Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ihssan Hadj hsain"'
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:
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:
Sara Ez-zaky, MD, Ihssan Hadj Hsain, MD, Sanae Jellal, MD, Sara Essetti, MD, Jamal El Fenni, PhD, Rachida Saouab, PhD, Ouijdane Zamani, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 6582-6586 (2024)
Hemiazygos continuation of a left-sided inferior vena cava (IVC) is an extremely rare developmental anomaly. We present the case of a male patient in whom this condition was incidentally discovered during a thoraco-abdominopelvic CT scan. With the wi
Externí odkaz:
https://doaj.org/article/75ac4b18d2b54c3bbb2630603196f3cb
Autor:
Salma Marrakchi, Ihssan Hadj Hsain, Yousra Guelzim, Najwa El Kettani Ech-Cherif, Meriem Fikri, Mohamed Jiddane, Firdaous Touarsa
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3538-3544 (2024)
Hypertrophic olivary degeneration (HOD) is a rare form of transsynaptic degeneration. It is caused by a damage at the Guillain-Mollaret triangle (GMT), which is defined by three anatomical structures: the dentate nucleus, the red nucleus, and the inf
Externí odkaz:
https://doaj.org/article/da3bcd15184841edb0e93df65cd37041
Autor:
Salma Marrakchi, Khadija Laasri, Rim Moufakkir, Yousra Guelzim, Ihssan Hadj hsain, Zakia El yousfi, Jamal El Fenni, Hassan En-nouali
Publikováno v:
Radiology Case Reports, Vol 19, Iss 6, Pp 2264-2267 (2024)
Palatal tremor has been subdivided into essential (EPT) and symptomatic palatal tremor (SPT). Progressive ataxia and palatal tremor syndrome (PAPT) is a subgroup of symptomatic palatal tremor (SPT). It can be divided into familial and sporadic forms.
Externí odkaz:
https://doaj.org/article/9ee2fc8327f84ceba90a8e47902cbf8a
Autor:
Jihane EL Houssni, MD, Amine Cherraqi, Rachida Chehrastane, Sanae Jellal, Ihssan Hadj Hsain, Siham Oukacem, Nada Adjou, Rachida Saouab, Hassan En nouali, Jamal EL Fenni
Publikováno v:
Radiology Case Reports, Vol 18, Iss 3, Pp 1147-1151 (2023)
Lemmel's syndrome is a rare cause of obstructive jaundice caused by a periampullary duodenal diverticulum compressing the intrapancreatic common bile duct with resultant bile duct dilatation, patients with Lemmel's syndrome usually present with abdom
Externí odkaz:
https://doaj.org/article/99294b7c25814cc1953e13ec72c07d4b
Autor:
Romeo Thierry Yehouenou Tessi, Rita Koudouhonon Oze, Mustapha Outznit, Ihssan Hadj Hsain, Ittimade Nassar, Nabil Moatassim Billah
Publikováno v:
Clinical Case Reports, Vol 11, Iss 1, Pp n/a-n/a (2023)
Abstract Pituitary haemochromatosis is an endocrine disorder caused by the accumulation of iron due to a lack of absorption during haemochromatosis. The characteristic appearance on MRI is a T2 and T2* hyposignal of the anterior pituitary gland witho
Externí odkaz:
https://doaj.org/article/bda131b525ed44f683301e9941ac98c2
Autor:
Romeo Thierry Yehouenou Tessi, Rita Koudouhonon Oze, Mustapha Outznit, Ihssan Hadj Hsain, Ittimade Nassar, Nabil Moatassim Billah
Publikováno v:
Clinical Case Reports. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eb3fe96349cdc8fbeab631772c0aa0f
https://doi.org/10.1002/ccr3.6384
https://doi.org/10.1002/ccr3.6384
Autor:
Salma, Marrakchi, Soumia, El Graini, Ihssan, Hadj Hsain, Nazik, Allali, Latifa, Chat, Siham, El Haddad
Publikováno v:
In Radiology Case Reports December 2024 19(12):6657-6661
Autor:
Salma M; Paediatric Radiology Department, Ibn Sina University Hospital Center, Rabat, Morocco., Salma EA; Paediatric Radiology Department, Ibn Sina University Hospital Center, Rabat, Morocco., Yahya EH; Paediatric Radiology Department, Ibn Sina University Hospital Center, Rabat, Morocco., Samia S; Pathology Department, Ibn Sina University Hospital Center, Rabat, Morocco., Ihssan HH; Paediatric Radiology Department, Ibn Sina University Hospital Center, Rabat, Morocco., Sabrine D; Pathology Department, Ibn Sina University Hospital Center, Rabat, Morocco., Nazik A; Paediatric Radiology Department, Ibn Sina University Hospital Center, Rabat, Morocco., Latifa C; Paediatric Radiology Department, Ibn Sina University Hospital Center, Rabat, Morocco., Siham EH; Paediatric Radiology Department, Ibn Sina University Hospital Center, Rabat, Morocco.
Publikováno v:
Radiology case reports [Radiol Case Rep] 2024 Oct 17; Vol. 20 (1), pp. 140-144. Date of Electronic Publication: 2024 Oct 17 (Print Publication: 2025).