Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Haykel Bedioui"'
Publikováno v:
Annales de Chirurgie. 129:293-296
Lymphoepithelial cyst of the pancreas is a benign and rare pathology. Its histogenesis is still unknown. The diagnosis is difficult to establish before surgery. We report a new case of a 20-year-old woman admitted for abdominal pain and vomiting. Rad
Autor:
N Maala, M Bakhtari, Haykel Bedioui, K. Chatti, W. Said, N.A Gordah, Ammar Bouziani, Sami Chahbani, N Ben Abdallah, M. Ben Alaya
Publikováno v:
Annales de Chirurgie. 129:244-247
Encapsulating peritonitis is a chronic peritonitis leading to the constitution of the thick white nacred fibrosis membrane. It is a rare affection. Its physiopathology is poorly elucidated. Diagnosis is usually at operation. We report an unpublished
Autor:
Khouloud, Bouslama, Haykel, Bedioui, Ahmed, Saidani, Houcine, Maghrebi, Yacine, Ben Safta, Farah, Jokho, Zoubeir, Ben Safta
Publikováno v:
In Clinics and Research in Hepatology and Gastroenterology December 2013 37(6):e133-e135
Autor:
Rachid Ksantini, Haykel Bedioui, Monia Ben Messaoud, Kais Nouira, Mohamed Jouini, Emna Menif, Hend Belhiba, Olfa Azaiez
Publikováno v:
CardioVascular and Interventional Radiology. 30:1242-1244
Suppurative pylephlebitis is a rare condition with a significant mortality rate, ranging from 50% to 80%. We report a case of suppurative pylephlebitis complicating acute pancreatitis treated by percutaneous drainage in a 40-year-old woman. The patie
Autor:
Maher Ben Reguigua, Amina Mekni, Haykel Bedioui, Mohamed Jouini, Faouzi Chebbi, Sofiane Baccar, Kais Nouira, Emna Menif
Publikováno v:
European Journal of Radiology Extra. 58:35-37
Malakoplakia of liver is rare and only five cases have been reported thus far. We report a case of liver malakoplakia in a 16-year-old female patient explored by ultrasonography, CT-scan and MRI. The diagnosis was made by needle core biopsy and the p
Autor:
Saddik Oueslati, Meher Ben Reguigua, Besma Laabidi, Haykel Bedioui, Nejmeddine Ben Abdallah, Mohamed Alaya, Kais Nouira, K. Chatti
Publikováno v:
Gastroentérologie Clinique et Biologique. 30:317-319
Resume Les tumeurs fibreuses solitaires (TFS), sont des tumeurs mesenchymateuses rares, habituellement decrites au niveau de la plevre, mais pouvant se developper dans differentes localisations extra pleurales. Elles ont ete exceptionnellement decrit
Publikováno v:
La Tunisie medicale. 90(6)
Despite the growing number of therapeutic methods and the recent introduction of new drugs more active in the therapeutic arsenal, lesions of the ano-perineal Crohn's disease remains difficult to support. Hyperbaric oxygen (HBO) was made before the e
Autor:
Wael, Rebai, Rachid, Ksantini, Amin, Makni, Faouzi, Chebbi, Oussama, Baraket, Fathia, Ben Hariz, Sofiene, Ayadi, Amine, Daghfous, Fadhel, Fterich, Haykel, Bedioui, Mohamed, Jouini, Montasser, Kacem, Zoubeir, Ben Safta
Publikováno v:
La Tunisie medicale. 89(3)
Intra ductal papillary mucinous tumors of pancreas are rare and are characterized by a risk of malignant transformation.To clarify their clinical presentation and the performance of different imaging examinations to determine their benign or malignan
Autor:
Amine, Daghfous, Haykel, Bedioui, Oussama, Baraket, Lamia, Kallel, Sofiene, Ayadi, Mohamed, Jouini, Montasser, Kacem, Zoubeir, Bensafta
Publikováno v:
La Tunisie medicale. 88(12)
Panniculitis mesenteritis is a rare, benign, and chronic fibrosing inflammation disease with unknown aetiology that affects the mesentery of small bowel and colon.To report a new case of this entity and to highlight its diagnostic difficulties especi
Autor:
Rachid Ksantini, Sofiene Ayadi, Wael Rebai, Haykel Bedioui, Mouna Mlika, Nidhameddine Khir, Amin Daghfous, Fadhel Fterich, Zoubeir Ben Safta, Faouzi Chebbi, Amin Makni, Mohamed Jouini, Montassar Kacem
Publikováno v:
Clinics and research in hepatology and gastroenterology. 35(5)
Acinar cell carcinoma (ACC) of the pancreas is a rare tumor with an extremely low incidence rate. While the number of reported patients with ACC is relatively small, a long-term survival rate has been noted in patients with neuroendocrine differentia