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Search Results: 1 - 10 of 13322 matches for " El Bachir Benjelloun "
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Annular pancreas producing duodenal obstruction: A case report  [PDF]
Abdesslam Bouassria, Hicham Elbouhaddouti, Ouadii Mouaqit, El Bachir Benjelloun, Abdelmalek Ousadden, Khalid Mazaz, Khalid Ait Taleb
Open Journal of Gastroenterology (OJGas) , 2013, DOI: 10.4236/ojgas.2013.33032

Annular pancreas is a rare congenital anomaly characterized by the presence of ectopic pancreatic tissue surrounding the duodenum. This malformation is usually asymptomatic in adults, but can manifests as pancreatitis, duodenal stenosis, or duodenal or gastric ulceration. We report the case of a young patient of 18 years old hospitalized for epigastric pain and vomiting, in whom radiological investigations showed an annular pancreas. At operation, a complete obstruction of the duodenum between its first and second parts was found, caused by an annular pancreas. No other congenital anomaly of the intra abdominal organs was noted. A gastroenterostomy was performed. Both the rarity of this congenital abnormality and its successful correction by surgical means have prompted us to make the following presentation.

The four killers of Meckel′s diverticulum
Benjelloun El Bachir,Ankouz Amal,Mazaz Khalid,Taleb Khalid
Journal of Emergencies, Trauma and Shock , 2009,
Duplication iléale chez l’adulte révélée par une perforation
Hicham El bouhaddouti,Abdelmalek Ousadden,Youssef Alaoui Lamrani,Bachir Benjelloun
Pan African Medical Journal , 2010,
Abstract: Les duplications intestinales sont des malformations digestives rares (0,2 % des malformations de l’enfant). Elles sont diagnostiquées généralement avant l’age d’un an, mais elles peuvent rester asymptomatiques et diagnostiquées à l’age adulte. Le diagnostic est fait le plus souvent lors de laparotomie faite en urgence devant une complication. Elles sont traitées par résection chirurgicale.
Common Bile Duct Cysts Leading to Cholestasis and Jaundice: A Rare Case Report  [PDF]
El Mahdi Benkoukous, Pierlesky Elion Ossibi, Zacharia Traore, El Bachir Benjelloun, Saeed Abdul-Razak, Kassim Sidibe, Youssef Lamrani, Abdelmalek Oussaden, Khalid Mazaz, Khalid Ait Taleb
Surgical Science (SS) , 2015, DOI: 10.4236/ss.2015.67044
Abstract: Cystic dilatation of the common bile duct constitutes a rare congenital malformation prevalent in people of Asian origin with a female predominance. Its classification follows that of Todani. The commonest form, found in 80% of cases, is type I. Common bile duct cysts are often diagnosed in 2 out of 3 cases, during childhood with adult forms often rare. We hereby report the case of a cystic dilatation of the bile duct in a 75-year-old patient without significant history of disease.
Colo-Colic Invagination on Lipoma  [PDF]
Eddy Oleko Ekuke, Pierlesky Elion Ossibi, Ouadii Mouaqit, El Bachir Benjelloun, Hicham El Bouhaddouti, Boubacar Efared, Laila Chbani, Abdelmalek Ousadden, Khalid Mazaz, Khalid Ait Taleb
Surgical Science (SS) , 2017, DOI: 10.4236/ss.2017.84022
Abstract: Intussusception in adults is rare and accounts for 1% to 5% of cases of acute bowel obstruction. Moreso, colic intussusception remains exceptional in adults and is usually secondary to an endoluminal lesion. Abdominal intestinal lipomas are rarely responsible for colonic invagination. They are often located on the caecum or the ascending colon and rarely on the left colon. We report the case of colo-colic invagination on a descending colon lipoma in a 50-year-old woman.
Pregnancy with Gastric Stromal Tumor  [PDF]
Iliass Charif, Najat Khalil, Abdelmalek Ousadden, El Bachir Benjelloun, Ouafae Slimani, Fatima Zahra Fdili Alaoui, Fatima Zahra Hijri, Omar Mesbahi, Adil Ibrahimi, Ihsane Mellouki
Case Reports in Clinical Medicine (CRCM) , 2014, DOI: 10.4236/crcm.2014.311124
Abstract: Background: Gastrointestinal stromal tumors (GIST) are the most common mesenchymal tumors of the gastrointestinal tract. GIST are rare during pregnancy. We report here the case of a patient who was admitted in our university hospital for GIST discovered during the second trimester of pregnancy. She was 42 years old, in the fifth months of pregnancy. She was admitted for biliary colic pain with vomiting. On abdominal examination, we objectified a distended abdomen with uterine height of 18 cm and epigastric mass of 10 cm. Abdominal ultrasound and magnetic resonance imaging (MRI) showed a hepatic, tissue and cystic mass, developing at the expense of the left liver. Endoscopy objectified an aspect of extrinsic compression at the front of the stomach. A cesarean was scheduled at the 35th month of pregnancy for fetal extraction and rescue. Exploration of the peritoneal cavity during surgery has objectified a hepatic highly vascularised mass reaching up to the umbilicus. This mass was unresectable. A postoperative CT scan revealed a large bilobed epigastric mass adhering to the stomach and the left liver. Histological and immunohistochemical study of hepatic process showed a gastrointestinal stromal tumor of high risk of malignancy. Conclusion: few cases have been reported in the literature on GIST during pregnancy showing the rarity of the condition that requires multidisciplinary care.
Retroperitoneal Smooth Muscle Tumor of Uncertain Malignant Potential (STUMP): Case Report  [PDF]
Moussa Sylla, Pierlesky Elion Ossibi, Issam Yazough, Eddy Oleko Ekuke, El Bachir Benjelloun, Said Ait Laalim, Khalid Mazaz, Khalid Ait Taleb
Surgical Science (SS) , 2016, DOI: 10.4236/ss.2016.712070
Abstract: Retro peritoneal smooth muscle tumors of uncertain malignant potential (STUMP) are rare and often misdiagnosed as leiomyosarcoma. We hereby report the case of a retroperitoneal STUMP diagnosed on a surgical specimen in a 44-year-old woman without any history of disease.
Pneumatose kystique iléale révélée par un volvulus du grêle
Hicham El bouhaddouti,Abdelmalek Ousadden,El Bachir Benjelloun,Karim Ibn Majdoub
Pan African Medical Journal , 2010,
Abstract: La pneumatose kystique intestinale est une pathologie rare qui se caractérise par la présence de kystes gazeux dans la paroi intestinale. Elle est asymptomatique ou pauci symptomatique, et le plus souvent découverte lors d’un examen d’imagerie ou d’endoscopie. Nous rapportons un cas de pneumatose iléale compliquée d’un volvulus sur bride chez un patient jamais opéré auparavant.
Small bowel intussusception with the Meckel's diverticulum after blunt abdominal trauma: a case report
El Bachir Benjelloun, Abdelmalek Ousadden, Karim Ibnmajdoub, Khalid Mazaz, Khalid Taleb
World Journal of Emergency Surgery , 2009, DOI: 10.1186/1749-7922-4-18
Abstract: Intususception is invagination of a proximal segment of bowel (intussusceptum) into the lumen of the adjacent distal segment (intussuscipiens). While intusussception is relatively common in the childhood, it is infrequently seen in adults [1]. Whereas most cases in childhood occur idiopathically, in adults, an underlying cause is present in 80% of cases [2]. Causes include tumours and polyps as well oedema and fibrosis from recent or previous surgery, and Meckel's diverticula. Cases following blunt abdominal trauma are rare. We present a case of 28-year previously healthy man presenting with abdominal pain and vomiting after blunt abdominal trauma, and developing four days later signs of small bowel obstruction as a cause of ileoileal intussusception with the Meckel's diverticulum. From an extensive review of the literature, intussusception at the site of a Meckel's diverticulum following blunt abdominal trauma has not been previously reported.A 28-year-old previously healthy man presented at the emergency department (ED) 48 hours after a hit in the left side of the abdomen by a fist, with gradual worsening of pain, nausea and bilious vomiting. Physical examination revealed a temperature of 37,6°C, a pulse rate of 80 beat per minute (bpm), a blood pressure of 110/70 mm Hg. The epigastrium, left upper and left lower abdominal quadrants were tender on palpation. On rectal examination the rectum contained no stool. Initial management of the patient involved intravenous fluid resuscitation, and nasogastric tube insertion, routine blood tests and supine abdominal x-rays. Initial laboratory values, including complete blood cell count, serum electrolytes, glucose, blood urea, creatinine, liver function tests, and lipase were all normal. Initially supine abdominal x-ray revealed dilated small-bowel loops with air-fluid levels, but no gas under diaphragm (Fig. 1). Ultrasonography (US) of the abdomen showed free fluid in the peritoneal cavity with dilated small bowel loops wi
Neuro Endocrine Tumor of the Gall Bladder: A Case Report  [PDF]
Eddy Oleko Ekuke, Yassine Kdhissi, Fatoumata Djouldé Smith Diallo, Pierlesky Elion Ossibi, Hicham El Bouhadoutti, El Bachir Benjelloun, Ouadii Mouaqit, Benajah Dafr-Allah, Abdelmalek Ousadden, Khalid Mazaz, Khalid Ait Taleb
Surgical Science (SS) , 2017, DOI: 10.4236/ss.2017.89046
Abstract: Neuroendocrine tumors (NET) of the gallbladder are a rare entity with only 0.2% of all NET located in the gall bladder. Well-differentiated NETs occur at a relatively lower age group unlike other gallbladder tumors, whereas neuroendocrine carcinoma (NEC) occurs in an older category of patients. The aim of our study is to discuss the current level of evidence regarding this pathological entity by means of a rare case report on a neuroendocrine carcinoma of the gall bladder in a 63-year-old patient with a history of diabetes. Patient underwent cholecystectomy for acute cholecystitis. Pathology findings on surgical specimen came back for neuroendocrine tumour.
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