Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Ezzeddine, Abderrahim"'
Autor:
Meriam Hajji, Salah Saied, Ikram Mami, Yassine Khadhar, Tasnim Ben Ayed, Imen Gorsane, Fethi Ben Hamida, Jalel Ziadi, Mohamed Karim Zouaghi, Ezzeddine Abderrahim
Publikováno v:
Case Reports in Nephrology, Vol 2024 (2024)
Introduction. Longer survival in dialysis led to a higher incidence of vascular access complications and failure. With the limited access to kidney transplantation programs and peritoneal dialysis, exhaustion of vascular access for hemodialysis is an
Externí odkaz:
https://doaj.org/article/29fa803f98294aeeb5d194998e90eab5
Autor:
Hajji Meriam, Hayet Kaaroud, Rahma Karray, Fethi Ben Hamida, Kahena Bouzid, Ezzeddine Abderrahim
Publikováno v:
Case Reports in Nephrology, Vol 2024 (2024)
Background. Urinary lithiasis constitutes a recurrent pathology affecting a relatively young population. The risk of progression to chronic renal failure and the cost of treatment are the most important issues. Primary hyperparathyroidism (PHPT) is r
Externí odkaz:
https://doaj.org/article/937528062be3494ba7956c60e5eb61a0
Autor:
Meriam Hajji, Imen Gorsane, Samaraa Badrouchi, Noureddine Litaiem, Soumaya Rammeh, Fethi Ben Hamida, Ezzeddine Abderrahim
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-4 (2023)
Abstract Background Lupus nephritis and lupus erythematosus tumidus (LET) are uncommon manifestations of systemic lupus erythematosus (SLE), and their coexistence as the initial presentation of SLE is exceedingly rare. Here, we report such a case, em
Externí odkaz:
https://doaj.org/article/1b28bcdd96c84130ac36db5e9c7bb7d5
Autor:
Meriam Hajji, Samia Barbouch, Hayet Kaaroud, Khaoula Ben Abdelghani, Fethi Ben Hamida, Amel Harzallah, Ezzeddine Abderrahim
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 16 (2023)
Introduction: Hemophagocytic lymphohistiocytosis (HLH) is a disease of multi-organ dysfunction due to excessive immune activation causing widespread inflammation and tissue destruction. It is a severe condition associated with high morbidity and mort
Externí odkaz:
https://doaj.org/article/81f9dba5694146a08eff0923fe5d5acb
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 16 (2023)
Dent’s disease is a rare genetic kidney disorder characterized by proximal tubular dysfunction, nephrocalcinosis, recurrent nephrolithiasis, and chronic kidney disease. Hypercalcemia is a rare finding in this disease. In this report, we present a c
Externí odkaz:
https://doaj.org/article/6393aba1c53c4a599e3f5d6ad7641698
Publikováno v:
Clinical Case Reports, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Multiple myeloma (MM) results from malignant plasma cell disorder. It represents approximately 10% of hematological malignancies and it is typically diagnosed in the elderly with a median age of 70 years and has a steep increase in incidence
Externí odkaz:
https://doaj.org/article/6cd02af503564e8d98622a489f2ade9d
Autor:
Hajji Meriam, Asma Bettaieb, Hayet Kaaroud, Fethi Ben Hamida, Taher Gargeh, Ridha Mrad, Kahena Bouzid, Ezzeddine Abderrahim
Publikováno v:
International Journal of Nephrology, Vol 2023 (2023)
Introduction. Primary hyperoxaluria type 1 (PH1) is a rare and inherited condition of urolithiasis. The aim of our study was to analyze clinical, paraclinical, and evolutionary aspects of PH1 in adult patients in our Nephrology department. Methods. W
Externí odkaz:
https://doaj.org/article/18c3e0db8544427081d5656a45b72f24
Autor:
Asma Kefi, Khaoula Ben Abdelghani, Ilef Ben Jemaa, Mounira Elleuch, Cyrine Sassi, Myriam Jrad, Sami Turki, Ezzeddine Abderrahim
Publikováno v:
Clinical Case Reports, Vol 11, Iss 1, Pp n/a-n/a (2023)
Abstract Tuberculous tenosynovitis of the hand is a very rare condition. Herein, we report the case of tuberculous tenosynovitis of the hand in a 32‐year‐old woman. We highlight the success of anti tuberculosis drugs alone without resort to surgi
Externí odkaz:
https://doaj.org/article/faf0477cccf14988a0f6b311be9e0aa2
Autor:
Soumaya Chargui, Rawnak Houli, Mondher Ounissi, Fethi Ben Hamida, Amel Harzallah, Ezzeddine Abderrahim
Publikováno v:
Clinical Case Reports, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Among salt‐wasting tubulopathies' complications, venous thrombosis is one of the rarest. We report a case of a young woman with Gitelman syndrome (GS). She presented a deep venous thrombosis in her leg and was treated with heparin with fav
Externí odkaz:
https://doaj.org/article/e74d4d354ed043d48abc6605e3d2fe76
Autor:
Hayet Kaaroud, Amel Harzallah, Mariem Hajji, Soumaya Chargui, Samia Barbouch, Sami Turki, Raja Trabelsi, Rim Goucha, Fatma Ben Moussa, Hedi Ben Maiz, Fethi Ben Hamida, Ezzeddine Abderrahim
Publikováno v:
International Journal of Nephrology, Vol 2022 (2022)
Background. Renal amyloidosis is one of the main differential diagnoses of nephrotic proteinuria in adults and the elderly. The aim of this study with the most important series in our country is to contribute to the epidemiological, clinical, and eti
Externí odkaz:
https://doaj.org/article/b5467d3fb425405186a314dbb80dedbc