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Search Results: 1 - 10 of 76 matches for " Imane Toughrai "
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Mirizzi Syndrome Complicating Acute Cholecystitis: CT Diagnosis  [PDF]
Kassim Sidibé, Pierlesky Elion Ossibi, Zacharia Traoré, Imane Kamaoui, Youssef Lamrani, Meryem Boubbou, Moustapha Maaroufi, Imane Toughrai, Khalid Mazaz, Siham Tizniti
Open Journal of Radiology (OJRad) , 2016, DOI: 10.4236/ojrad.2016.62013
Abstract: Mirizzi syndrome is a rare complication of gallstones with an incidence of less than 1% per year in Western countries. Imaging and endoscopy play a key role in its diagnosis. CT scan helps to eliminate any malignant lesion of the bile ducts or liver hence comes in handy in the confirmation of Mirizzi syndrome. We hereby report a case of a Mirizzi syndrome complicating acute cholecystitis in a 41-year-old patient without any history of disease.
Liposarcoma of the Spermatic Cord  [PDF]
Pierlesky Elion Ossibi, Hicham Anoune, Khalid El Haoudi, Karim Ibn Majdoub, Imane Toughrai, Said Ait Laalim, Khalid Mazaz
Case Reports in Clinical Medicine (CRCM) , 2014, DOI: 10.4236/crcm.2014.39113
Abstract: Few cases of Liposarcoma of the spermatic cord have been reported in the literature. This rare tumor represents 7% of malignant tumors of the spermatic cord. We report a case of an unusual liposarcoma of the spermatic cord, with respect to its sclerosing variant, occurring in a healthy looking 42 years old man. A wide local excision of the tumor was performed. Adjuvant radiotherapy may sometimes be effective on local recurrence. Even though this tumor evolves slowly, a prolonged follow up is required because of the risk of late recurrence.
Mixed Tumor of the Appendix: A Rare Tumor Association  [PDF]
Pierlesky Elion Ossibi, Mehdi Benkoukous, Abdoul Aliou Zabeirou Oudou, KarimIbn Majdoub, Imane Toughrai, Said AitLaalim, Khalid Mazaz
Surgical Science (SS) , 2014, DOI: 10.4236/ss.2014.510074
Abstract: Malignant tumors of the appendix are rare. They are present in 0.1% to 0.5% of appendectomy specimens: confirmed upon histological analysis. Mixed tumors in the appendix are exceptional. We report a mixed mucinous cystadenoma with a moderately differentiated adenocarcinoma of the appendix in a 64-year-old patient presented to the emergency room with bowel obstruction syndrome.
Adenocarcinoma of the Appendix  [PDF]
Moussa Sylla, Pierlesky Elion Ossibi, Somuah Tenkorang, Ismael Dandakoye, KarimIbn Majdoub, Imane Toughrai, Said Ait Laalim, Khalid Mazaz
Surgical Science (SS) , 2018, DOI: 10.4236/ss.2018.93012
Abstract: Objective: To report the experience of our department on adenocarcinoma of the appendix through a series of six (6) cases. Materials and Methods: This is a retrospective study carried out from January 2010 to June 2015 collating all cases of adenocarcinoma of the appendix diagnosed at the department of visceral surgery B in Hassan II University Hospital in Fez. Results: Six cases of adenocarcinoma of the appendix were recorded during the determined period of study. The mean age was 54.67 ± 16.99 years with the extreme ages ranging from 28 to 78 years. There was a female predominance with a sex ratio of 2. All patients had no specific medical history. The revealing symptoms were the following: appendicitis syndrome (1 case), bowel obstruction (1 case), psoas abscess (1 case) and fortuitous discovery during laparotomy for another problem (3 cases). The following histological types found were: colloid adenocarcinoma (3 cases), mucinous adenocarcinoma (2 case), mucinous cystadenocarcinoma associated with a moderately differentiated adenocarcinoma of the appendix (1 case). The surgical procedure consisted of a right hemicolectomy in 3 patients. Appendectomy followed by a right hemicolectomy and drainage of psoas abscess was performed in two patients. Palliative ileocecal resection and Bouilly-Volkmann ileocolostomy was performed in one patent who had carcinosis. All patients received adjuvant chemotherapy. The following occurred during follow-up: carcinosis (2 patients), a locoregional recurrence (2 patients). Two patients never returned for follow-up. Conclusion: Tumor of the appendix is a rare and exceptional pathology. These tumors are generally discovered fortuitously or during histology of appendectomy specimens. The treatment is usually surgical.
Hernie de Spiegel: a propos d un cas
Karim Ibn Majdoub Hassani,Fatimzohra Zahid,Hicham Anoune,Imane Toughrai
Pan African Medical Journal , 2010,
Abstract: La hernie de Spiegel ou hernie ventrale latérale est une déhiscence inhabituelle apparaissant sur la ligne ou fascia semi-lunaire de Spiegel. C’est une entité clinique rare, représente 0.10 à 1 pourcent des hernies. Aussi, nous a-t-il paru opportun de rapporter ce cas colligé dans le service de chirurgie B du CHU Hassan II de Fès. Nous rapportons l’observation d’une patiente agée de 60 ans, sans antécédent particulier qui présentais une tuméfaction para ombilicale gauche augmentant progressivement de volume, Une hernie de Spiegel a été suspectée à l’examen clinique, et le diagnostic d’éventration antérolatérale gauche a été retenu à la tomodensitométrie abdominale. Une cure de la hernie par plaque de prolène a été réalisée et les suites opératoires étaient simples. La hernie de Spiegel est une affection rare, son diagnostic clinique peut être difficile. Elle est asymptomatique dans 90 pourcent des cas et Son diagnostic positif est radiologique. Le risque d’étranglement non négligeable impose un traitement chirurgical une fois le diagnostic est confirmé.
Spontaneous Cholecystocutaneous Fistula of Anterior Abdominal Wall with Subcutaneous Gallstones: About a Rare Case and Review of the Literature  [PDF]
Khalid El Haoudi, Pierlesky Elion Ossibi, Salima Rezzouk, Mourad Oussaid, Karim Ibn Majdoub Hassani, Said Ait Laalim, Imane Toughrai, Khalid Mazaz
Surgical Science (SS) , 2014, DOI: 10.4236/ss.2014.52010

Spontaneous cholecystocutaneous fistula is a rare complication of chronic calculous cholecystitis, because currently gallstones are diagnosed and treated at an early stage. This occurrence is possible even if it seems actually to be rare. We report a case of spontaneous cholecystocutaneous fistula of Anterior Abdominal Wall with subcutaneous gallstones admitted in the medical oncology unit of HASSAN II University Hospital. An 64-year-old woman, presented with a large subcutaneous abscess in the right subcostal area with swelling. An abdominal computed tomography scan showed a subcutaneous gallstone and communication between the abscess and the gallbladder. Cholecystectomy was performed and the abdominal wall abscess was drained externally. This case report demonstrates that maintaining a high degree of suspicion of this rare entity is helpful in achieving correct preoperative diagnosis, and that computed tomography scan should be performed in all cases of unexplained abdominal wall suppuration.

Fasciitis on Abdominal Craniectomy Implantation  [PDF]
Pierlesky Elion Ossibi, Salima Rezzouk, Ibrahima Berete, KarimIbn Majdoub, Imane Toughrai, Said Ait Laalim, Abdelmalek Ousadden, Mohammed Chaoui El Faiz, Khalid Mazaz, Khalid Ait Taleb
Surgical Science (SS) , 2014, DOI: 10.4236/ss.2014.510073
Abstract: Necrotizing fasciitis is an infection of the skin and deep subcutaneous tissue. It is caused by bacteria (group A streptococcus), but may also be idiopathic ora secondary complication of surgery. We report a case of necrotizing fasciitis of the abdominal wall fostering a decompressive cranial flap in a 39-year-old patient.
Squamous Cell Carcinoma of the Pancreas  [PDF]
Pierlesky Elion Ossibi, Issam Yazough, Amal Bennani, KarimIbn Majdoub, Imane Toughrai, Said Ait Laalim, Abdelmalek Ousadden, Laila Chbani, Khalid Mazaz, Khalid Ait Taleb
Surgical Science (SS) , 2014, DOI: 10.4236/ss.2014.510075
Abstract: Exocrine pancreatic tumors are dominated by adenocarcinomas that have a poor prognosis. Squamous Cell Carcinoma of the pancreas is rare. We report a case of squamous cell carcinoma of the pancreas in a 75-year-old patient admitted to the emergency ward with acute cholangitis.
Hydatid Cyst of the Psoas: A Rare Location  [PDF]
Pierlesky Elion Ossibi, Issam Yazough, Saeed Abdul-Razak, Abdoul Aliou Zabeirou Oudou, Karim Ibn Majdoub, Imane Toughrai, Said Ait Laalim, Khalid Mazaz
Surgical Science (SS) , 2015, DOI: 10.4236/ss.2015.63019

Hydatid cyst of the psoas is rare even in countries endemic to hydatidosis. We hereby report a case of hydatid cyst of the psoas in a 69 years old patient with a history of hypertension and had received left nephrectomy due to a renal abscess 2 years prior to his admission.

Textiloma: A Case Report of Rectal Expulsion  [PDF]
Issam Yazough, Jean Marie Ovungu, Pierlesky Elion Ossibi, Franck Mvumbi, Said AitLaalim, Youssef Lamrani, Imane Toughrai, Karim Ibn Majdoub, Khalid Mazaz
Surgical Science (SS) , 2017, DOI: 10.4236/ss.2017.82010
Abstract: Textiloma is a rare pathological entity which can possibly complicate any surgery. Its incidence, reported in literature, is estimated between 1/1000 and 1/15,000. Abdominal and gynecological surgeries are responsible for the vast of majority of intra abdominal textiloma. Very few cases of spontaneous rectal expulsion of textiloma have been reported. We report the case of rectal expulsion of textiloma in a 26-year-old female who had undergone a C section for dynamic dystocia a year prior to her admission.
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