Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Fatima Chait, MD"'
Autor:
Fatima Chait, MD, Nourrelhouda Bahlouli, MD, Chaymae Faraj, MD, Sara Essetti, MD, Nidal Mrani Alaoui, PhD, Narjiss Alami, MD, Bouchra El basri, MD, Naima Erraimi, PhD, Zaitouna Alhamany, PhD, Nazik Allali, PhD, Siham El Haddad, PhD, Latifa Chat, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3400-3404 (2024)
Gastrointestinal duplication is an infrequent congenital disorder characterized by the presence of a muscular layer covered by mucosa. Gastric duplication cysts account for approximately 2%-9% of all gastrointestinal duplication cysts. The typical cl
Externí odkaz:
https://doaj.org/article/aaa306dd8fad4b61ae911c2444cb53c2
Autor:
Chaymae Faraj, MD, Youssef Mahdi, PhD, Sara Essetti, MD, Fatima Chait, MD, Hatim Essaber, MD, Asaad El Bakkari, MD, Youssef Omor, PhD, Rachida Latib, PhD, Sanae Amalik, PhD, Basma El Khannoussi, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 4950-4954 (2024)
Primary hepatic leiomyosarcoma (PHL) is a rare malignant tumor, which originates from smooth muscles. The imaging features are nonspecific and the diagnosis is often delayed until the tumor reaches a large size, which leads often to a dismal prognosi
Externí odkaz:
https://doaj.org/article/adaf89e634894933985e1f28f6c20011
Autor:
Chaymae Faraj, MD, Kaoutar Imrani, PhD, Sara Essetti, MD, Fatima Chait, MD, Chaimae Lahlou, MD, Nabil M. Billah, PhD, Ittimade Nassar, PhD, Amina A. Babana, MD, Youssef O. Touhami, MD, Hadj Omar El Malki, PhD, Lahcen Ifrine, PhD, Abdelkader Belkouchi, PhD, Omar Belkouchi, MD, Rihane El Mohtarim, MD, Sabrine Derqaoui, PhD, Zakiya Bernoussi, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 4945-4949 (2024)
Inflammatory pseudotumor (IP) is a rare type of benign tumor. Although initially identified in the lung, it has now been identified in a number of somatic and visceral sites, but mesenteric presentation is uncommon and has a variable clinical present
Externí odkaz:
https://doaj.org/article/b3912a5fa1464fc2878bd061c0b95a13
Autor:
Khadija Laasri, MD, Amine Naggar, MD, Nourrelhouda Bahlouli, MD, Fatima Chait, MD, Ilyass Ahallat, MD, Moncef Boufettal, PhD, Reda Allah Bassir, PhD, Jalal Mekkaoui, PhD, Mohamed Kharmaz, PhD, Moulay Omar lamrani, PhD, Mohamed Saleh Berrada, PhD, Fouad zouaidia, PhD, Omar El aoufir, PhD, Fatima Zahra Laamrani, PhD, Laila Jroundi, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 9, Pp 3145-3151 (2023)
Hydatid disease is still endemic in several regions worldwide including Morocco, and is caused in most cases by the larval form of 2 species of the tapeworm Echinococcus: E. granulosus and E. multilocularis. Primary hydatid disease of the bone withou
Externí odkaz:
https://doaj.org/article/60c277d8d14c46388bd190c56b3b4e0c
Autor:
Fatima Chait MD, Nourrelhouda Bahlouli MD, Khadija Laasri MD, Kaouthar Sfar MD, Najat Lamalmi PhD, Nazik Allali PhD, Siham El Haddad PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
Burkitt’s lymphoma is rare but highly aggressive and very fast-growing B-cell non-Hodgkin’s lymphoma (NHL). It can affect any organ such as the central nervous system, jaw, intestines, kidneys, ovaries, and other organs. It results from the malig
Externí odkaz:
https://doaj.org/article/6ad6899c1d5648e19c987d41e454721a
Autor:
Fatima Chait MD, Nourrelhouda Bahlouli MD, Rachida Chehrastane MD, Nidal Mrani Alaoui PhD, Fadoua Boughaleb MD, El alami Zouheir PhD, El Medhi Tarik PhD, Nazik Allali PhD, Siham El Haddad PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
Poland syndrome is indeed a rare congenital malformation that can present with various degrees of thoracic and homolateral upper limb anomalies. The classic features of Poland syndrome include agenesis or hypoplasia of the sternocostal head of the pe
Externí odkaz:
https://doaj.org/article/2b22d75eda854fb18353e5c0e6cb7731