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Annals of Vascular Surgery | 1986

Arterial Manifestations in Behçet's Disease: Four New Cases

Moktar Dhobb; F. Ammar; Younes Bensaid; A. Benjelloun; Taoufik Benabderrazik; Benacer Benyahia

Four new arterial lesions observed with Behçets disease are reported: two popliteal aneurysms, one carotid aneurysm and one carotid stenosis. The clinical features, therapeutic modalities and postoperative complications of these uncommon lesions are reviewed briefly.


World Journal of Surgical Oncology | 2015

Venous thromboembolism in cancer patients: an underestimated major health problem

Jihane Khalil; Badr Bensaid; Hanan Elkacemi; Mohamed Afif; Younes Bensaid; Tayeb Kebdani; Noureddine Benjaafar

Venous thromboembolism (VTE) is a major health problem among patients with cancer, its incidence in this particular population is widely increasing. Although VTE is associated with high rates of mortality and morbidity in cancer patients, its severity is still underestimated by many oncologists. Thromboprophylaxis of VTE now considered as a standard of care is still not prescribed in many institutions; the appropriate treatment of an established VTE is not yet well known by many physicians and nurses in the cancer field. Patients are also not well informed about VTE and its consequences. Many studies and meta-analyses have addressed this question so have many guidelines that dedicated a whole chapter to clarify and expose different treatment strategies adapted to this particular population. There is a general belief that the prevention and treatment of VTE cannot be optimized without a complete awareness by oncologists and patients. The aim of this article is to make VTE a more clear and understood subject.


Annals of Vascular Surgery | 2009

Tuberculosis of the renal artery: a rare cause of renovascular arterial hypertension.

Zakariyae Bouziane; Khalil Boukhabrine; Zineb Lahlou; A. Benzirar; Omar El Mahi; B. Lekehal; Abbes El Mesnaoui; Younes Bensaid

Tuberculosis is an endemic disease in Morocco. Main blood vessels are rarely affected; the few mentioned cases are aneurysmal. We report a 17-year-old patient presenting with renovascular arterial hypertension, revealed thanks to the discovery of an occlusion of the right renal artery in Duplex scan. During the intervention, the observation of pararenal and mesenteric tuberculous polyadenopathy let us suggest the same kind of lesion at the level of the occluded renal artery. Once antituberculosis treatment had been carried out, the right renal artery was revascularized with a right iliorenal bypass using reversed internal saphenous vein. The postoperative course was uneventful, with an 18-month follow-up. Arterial pressure was normal without antihypertensive treatment, and the bypass was patent. As far as we know, this is the first case of renovascular arterial hypertension resulting from tuberculosis treated with an iliorenal bypass.


Annals of Vascular Surgery | 2011

Successful Endovascular Management of Postoperative Arterio Portal Fistula

Zakariyae Bouziane; Badr Ghissassi; M. Bouayad; Yasser Sefiani; B. Lekehal; Abbes El Mesnaoui; Younes Bensaid

Arterioportal fistulas are rare and mostly a result of late complication of gastric and biliary surgery. Surgical excision has been the therapy of reference. Endovascular treatment is emerging as a real alternative to surgery. The present study reports a case of postsurgical arterioportal fistula involving the gastroduodenal artery, the cause of portal hypertension, which was successfully treated by transarterial embolization using embospheres. Portal hypertension improved dramatically.


Annals of Vascular Diseases | 2011

Ruptured Tuberculous False Aneurysm of the Abdominal Aorta: A Case Report

A. Mechchat; B. Lekehal; Abbes El Mesnaoui; Fannid Ammar; Younes Bensaid

Tuberculous false aneurysm of the aorta is rare and has an unpredictable complication of aneurysm rupture. We report a case of a 32-year old woman who was referred to the Department of Vascular Surgery, Avicenne Hospital for severe abdominal pain. Chest x-ray revealed miliary tuberculosis. Contrast enhanced computed tomography (CT) scan showed a false aortic aneurysm involving the juxtarenal aorta. Antituberculous treatment was started because of high presumption of tuberculosis. Five days later, the patient presented with symptoms of aneurysm rupture. She underwent an emergency a surgical resection of the aneurysm with repair of the aortic wall defect by a Dacron Silver patch. The histopathologic examination of the aortic wall showed features of tuberculosis.


Journal Des Maladies Vasculaires | 2014

Association exceptionnelle d’un anévrysme poplité bilatéral et d’un anévrysme de l’aorte abdominale au cours d’un syndrome de Marfan

Y. Tijani; A. Mameli; H. Chtata; M. Taberkant; B. Lekehal; Y. Sefiani; A. Elmesnaoui; F. Ammar; Younes Bensaid; B. Feito; F. Bellenot; A. Fallouh; E. Cheysson

Marfan syndrome is an autosomal dominant disorder with rheumatoid, ophthalmological, neurological, cutaneous and cardiovascular manifestations. Aneurysmal lesions affecting both the abdominal aorta and the peripheral arteries are not often described in the literature. We report a case associating a bilateral popliteal aneurysm and an aneurysm of the infra-renal abdominal aorta.


Presse Medicale | 2008

Anévrisme de l’artère hépatique

Younes Bensaid; Badre Rhissassi; Nabil Sedki; Redouane El Idrissi; Samir El Khloufi; Omar El Mahi; Mustapha Alaoui; B. Lekehal; Yasser Sefiani; Abbas El Mesnaoui; F. Ammar

INTRODUCTION Aneurysms of the hepatic artery are relatively rare. Diagnosis often occurs only after rupture, and mortality is substantial. We report two new cases. CASES The first patient was a 70-year-old woman whose asymptomatic aneurysm of the common hepatic artery was identified during ultrasound for vomiting and abdominal pain. Open aneurysm repair and a hepatosplenic bypass led to a favorable outcome. The second patient was a 54-year-old man; his right hepatic artery aneurysm was diagnosed after it ruptured in the gall bladder. DISCUSSION We review the literature about hepatic artery aneurysms and discuss the clinical features and methods for diagnosis and treatment of these uncommon lesions.


Annals of Vascular Surgery | 2018

False Aneurysm of the Popliteal Artery Complicated by a Deep Venous Thrombosis Revealing an Exostosis in a 20-Year-Old Woman

Tarik Bakkali; Mohamed Hormatallah; Ayoub Bounssir; Nabil Aghtoutane; Hamza Taous; Redouane El Idrissi; Yasser Sefiani; Brahim Lekhel; Abbes El Mesnaoui; Younes Bensaid

Exostoses or osteochondromas are benign osseous tumors that develop on the bone surface and can be sporadic or hereditary. Their evolution is generally benign, but they may be complicated in some patients by conflicts with the surrounding nervous or vascular structures, in particular arteries. We report a case of false aneurysm of the popliteal artery secondary to an isolated exostosis of the left femur in a 20-year-old woman. A delay in the diagnosis allowed the development of the false aneurysm, which was at the origin of a major venous compression. The surgical treatment consisted in aneurysmectomy and reconstruction by end-to-end anastomosis associated with the resection of the osseous tumor, and the deep venous thrombosis was treated medically.


Journal of Medical Case Reports | 2017

Double localization of a non-anastomotic pseudoaneurysm after an axillofemoral bypass: a case report and review of the literature

Badr Bensaid; Tarek Bakkali; Y. Tijani; Samir Elkhalloufi; B. Lekehal; Y. Sefiani; Abess El Mesnaoui; Younes Bensaid

BackgroundA traumatic non-anastomotic pseudoaneurysm is a rare complication of an axillofemoral bypass graft. Fewer than 20 cases have been reported in the literature. Our case is unusual in that we report a double localization of this complication.Case presentationWe report the case of a 60-year-old Arabic male patient who was diagnosed with two hematomas in the trajectory of his axillofemoral bypass secondary to a traumatism. The diagnosis of a non-anastomotic pseudoaneurysm was retained considering the results of a computed tomography angiography scan, which showed the double localization of the pseudoaneurysm. Surgical management consisted of flattening the pseudoaneurysm along with the interposition of a prosthetic segment. There were no postoperative complications and our patient was well 3 years after discharge.ConclusionsNon-anastomotic pseudoaneurysm is a rarely described complication of a axillofemoral bypass graft. To the best of our knowledge, a double localization has not been described in the literature before. Minimally invasive techniques as a treatment option are being widely used as an alternative to open repair.


Annales De Biologie Clinique | 2017

Anévrisme infectieux des deux artères iliaques primitives : localisation rare d’infection à Salmonella typhimurium

Anass Rochdi; Othman Zahdi; Karim Souly; Y. Tijani; Youness Mechal; Nada Benjelloun; B. Lekehal; Y. Sefiani; Abbes El Mesnaoui; Younes Bensaid; Mimoun Zouhdi

Infectious aneurysm is a severe entity of the aneurysmal pathology, due essentially to a bacterial agent. The most frequently implicated organisms are salmonella and staphylococci. We report the case of an infectious aneurysm of the two primitive iliac arteries with Salmonella typhimurium in a 70-year-old man.

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Y. Tijani

Mohammed V University

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