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Search Results: 1 - 10 of 464 matches for " Laila Chbani "
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Non Traumatic Myositis Ossificans Mimicking a Malignant Neoplasm: A Case Report  [PDF]
Latifa Tahiri, Laila Chbani, Siham Tizniti, Abdelmajid Elmrini, Taoufik Harzy
Open Journal of Radiology (OJRad) , 2012, DOI: 10.4236/ojrad.2012.24019
Abstract: Myositis ossificans is a benign self limiting condition that usually related to trauma. Despite a clinically and histologically distinct entity, myositis ossificans still causes considerable difficulties in diagnosis. A 33-year-old Moroccan woman presented with a 2-month history of left inguinal inflammatory pain with limping gait, MRI examination suggested a malignant neoplasm such as soft tissue osteosarcoma. A diagnosis of myositis ossificans was made by incisional biopsy. Conservative management with clinical and radiological follow up of 19 months confirm the diagnosis. The symptoms resolved within seven months. Myositis ossificans should be considered by clinicians as a possible diagnosis for a soft tissue lesion.
Liponeurocytoma of the Cerebellum with Myoid Features  [PDF]
Chbani Laila, Badioui Ikram, Znati Kaoutar, Benzagmout Mohamed, Maaroufi Mustapha, Amarti Afaf
Open Journal of Pathology (OJPathology) , 2012, DOI: 10.4236/ojpathology.2012.22004
Abstract: We report an extremely rare tumor presenting with myoid features in the left cerebellum lobe in a 62-year-old man. This tumor consisted of medium to large round cells with focal lipomatous and myoid differentiation. Immunohistochemically, the tumor cells expressed synaptophysin, GFAP (glial fibrillary acidic protein) and focally desmin. From these findings, we concluded that this tumor was a liponeurocytoma with myoid features. To our knowledge, this is the second report of liponeurocytoma with myoid differentiation in the cerebellum.
Synovial Sarcoma of Hand Presenting as A Cystic Mass  [PDF]
Chbani Laila, Badioui Ikram, Shimi Mohamed, Daoudi Abdelkrim, Tizniti Siham, Mrini Abdelmajid, Amarti Afaf
Open Journal of Orthopedics (OJO) , 2012, DOI: 10.4236/ojo.2012.22012
Abstract: Synovial sarcoma is a rare mesenchymal tumor. It occurs predominantly in the extremities especially in the region of the knee. The localization in palm hand is rare. We report a case of a 23 year-old man who present a monophasic synovial sarcoma of the left hand which presented as a painless cystic nodule. A surgical excision was performed. The result was good without recurrence. The synovial sarcoma is a rare malignant neoplasm that should be considered in the differential diagnosis of spindle neoplasms of hand.
Quality assessment of intraoperative frozen sections: An analysis of 261 consecutive cases in a resource limited area: Morocco  [PDF]
Laila Chbani, Sekal Mohamed, Tawfik Harmouch, Hinde El Fatemi, Afaf Amarti
Health (Health) , 2012, DOI: 10.4236/health.2012.47068
Abstract: Purpose: To evaluate the accuracy and limits of a frozen section analysis in our department in order to develop a quality control. Materials and methods: all frozen sections reported at our department between 1st January 2010 and 31st December 2010, have been retrospectively evaluated. The frozen section results were compared to permanent paraffin section results. Results: Frozen sections and final diagnosis agreed in 95% and disagreed in 5% (13 cases), 6.6% of the cases were deferred (17 cases). The most common pathological processes encountered were presence/typing of neoplasm (85.4%) and assessment of surgical margins (7.3%). Conclusion: The accuracy of frozen sections diagnosis at our department can be interpreted as comparable with the most international quality control series and is valuable to assist surgeons in their decision.
Young patient with juvenile polyposis syndrome: A case report  [PDF]
Mounia El Yousfi, Bahija Benyachou, Adil Ibrahimi, Laila Chbani, Afaf Amarti
Open Journal of Gastroenterology (OJGas) , 2012, DOI: 10.4236/ojgas.2012.23022
Abstract: A case is reported here of juvenile polyposis in a 15- year-old girl. She was diagnosed upon the assessment of the dysenteric syndrome. Coloscopy and gastro- scopy had shown polyps of variable size whose histological study confirmed the hamartomatous character typical of the youthful non adenomatous polyps free of dysplasia. There was no localization in the small bowel. Coloprotectomy with ileoanal anastomosis was carried out in view of the importance of diarrhoea and the impacts on the general state of health.
Scrotal Skin Metastases of Renal Cell Carcinoma: A Case Report  [PDF]
Khadija Benhayoune, Hinde El Fatemi, Jamal El Fassi, Soufiane Mellas, Laila Chbani, Nawal Hammas, Taoufiq Harmouch, Hassan Farih
Case Reports in Clinical Medicine (CRCM) , 2015, DOI: 10.4236/crcm.2015.43020
Cutaneous metastasis from renal cell carcinoma is believed to be rare. We present a 66-year-old man operated for kidney cancer 20 years ago and has consulted for a scrotal lesion that had started 20 days. The physical examination revealed an erythematous lesion. A biopsy of the scrotal skin was made. We found a scrotal metastasis of renal cell carcinoma.
Inoperable Pancreatic Metastasis of Renal Cell Carcinoma: A Case Report and a Review of Literature  [PDF]
Hanae Bedoudou, Lamiae Boudahna, Adil Mai, Boubacar Efared, Said Ait Laalim, Laila Chbani, Youssef Alaoui Lamrani, Nawfel Mellas
Journal of Cancer Therapy (JCT) , 2017, DOI: 10.4236/jct.2017.82014
Abstract: Renal cell carcinoma (RCC) is a common cancer, but its pancreatic metastasis is unusual. We report a case of a 50-year-old male who was under the first line of treatment for a metastatic RCC since 2009. In August 2015, he showed up to the day unit with a cholestatic jaundice, and the investigations led to the discovery of a liver function alteration and a pancreatic mass. The biopsy of the inoperable mass revealed a RCC metastasis. The localization of this metastasis complicated the management of the disease due to haemorrhage and anemia. An embolization was performed to control the local complications. The patient was commenced on everolimus but with modest results forcing us to start exclusive palliative care.
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.
Pseudotumoral Colic Tuberculosis: A Rare Pathological Entity  [PDF]
Eddy Oleko Ekuke, Pierlesky Elion Ossibi, El Mahdi Benkoukous, Moussa Sylla, Boubacar Efared, Laila Chbani, Abdelmalek Ousadden, Khalid Mazaz, Khalid Ait Taleb
Surgical Science (SS) , 2016, DOI: 10.4236/ss.2016.712069
Abstract: Colic tuberculosis is rare even in countries endemic to Mycobacterium spp. Its incidence seems to be increasing over the last decade. Presentation in the form of abdominal mass is exceptional and often misdiagnosed as gastrointestinal tumor. The possibility of a colic involvement of this infection needs to be considered given the broad spectrum of clinical manifestations of TB infection. We present a case of pseudo colic tuberculosis in a 58-year-old patient with no 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.
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