Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Sameh Ellouze"'
Autor:
Saloua Krichen Makni, Chiraz Chaari, Sameh Ellouze, Lobna Ayadi, Slim Charfi, Karima Abbes, Mohamed Haj Slimen, Mohamed Nabil Mhiri, Tahia Sallami Boudaoura
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 22, Iss 2, Pp 335-338 (2011)
Mucinous tubular and spindle cell carcinomas (MTSCC) are low-grade renal epi-thelial neoplasms with approximately 100 documented cases reported in the literature. We report a case of MTSCC in a 79-year-old patient in association with a renal tubercul
Externí odkaz:
https://doaj.org/article/305f2e8ba6e9467fbe627992c0152cdb
Autor:
Slim Charfi, Rim Kallel, Hela Mnif, Sameh Ellouze, Mohamed Dhouib, Mohamed Guermazi, Abdelmajid Khabir, Tahya Sellami-Boudawara
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2012 (2012)
Mullerian adenosarcoma of the cervix is a rare tumor composed of benign epithelial and malignant stromal components. Sarcomatous overgrowth and heterologous elements in cervical adenosarcoma are extremely infrequent. We report the case of a 26-year-o
Externí odkaz:
https://doaj.org/article/c8f33776c3134b9a8e4a47bc74836b3e
Autor:
Slim Charfi, Sameh Ellouze, Hela Mnif, Ali Amouri, Abdelmajid Khabir, Tahya Sellami-Boudawara
Publikováno v:
Case Reports in Pathology, Vol 2012 (2012)
Plasmacytoid variant of melanoma is reported in only rare cases. We present the case of a 54-years-old man admitted for enlarged lymph nodes in the lumbar region. Initial diagnosis of plasmablastic lymphoma/plasma cell myeloma was considered. At our
Externí odkaz:
https://doaj.org/article/a2ced75e48be4b5e9910fb514f8946f7
Autor:
Chiraz Ben Ayed, J. Feki, Slim Charfi, Tahya Boudawara-Sellami, Kais Chaabane, Sameh Ellouze, Jamel Daoud, Mounir Frikha, Hela Mnif
Publikováno v:
Breast Disease. 34:87-93
BACKGROUND: Mammary neuroendocrine carcinoma (NEC) displays morphological features including mucinous type. OBJECTIVE: To describe clinicopathological of NEC with mucinous differentiation. METHODS: A total of 15 cases of mammary NEC with mucinous dif
Autor:
Ibtissem Bahri, Moez Elloumi, Hatem Bellaaj, Mohamed Guermazi, Tahya Boudawara, Naourez Gouiaa, Hanen Abid, Sameh Ellouze, Saloua Makni, Doulira Louati, Hela Mnif
Publikováno v:
Imagerie de la Femme. 21:111-114
Resume Le plasmocytome est une tumeur maligne qui derive des plasmocytes ; sa localisation ovarienne est exceptionnelle ; nous rapportons un cas de plasmocytome ovarien bilateral diagnostique en postoperatoire ; il n’y avait pas de gammapathie mono
Autor:
Nabil Tahri, Raja Mokdad-Gargouri, Imen Miladi-Abdennadher, Mounir Frikha, Lobna Ayadi, Sameh Ellouze, Ali Amouri, Abdelmajid Khabir, Tahia Sellami-Boudawara
Publikováno v:
Familial Cancer. 10:567-571
Familial adenomatous polyposis (FAP) is an autosomal dominant disorder which typically presents with colorectal cancer in early adult life, secondary to extensive adenomatous polyps of the colon. In addition to the colonic manifestations, the syndrom
Autor:
Tahya Boudawara, Slim Charfi, Chiraz Chaari, Sameh Ellouze, Naourez Gouiaa, Abdelkhalek Hssini, Mariem Kessentini, Ibticem Bahri Zouari
Publikováno v:
Annales de Pathologie. 31:98-101
Uterine leiomyoma with massive lymphoid infiltration is a rare and unusual pathological finding; only 20 cases have been reported in the literature. We report a case of this unusual lesion in a 35-year-old woman who underwent a myomectomy. On gross e
Autor:
Saloua Makni, Ahmed Guirat, Sameh Ellouze, Chiraz Chaari, Tahya Boudawara, Doulira Louati, L. Mnif
Publikováno v:
Imagerie de la Femme. 20:44-47
Resume L’œdeme massif de l’ovaire (OMO) est une condition pseudotumorale benigne et rare, survenant chez des femmes jeunes, pouvant mimer une tumeur ovarienne. Les auteurs rapportent sept cas d’OMO dans le but de rappeler les principales carac
Autor:
Tahya Boudawara, Sameh Ellouze, H. Fakhfekh, S. Krichen-Makni, L. Ayadi, C. Châari, M. N. Mhiri, M. Frikha, N. Toumi
Publikováno v:
Oncologie. 11:53-57
Introduction Le carcinome a` petites cellules (CPC) de la vessie est une tumeur rare repre-sentant 0,5 % de l’ensemble des tumeurs vesicales, elle est hautement agressive. Elle est caracterise e par un potentiel metastatique tres important. Sa pris
Autor:
Sameh Ellouze, B. Ben Ayed, T. Sallemi Boudawara, Afef Khanfir, Rim Kallel, S. Krichen Makni, S. Chaabouni, Imen Chtourou, Mohamed Guermazi
Publikováno v:
Oncologie. 10:563-567
Les tumeurs a cellules de la granulosa juvenile de l’ovaire sont des tumeurs rares qui representent moins de 5 % des tumeurs ovariennes de l’enfant et de l’adolescent, la majorite de ces tumeurs sont diagnostiquees au stade I (FIGO) avec un pro