Zobrazeno 1 - 10
of 154
pro vyhledávání: '"Nazik, Allali"'
Autor:
Chaymae Faraj, MD, Khadija Laasri, MD, Sara Essetti, MD, Yahya El Harras, MD, Nazik Allali, PhD, Siham El Haddad, PhD, Latifa Chat, PhD, Loubna Aqqaoui, PhD, Sarah Hosni, PhD, Fouad Ettayebi, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4526-4530 (2024)
Hydatidosis is a parasitic disease caused by the tapeworm Echinococcus. Echinococcus Granulosus is the most common cause of hydatid disease in humans. Bone involvement is rare, accounting for only 0.9% to 2.5% of all cases. We report the case of an 8
Externí odkaz:
https://doaj.org/article/123821e7154f48778fdf70fb4b119045
Autor:
Sara Essetti, Chaymae Faraj, Fatima Chait, Sara Ez-Zaky, Nazik Allali, Siham El Haddad, Latifa Chat
Publikováno v:
Radiology Case Reports, Vol 19, Iss 9, Pp 3878-3881 (2024)
Septo-optic dysplasia (SOD) is a rare congenital condition characterized by a triad of septum pellucidum dysgenesis, optic nerve hypoplasia, and hypothalamic-hypophyseal dysfunction. In some cases, additional brain anomalies such as schizencephaly ca
Externí odkaz:
https://doaj.org/article/173671a5062d4132ac4fe16f6f07cca4
Autor:
Yousra Guelzim, Ismail Halfi Mohamed, Salma Marrakchi, Soumia Krioule, Salma Tahri, Mounia El Yousfi, Fatima El Hassouni, Rachid Maakoul, Nazik Allali, Latifa Chat, Siham El Haddad
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3478-3482 (2024)
Conjoined twins occur in an estimated one in every 200,000 live births. The etiology remains largely speculative, with genetic and environmental factors being considered. The thoraco-omphalopagus type accounts for approximately 40% of cases, making i
Externí odkaz:
https://doaj.org/article/220da0fa8be648e1b9a4811159c0df21
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:
Salma Marrakchi, MD, Ouiam Taibi, MD, Sara Ez-zaky, MD, Moustaine El Mamoune, MD, Bouanane Rania, MD, Nazik Allali, PhD, Latifa Chat, PhD, Siham El Haddad, PhD
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 47-50 (2025)
Hydatidosis, caused by the larval form of the parasite Echinococcus granulosus, is a rare condition, especially in pediatric patients, with pleural involvement being exceedingly uncommon. We report a case of primary pleural hydatidosis in a 9-year-ol
Externí odkaz:
https://doaj.org/article/634c32a95f0442f48203198dc59b5333
Autor:
Jihane El Houssni, Sanae Jellal, Ismail Neftah, Fariss Dehayni, Siham El Haddad, Nazik Allali, Latifa Chat
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 69-74 (2025)
The Polysplenia Syndrome (PSS) is a form of heterotaxy, a rare congenital anomaly with an estimated incidence of 1 in 250,000 live births, first described by Helwig in 1929. Most patients with polysplenia syndrome die during the neonatal period due t
Externí odkaz:
https://doaj.org/article/026cb0cd47ee4a04b3d4b267b37f7f97
Autor:
Sara Ez-zaky, MD, Salma Marrakchi, MD, Sara Essetti, MD, Sanae Jellal, MD, Najat Lamalmi, PhD, Nazik Allali, PhD, Latifa Chat, PhD, Siham El Haddad, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 5872-5876 (2024)
Yolk sac tumors can occur in various extragonadal sites, including the hepatobiliary tract, and are often associated with elevated serum alpha-fetoprotein. We report the case of a 14-month-old male infant presenting with abdominal pain and distension
Externí odkaz:
https://doaj.org/article/e6238fd6425641ef94d4cd3705eea5b9
Autor:
Fatima Zohra Benbrahim, MD, Lina Belkouchi, MD, Nazik Allali, PhD, Siham El Haddad, PhD, Latifa Chat, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5191-5195 (2024)
Susac syndrome is a rare microangiopathy of unclear etiology, likely autoimmune, characterized by a characteristic clinical triad of encephalopathy, retinopathy, and hypoacusis. The majority of cases reported in the literature involve adult patients,
Externí odkaz:
https://doaj.org/article/078f552f107a4a5c967ae1254605be51
Autor:
Yousra Guelzim, Abdallah Bennasser, Salma Marrakchi, Abdelkader Sqalli Houssaini, Salwa Idoubba, Ismail Boujida, Ahmed Jahid, Nazik Allali, Latifa Chat, Siham El Haddad
Publikováno v:
Radiology Case Reports, Vol 19, Iss 7, Pp 2585-2589 (2024)
Demons-Meigs syndrome is a very rare entity. It combines a benign ovarian “fibroma-like” tumor with ascites and hydrothorax. The notion of benignancy is the key point. CA-125 levels are most of the time normal, but high levels can be observed in
Externí odkaz:
https://doaj.org/article/3f8586145373458d8f427a79ab4ba8b9
Autor:
Nourrelhouda Bahlouli, Yahya El Harras, Fatima Chait, Khadija Laasri, Nazik Allali, Latifa Chat, Siham El Haddad
Publikováno v:
Radiology Case Reports, Vol 19, Iss 6, Pp 2545-2548 (2024)
Nephroblastoma or Wilms' tumor is the most common malignant tumor of the kidney in the pediatric population. Metastasis is caused by hematogenous spread. The most common localizations in decreasing order of frequency are lymph nodes, lungs, and liver
Externí odkaz:
https://doaj.org/article/308edd0c8b9647f6ae0a22389bac5fdc