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Search Results: 1 - 10 of 32 matches for " Pierlesky Elion Ossibi "
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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.
Rupture of Liver Hydatid Cyst into Gall Bladder  [PDF]
El Mahdi Benkoukous, Pierlesky Elion Ossibi, Hicham El Bouhadoutti, Said Ait Laalim, Abdelmalek Oussaden, Khalid Mazaz, Khalid Ait Taleb
Surgical Science (SS) , 2015, DOI: 10.4236/ss.2015.67045
Abstract: Hepatic hydatid cyst is a rare parasitic affection which constitutes a major health problem in countries endemic to hydatidosis. Rupture of hydatid cyst into gallbladder is an exceptional complication first described in 1952 by Atlas and Kamenear. We report the case of a hepatic hydatid cyst rupture into gallbladder in a 31-year-old patient with no history of disease.
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.
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
Abstract:

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
Abstract:

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.

A Case Study of Mesenteric Ischemia by Low Flow CT Imaging  [PDF]
Zacharia Traore, Pierlesky Elion Ossibi, Asmae Zeroual, Seydou Ly, Imane Kamaoui, Youssef Lamrani, Meryem Boubbou, Moustapha Maaroufi, Khalid Mazaz, Siham Tizniti
Open Journal of Radiology (OJRad) , 2015, DOI: 10.4236/ojrad.2015.51006
Abstract: Acute mesenteric ischemia is a serious disease whose prognosis depends on early diagnosis and therapeutic management. Recent imaging technics play a fundamental role in its diagnosis. There are many forms of mesenteric ischemia including the non-occlusive form which is rare among others. We report the case of a non-occlusive mesenteric ischemia by low flow in a patient with terminal renal disease placed on hemodialysis.
A Special Case of Renal Duplication Diagnosed on CT Imaging  [PDF]
Zacharia Traore, Pierlesky Elion Ossibi, Ababacar Traore, Saeed Abdul Razak, Youssef Lamrani, Meryem Boubbou, Moustapha Maaroufi, Khalid Mazaz, Siham Tizniti, Imane Kamaoui
Open Journal of Radiology (OJRad) , 2015, DOI: 10.4236/ojrad.2015.51007
Abstract: Renal duplication or supernumerary kidney (SK) is a rare anomaly, poorly documented. It is often discovered fortuitously or after complications. Its preoperative diagnosis is difficult. We hereby report the case of a left supernumerary kidney discovered upon thoracic-abdominal pelvic CT staging in a 50-year-old woman monitored for squamous cell carcinoma of the cervix.
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