Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Fatimazahra Erregad"'
Autor:
Samia Arifi, Abdelmalek Ousadden, Laila Chbani, Hinde El Fatemi, Layla Tahiri, Ibrahim S. Sidibé, Gabrielle Atsame-Ebang, Khalid Mazaz, Nawal Hammas, Ihsane Mellouki, Fatimazahra Erregad, Boubacar Efared
Publikováno v:
BMC Clinical Pathology, Vol 18, Iss 1, Pp 1-7 (2018)
BMC Clinical Pathology
BMC Clinical Pathology
Background Gastrointestinal stromal tumors (GIST) are the most common primary mesenchymal tumors of the digestive system. The assessment of their biological behavior still remains a scientific challenge. To date, there are no well-established biologi
Autor:
Nawal Hammas, Boubacar Efared, Fatimazahra Erregad, Laila Chbani, Ibrahim S. Sidibé, Hinde El Fatemi
Publikováno v:
Tropical Doctor. 48:238-240
Autor:
Hinde El Fatemi, Nawal Hammas, Fatimazahra Erregad, Boubacar Efared, Ibrahim S. Sidibé, Laila Chbani
Publikováno v:
Gynecologic Oncology Research and Practice
Gynecologic Oncology Research and Practice, Vol 6, Iss 1, Pp 1-7 (2019)
Gynecologic Oncology Research and Practice, Vol 6, Iss 1, Pp 1-7 (2019)
Background Endometrial stromal sarcoma (ESS) is a rare neoplasm accounting for only 0.2% of female genital tract tumors. The primary extra-uterine location of ESS is an extremely uncommon occurrence. Case presentation We present a case of a 64-year-o
Autor:
Boubacar Efared, Ibrahim S. Sidibé, Nawal Hammas, Hinde El Fatemi, Laila Chbani, Fatimazahra Erregad
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Sclerosing angiomatoid nodular transformation of the spleen is a very rare benign vascular lesion recently described. Usually, sclerosing angiomatoid nodular transformation of the spleen is an incidental finding; the association with malig
Autor:
Laila Chbani, Fatimazahra Erregad, Ibrahim S. Sidibé, Gabrielle Atsame Ebang, Boubacar Efared, Nawal Hammas, Layla Tahiri, Moulay Abdelilah Melhouf, Abdelaziz Banani, Hinde El Fatemi
Publikováno v:
Breast disease. 37(3)
BACKGROUND Phyllodes tumors (PT) are uncommon biphasic tumors, accounting for less than 1% of all breast primary neoplasms. They form a wide variety of tumors ranging from benign to malignant. Several histological features are used to grade PT into 3
Autor:
Fatimazahra Erregad, Ibrahim S. Sidibé, Boubacar Efared, Laila Chbani, Hinde El Fatemi, Nawal Hammas
Publikováno v:
Tropical Medicine and Health, Vol 45, Iss 1, Pp 1-3 (2017)
Tropical Medicine and Health
Tropical Medicine and Health
Background Breast tuberculosis is a rare form of extrapulmonary tuberculosis with clinical and radiological misleading presentations. We report herein a retrospective study of clinicopathological features of five cases of breast tuberculosis collecte
Autor:
Ibrahim S. Sidibé, Laila Chbani, Layla Tahiri, Hinde El Fatemi, Gabrielle Atsame-Ebang, Boubacar Efared, Mounia Serraj, Rabiou Sani, Mohamed Smahi, Fatimazahra Erregad, Nawal Hammas
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
Background The occurrence of lung metastasis from benign uterine leiomyomas is rarely reported especially in post menopausal women. The pathogenesis of these metastatic benign tumors still remains a subject of various speculations. Case presentation
Autor:
Boubacar Efared, Gabrielle Atsame Ebang, Laila Chbani, Aboubakry Sow, Hinde El Fatemi, Soufiane Tahirou, Ibrahim S. Sidibé, Fatimazahra Erregad, Moulay Hassan Farih, Nawal Hammas, Layla Tahiri
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 10, Iss 1, Pp 1-5 (2017)
BMC Research Notes, Vol 10, Iss 1, Pp 1-5 (2017)
Background Despite its rich vasculature, the penis is rarely involved by metastasis. Since the first description of penile metastasis in 1870, fewer than 500 cases have been reported in the literature. The pelvic organs are the main source of primary
Autor:
Gabrielle Atsame-Ebang, Nawal Hammas, Abdelmajid El Mrini, Layla Tahiri, Fatimazahra Erregad, Hinde El Fatemi, Laila Chbani, Boubacar Efared, Badarou Chaibou, Asmae Mazti, Ibrahim S. Sidibé
Publikováno v:
BMC Clinical Pathology
BMC Clinical Pathology, Vol 17, Iss 1, Pp 1-5 (2017)
BMC Clinical Pathology, Vol 17, Iss 1, Pp 1-5 (2017)
Background The coexistence of Rosai-Dorfman disease (RDD) with Langerhans cell histiocytosis (LCH) is very rare, as to date only 17 cases have been reported in the english literature. The pathophysiology of this uncommon co-occurrence still remains e