Zobrazeno 1 - 10
of 136
pro vyhledávání: '"Siham El haddad"'
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:
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:
Ihssan Hadj Hsain, Chehrastane Rachida, Lahlou Chaimae, Marrakchi Salma, Boutaleb Joud, Nadia Cherradi, Hafsa El ouazzani, Nazik Allali, Latifa chat, Siham EL haddad
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 863-866 (2025)
This review presents the case of a 9-year-old patient who reported headaches and unilateral nasal obstruction, without fever, and with a generally preserved condition. An endoscopic examination revealed a polypoid fleshy mass in the left nasal cavity
Externí odkaz:
https://doaj.org/article/85308e9a4eb248b18ab9938333095a37
Autor:
Fatima Zohra Benbrahim, MD, Siham EL Haddad, PhD, Lina Belkouchi, PhD, Chaymae Faraj, MD, Sanae Jellal, MD, Joud Boutaleb, MD, Nazik Allali, PhD, Latifa Chat, PhD
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 550-555 (2025)
Nephroblastoma tumor is the most common renal tumor in children aged 1 to 5 years, typically presenting as an abdominal mass. However, other nonspecific signs may also reveal the disease. An unusual presentation, such as acute pyelonephritis or a sub
Externí odkaz:
https://doaj.org/article/06748e68309447c8ad81610c119347ff
Autor:
Chaimae Lahlou, MD, Chaymae Faraj, MD, Sara Essetti, MD, Ihssan Hadj Hsain, MD, Nazik Allali, PhD, Siham EL Haddad, PhD, Latifa Chat, PhD
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 509-514 (2025)
Pediatric neuro-meningeal tuberculosis leads to high rates of mortality and morbidity. Prompt diagnosis and initiation of treatment are challenging; imaging findings play a key role in establishing the presumptive diagnosis. General brain imaging fin
Externí odkaz:
https://doaj.org/article/138bed80a62c4e9ba48b03efdde8212d
Autor:
Jihane El Houssni, Sanae Jellal, Fariss Dehayni, Ismail Neftah, Siham El Haddad, Nazik Allali, Latifa Chat
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 256-260 (2025)
Fibrodysplasia ossificans progressiva is a rare and severely debilitating genetic disorder affecting approximately 1 in 2 million people. It is characterized by progressive heterotopic ossification of soft tissues, leading to the formation of ectopic
Externí odkaz:
https://doaj.org/article/0f9093819a0b41a5980a8fd06f775403
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