Zobrazeno 1 - 10
of 24
pro vyhledávání: '"khaled bouzaidi"'
Autor:
Moufida Mahmoudi, Ghada Gharbi, Amal Khsiba, Amine Jallouli, Asma Ben Mohamed, Manel Yakoubi, Mouna Medhioub, Lamine Hamzaoui, Khaled Bouzaidi, Mohamed Mousadek Azouz
Publikováno v:
Future Science OA, Vol 9, Iss 9 (2023)
Aim: Ruptures of the intra-abdominal vein causing a spontaneous hemoperitoneum in cirrhotic patients is a rare condition. However, diagnosis must be considered early in cirrhotic patients with hematic ascites as a delayed diagnosis with hemodynamic i
Externí odkaz:
https://doaj.org/article/ca2b79f354aa4510aa0a361d9f26cc55
Autor:
Manel Moalla, Amal Khsiba, Moufida Mahmoudi, Khaled Bouzaidi, Emna Chelbi, Asma Ben Mohamed, Manel Yakoubi, Mouna Medhioub, Lamine Hamzaoui, Mohamed Moussadek Azzouz
Publikováno v:
Future Science OA, Vol 9, Iss 4 (2023)
Usually, fatty hepatic infiltration is diffuse and homogeneous. However, in some cases, it can be localized simulating benign or malignant tumors. We present a case of a 61-year-old female patient with family history of malignancy: sister with lung c
Externí odkaz:
https://doaj.org/article/22e84dc79aeb42fe9d7f9628123be8b5
Autor:
Ahmed Ben Salem, Siwar Sbaihi, Hazem Beji, Slim Zribi, Mohamed Saifeddine Mahmoud, Khaled Bouzaidi
Publikováno v:
IDCases, Vol 31, Iss , Pp e01716- (2023)
Externí odkaz:
https://doaj.org/article/54957089e63a4dd4bd893d4e1807d330
Publikováno v:
International Journal of Mycobacteriology, Vol 9, Iss 3, Pp 316-318 (2020)
The association of pulmonary tuberculosis and Behçet's disease revealed by an aneurysm of the humeral artery is exceptional with a complicated management. We report a case in which the two conditions occurred concomitantly with the vascular complica
Externí odkaz:
https://doaj.org/article/0aad81c9a9da4062aeaa8dee1a2d2af8
Publikováno v:
International Journal of Mycobacteriology, Vol 4, Iss 2, Pp 161-164 (2015)
The tuberculosis of the hand and the wrist is a rare entity. Affecting the scapholunate joint is exceptional. It is usually diagnosed at an advanced stage of carpal destruction, due to slowly development of the symptoms. We report the case of a 58-ye
Externí odkaz:
https://doaj.org/article/16ac3ad6e63e44b786b9741287364444
Publikováno v:
The Pan African Medical Journal, Vol 19, Iss 200 (2014)
L'atteinte du muscle strié au cours de la tuberculose chez un sujet immunodéprimé ou à partir de l'extension d'un foyer ostéo-articulaire de voisinage est rare mais bien connue. Toutefois, l'atteinte primitive est exceptionnelle ainsi que celle
Externí odkaz:
https://doaj.org/article/08f3a1080326476ea544947c83ad4df9
Autor:
Mahdi Bouassida, Mohamed Mongi Mighri, Khaled Trigui, Mohamed Fadhel Chtourou, Selim Sassi, Bilel Feidi, Fathi Chebbi, Khaled Bouzaidi, Hassen Touinsi, Sadok Sassi
Publikováno v:
The Pan African Medical Journal, Vol 15, Iss 9 (2013)
Meckel's diverticulum is the most common congenital malformation of the gastrointestinal tract. It can cause complications in the form of ulceration, hemorrhage, intussusception, intestinal obstruction, perforation and, very rarely, vesicodiverticula
Externí odkaz:
https://doaj.org/article/2677dabb814d4155b69b1be84d548b58
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 1, Pp 121-121 (2016)
Dermatofibrosarcoma protuberans is a rare cutaneous mesenchymal tumor characterized by a low potential of malignancy with a very low rate of metastasis but an important rate of local recurrence. Its transformation into a fibrosarcoma is exceptional,
Externí odkaz:
https://doaj.org/article/c3abc5ed8a9c4a16bad6fb0b59856479
Autor:
amal khsiba, manel moalla, Moufida Mahmoudi, khaled bouzaidi, Asma Ben Mohamed, Manel Yakoubi, Mouna Medhioub, Lamine Hamzaoui, Mohamed Msaddak Azzouz
We present a case of a 61-years old female patient with family history of malignancy who presented with multiple nodules at the ultrasonography images. CT scan and MRI were not sufficient to pose a certain diagnosis which was later confirmed by liver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::342b7c8b04f02a2d365fcb4d714166d2
https://doi.org/10.22541/au.165511477.71211000/v1
https://doi.org/10.22541/au.165511477.71211000/v1
Publikováno v:
La Tunisie medicale. 99(4)
Yellow nail syndrome is a very rare disorder. The classic clinical presentation includes a triad involving yellow nail discoloration, chronic pulmonary manifestations and lower limb lymphedema. Its etiology remains unknown and the genetic disorder is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::38173dd7d21539716901f156fdfd70d4
https://pubmed.ncbi.nlm.nih.gov/35244933
https://pubmed.ncbi.nlm.nih.gov/35244933