duodenal Leiomyosarcoma Presenting with Gastrointestinal Bleeding and Obstruction: A Case Report
Seung Min HONG ; Gwang Ha KIM ; Dami KIM ; Sojeong LEE
The Korean Journal of Gastroenterology 2020;75(2):94-97
Duodenal leiomyosarcoma is a rare condition with a poor prognosis. Early diagnosis of duodenal leiomyosarcoma is challenging because it presents with nonspecific symptoms and endoscopic biopsies usually do not enable a definitive diagnosis. Duodenal leiomyosarcomas are diagnosed on the basis of the histopathological identification of a mesenchymal lesion composed of malignant tumor cells that on immunohistochemical examination is positive for smooth muscle actin and desmin. We report the case of a 38-year-old man who presented with gastrointestinal bleeding and obstruction who was diagnosed with duodenal leiomyosarcoma after surgical resection.
Actins
;
Adult
;
Biopsy
;
Desmin
;
Diagnosis
;
Duodenal Obstruction
;
Early Diagnosis
;
Gastrointestinal Hemorrhage
;
Hemorrhage
;
Humans
;
Leiomyosarcoma
;
Muscle, Smooth
;
Prognosis