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11 results on '"Chaker, Jaber"'

1. Endovascular management of a ruptured popliteal artery aneurysm in a patient with Behçet's disease

Author

Chaker Jaber, Nadia Moulahi, Imtinene Ben Mrad, Mouna Bousnina, Amna Damak, Nadia Azabou, Mohamed Zairi, Amine Jemel, and Karim Kaouel

Subjects
Popliteal artery, Aneurysm, Behçet's disease, Diseases of the circulatory (Cardiovascular) system, RC666-701, Surgery, RD1-811
Abstract

Purpose: Popliteal artery aneurysms are the most common peripheral arterial aneurysms. One of their etiologies is Behçet's disease. Discussions about the best way to treat popliteal artery aneurysms in BD are still ongoing in the literature. We report a case of a patient that presented with a ruptured right popliteal artery aneurysm that had a successful endovascular treatment and was followed up for 36 months. Case report: Our patient was a 59-year-old male with a medical history of hypertension, diabetes mellitus and Behçet's disease. He presented with acute limb ischemia of the right lower limb. Doppler ultrasound showed a ruptured large aneurysm of 7,2 × 5,1 cm in size in the right popliteal fossa, compressing the popliteal artery. Digital subtraction angiography revealed a ruptured saccular aneurysm with a diameter of 7 cm of the popliteal artery. After heparin was administered intravenously, a Fluency™ 6 mm × 40 mm covered stent-graft was inserted. Final angiography showed a well positioned stent-graft excluding the aneurysm without any endoleak. The below-the-knee arteries were all patent. The symptoms of acute limb ischemia gradually disappeared and a surgical evacuation of the hematoma was performed five days after by internal popliteal approach. He was treated with Aspirin, Clopidogrel, Prednisolone and Azathioprine and followed up for 36 months without recurrence of symptoms. Conclusions: Endovascular stent-graft insertion in popliteal artery aneurysms in Behcet's disease might be a safe alternative to surgical intervention. Immunosuppressive therapy should precede the surgical or the endovascular intervention and should be continued after the procedure to avoid postoperative early and late complications.

Published
2022
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2. Cystic adventitial disease of the popliteal artery with unusual spontaneous regression: A case report with literature review

Author

Meriem Affes, Mohamed Chaabouni, Monia Attia, Chaker Jaber, Ines Baccouche, Salma Kchaou, Henda Nèji, and Saoussen Hantous‐Zannad

Subjects
adventitia, cysts, magnetic resonance imaging, popliteal artery, spontaneous remission, Medicine, Medicine (General), R5-920
Abstract

Abstract This report highlights the case of cystic adventitial disease of the left popliteal artery in a 45‐year‐old male patient. Imaging modalities confirmed the diagnosis and high resolution MRI found a cystic connection to the adjacent knee joint. The evolution was unusual with spontaneous regression of the symptoms.

Published
2022
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4. Abstracts of the Tunisian Society of Cardiology and Cardiovascular Surgery congress, STCCCV 2021

Author

Afef, Ben Halima, Hichem, Aouina, Agnès, Hamzaoui, Leila, Gharbi, Nawel, Chaouech, Besma, Dhahri, Hédia, Ghrairi, Sarah, Maazaoui, Imen, Sahnoun, Amani, Ben Mansour, Sabrine, Louhichi, Jihen, Ben Amar, Redha, Lakehal, Emna, Allouche, Habib, Ben Ahmed, Mohamed Selmen, Aissa, Marwa, Fathi, Feten, Boudiche, Hakim, Ben Jemaa, Mohamed, Béji, Wejdène, Ouechtati, Leila, Bezdah, Mohamed Aymen, Ben Abdessalem, Khalil, Cheikh Sidiya, Ahmed Fekih, Romdhane, Zied, Ben Ameur, Hamza, Mosrati, Fares, Ammar, Hatem, Bouraoui, Samia, Hajri, Abdallah, Mahdhaoui, Gouider, Jeridi, Khaoula, Nasser, Aymen, Elhraiech, Marouen, Kacem, Mohamed Ali, Tekaya, Ayoub, Meddeb, Khaldoun, Ben Hamda, Faouzi, Maatouk, Oussema, Wachem, Saoussen, Antit, Ridha, Fekih, Cyrine, Antit, Elhem, Boussabah, Moez, Thameur, Lilia, Zakhama, Soraya, Ben Youssef, Marwa, Ben Doudou, Sofien, Kamoun, Imtinene, Ben Mrad, Fathia, Ben Moussa, Sana, Fennira, Khedija, Mzoughi, Ihsen, Zairi, Sondes, Kraiem, Yosra, Messaoudi, Marwa, Ben Abdallah, Oumaima, Ghabi, Nejeh, Ben Halima, Sobhi, Mleyhi, Tarek, Sandi, Rim, Miri, Tesnim, Besbes, Faker, Ghédira, Skander, Ben Omrane, Raouf, Denguir, Mariem, Drissa, Asma, Brahim, Essia, Mousli, Cyrine, Ousji, Hassen, Abou Nada, Asma, Bouslimi, Amani, Merdassi, Oumaima, Taher, Habiba, Drissa, Wael, Yaakoubi, Manel, Ben Hlima, Bassem, Rekik, Med Amine, Soula, Fourat, Zouari, Slim, Boudiche, Fathia, Mghaieth, Sana, Ouali, Mohamed Sami, Mourali, Karima, Taamallah, Mariem, Abid, Nadhem, Hajlaoui, Aabdedeyem, Haggui, Wafa, Fehri, Moslem, Ben Abdallah, Fares, Azaiez, Nour, Cherif, Fakher, Jaoued, Rami, Tlili, Youssef, Ben Ameur, Ali, Khorchani, Zineelabidne, Ben Ali, Ala Eddine, Dali, Sami, Milouchi, Amine, Boufares, Iheb, Ben Krayen, Hichem, Mtimet, Mohamed Ghassen, Ben Haj Mbarek, Oussama, Bouhamed, Safa, Dardouri, Rym, Gribaa, Imen, Ben Ali, Mehdi, Slim, Elyess, Neffati, Emna, Damak, Chaker, Jaber, Taieb, Cherif, Mouna, Bousnina, Amine, Jemel, Sofiane, Jerbi, Yassine, Marzouki, Syrine, Neji, Mohamed, Beji, Imene, Chaabene, Soumeya, Tahri, Malek, Kechida, Syrine, Daada, Sonia, Hammami, Wajih, Ben Abdallah, Rim, Klii, Ines, Khochtali, Emna, Rekik, Marwa, Abdelhedi, Neji, Lahbib, Dorra, Aouadi, Souha, Abid, Boutheina, Besbes, Zeineb, Oumaya, Noufeil, BelKahla, Ibrahim, Arbaoui, Fatma, Daoued, Hela, Jebali, Ella, Lahmaier, Emna, Chaabouni, Mariem, Hajji, Mohamed Karim, Zouaghi, Maroua, Abdallah, Souheil, Mlayah, Yassine, Selmi, Hibar, Idriss, Jamel, Ahmed, Oumeima, Brahim, Elyes, Turki, Raja, Ghzel, Khalil, Ouaghlani, Kaouthar, Hakim, Amine, Boussema, Houda, Ben Arbia, Sana, Said, Hela, Msaad, Fatma, Ouarda, Roueida, Khalifa, Ghada, Hamila, Syrine, Triki, Sawsen, Ataoui, Asmaou, Keita, Rihab, Ben Othman, Houda, Ghardallou, Rahma, Karmous, Mouad, El Bardi, Chiraz, Lassoued, Lilia, Laadhar, Yassine, Khadhar, Fatma, Aouini, Melek, Ben Mrad, Nabil, Ben Romdhane, Sana, Hamdi, Sarra, Chenik, Yassine, Jabloun, Amira, Talhaoui, Houaida, Mahfoudhi, Mariem, Ghardallou, Aymen, Noamen, Haythem, Raddaoui, Chedia, Chourabi, Amani, Amorri, Houssem, Boukhili, Ahlem, Khannouch, Molka, Louati, Hassan, Alzain, Achref, Hamdani, Sabrine, Bousnina, Zeineb, Ajra, Refaat, Gheni, Riadh, Ben Hmida, Taha, Ounissi, Zied, Ibn Elhadj, Wafa, Fekih, Maha, Ben Yedder, Wafa, Medi, Jamel, Elghoul, Afef, Ben Dayekh, Bechir, Ben Radhia, Khawla, Nasser, Haifa, Mtir, Chokri, Kortas, Imene, Mgarrech, Marah, Jamli, Hela, Kaddour, Nouha, Mekki, Imene, Amamou, Assil, Achour, Sami, Ouannes, Sameh, Ben Farhat, Abdelaziz, Jaouadi, Saeb, Ben Saad, and Rim, Letaief

Subjects
Cardiovascular Diseases, Cardiology, Humans
Published
2022

5. Thromboembolic complications in children with primary nephrotic syndrome: A Tunisian series

Author

Abir, Boussetta, Chaker, Jaber, Manel, Jellouli, and Tahar, Gargah

Subjects
Male, Venous Thrombosis, Nephrotic Syndrome, Child, Preschool, Thromboembolism, Humans, Infant, Female, Thrombosis, Child, Pulmonary Embolism, Retrospective Studies
Abstract

Nephrotic syndrome is a common pathology in children. Despite its good prognosis, it can become complicated and threaten the patient's vital and functional prognosis. Thromboembolic complications are rare but serious.To study the main thromboembolic events and their outcome during primary nephrotic syndrome in children.It was a retrospective study of the records of children followed for primary nephrotic syndrome who presented one or more thromboembolic events.Twenty thromboembolic events in 19 children were identified (15 boys and 4 girls). The average age was 5.13±3.4 years at the time of NS diagnosis. The location of the thrombosis was venous in 14 cases. Cerebral venous thrombosis was noted in seven cases, pulmonary thromboembolism in five cases. We noted deep venous thrombosis of lower limbs in three cases, occlusive mesenteric ischemia in two cases, vein portal thrombosis in one case, renal vein thrombosis in one case, and thrombosis of a peripheral artery in one case.Venous and arterial thrombotic complications can occur in children with nephrotic syndrome. Clinical features may be subtle; therefore, neuroimaging and angiographic techniques are essential for diagnosis.

Published
2022

9. Primary heterotopic pleural hydatidosis: a rare entity

Author

Amira Dridi, Sarra Zairi, Chaker Jaber, Hazem Zribi, Imen Bouassida, Adel Marghli, Rime Essid, Henda Neji, and Mahdi Abdennadher

Subjects
medicine.medical_specialty, Primary (chemistry), business.industry, medicine, Rare entity, Radiology, business
Published
2021
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