Zobrazeno 1 - 10
of 136
pro vyhledávání: '"M M, Zitouna"'
Autor:
F. Ben Hariz, N. Belkahla, Nadia Maamouri, S. Guellouz, S. Chouaib, Sonia Ketari, N. Ben Mami, I. Chelly-Enneifer, M. M. Zitouna, Hajer Ouerghi
Publikováno v:
La Revue de Médecine Interne. 31:262-267
Resume Introduction La sarcoidose est une maladie granulomateuse d’etiologie indeterminee, caracterisee par la presence de granulomes sans necrose caseeuse et touchant plusieurs organes. L’atteinte gastro-intestinale est rare. L’atteinte gastri
Autor:
J. Kourda, Slim Haouet, K.B. Hammouda, Ines Chelly, M. M. Zitouna, N. Kchir, Amina Mekni, L. Ferchichi, M. Khaldi, Khadija Bellil
Publikováno v:
Neurochirurgie. 54:15-20
Most hemangiopericytomas (HPC) are located in the musculoskeletal system and the skin, while the location in the central nervous system (CNS) is rare. The latter represents 2 to 4% in large series of meningeal tumors, thus accounting for less than 1%
Autor:
K. Ben Hamouda, Emna Braham, I. Bettaieb, N. Kchir, Amina Mekni, Slim Haouet, Selma Bellil, M. M. Zitouna, Khadija Bellil
Publikováno v:
Neurochirurgie. 53:39-42
Chordoid meningioma is an uncommon histopathological variant of meningioma frequently confused with chordoma. Recurrence is not uncommon. The aim of our study is to present the clinical and pathological characteristics of this entity and a review of
Autor:
L. Ferchichi, N. Kchir, M. M. Zitouna, S. Houissa, M. Khaldi, A. Mekni, S. Haouet, Ines Chelly
Publikováno v:
Neurochirurgie. 52:367-370
Resume Les metastases systemiques de glioblastomes cerebraux sont tres rares. Les facteurs de risque favorisant le developpement de ces metastases semblent etre une craniotomie prealable et/ou une longue evolution tumorale. Les localisations systemiq
Publikováno v:
Neurochirurgie. 52:119-122
Autor:
Hajer Ouerghi, I. Chelly-Enneifer, N. Belkahla, M. M. Zitouna, S. Chouaib, N. Ben Mami, Nadia Maamouri, S. Guellouz, F. Ben Hariz, Sonia Ketari
Publikováno v:
Journal Africain d'Hépato-Gastroentérologie. 5:57-59
La lymphangite carcinomateuse (LC) duodenale a ete decrite de facon sporadique. Nous rapportons un nouveau cas de LC duodenale. La fibroscopie œsogastroduodenale objectivait un epaississement des plis de Kerckerning bulbaires dont la surface prenait
Autor:
M, Bel Haj Salah, A, Mekni, K, Nouira, S, Kharrat, K, Bellil, S, Bellil, S, Haouet, I, Chelly, N, Kchir, M M, Zitouna
Publikováno v:
Pathologica. 97(6)
Most of the sinonasal tumours are of epithelial origin. Smooth muscle tumours are extremely rare, they account for less than 2.5% of the mesenchymal neoplasms of the sinonasal tract and the nasopharynx. Fewer than 30 cases of primary leiomyogenic tum
Autor:
I, Chelly, K, Bellil, A, Mekni, S, Bellil, M, Belhadjsalah, N, Kchir, S, Haouet, M M, Zitouna
Publikováno v:
Pathologica. 97(3)
The granular cell tumor is an uncommon tumor that usually appears as a solitary small nodular growth and runs a benign course. It occurs widely throughout the body, but is rarely described in the abdominal wall. The authors report a case of malignant
Autor:
M, Bel Haj Salah, A, Mekni, M, Khanfir, K, Bellil, S, Benhaha-Bellil, I, Chelly, N, Kchir, S, Haouet, M-M, Zitouna
Publikováno v:
Medecine et maladies infectieuses. 36(3)
Visceral leishmaniasis due to Leishmania infantum is endemic in Tunisia. The incidence in adult patients has increased in recent years; but most of these patients are not HIV positive as in other Mediterranean countries where all the cases are associ
Publikováno v:
Pathologica. 96(3)
Peutz-Jeghers syndrome is characterized by multiple polyps throughout the gastrointestinal tract in association with mucocutaneous pigmentation. Although Peutz-Jeghers syndrome polyps are hamartomas, frequent association of this syndrome with both ga