Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Ahmed Jahid"'
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:
Hamza Sekkat, Jihane El Hamzaoui, Kouassi Serge Kouamé Armel, Jaouad Naddouri, Ahmed Jahid, Ihssan Elouarith, Youness El Bakali, Mohammed Raiss, Farid Sabbah, Abdelmalek Hrora, Mouna Mhamdi El Alaoui
Publikováno v:
Journal of Minimal Access Surgery, Vol 20, Iss 2, Pp 229-232 (2024)
Benign cystic mesothelioma is a very rare and uncommon lesion, first reported by Plaut in 1928. It affects young women of reproductive age. It is usually asymptomatic or has non-specific symptoms. Diagnosis remains difficult despite the evolution of
Externí odkaz:
https://doaj.org/article/18422a1bec7a49cfbd1c35b6cc6f58b9
Autor:
Ibtissam Elouali, Kawtar Imrani, Kenza Berrada, Hiba Zahi, Ahmed Jahid, Nabil Moatassim Billah, Ittimade Nassar
Publikováno v:
SAGE Open Medical Case Reports, Vol 11 (2023)
Mucosal melanoma is a rare subtype of melanoma distinct from the cutaneous type in its clinical and biological aspects, requiring different therapeutical management. Anorectal melanomas represent less than 1% of anorectal cancers and 0.3% of malignan
Externí odkaz:
https://doaj.org/article/419a8b077d5741658daa7ecf760bf18d
Autor:
Yasmine Laraqui Houssein, Sabrine Derqaoui, Raissouni Khouloud, Ahmed Jahid, Fouad Zouaidia, Zakiya Bernoussi, Kaoutar Znati
Publikováno v:
Clinical Pathology, Vol 15 (2022)
Hepatoid adenocarcinoma is a rare type of extrahepatic adenocarcinoma with glandular and hepatocyte differenciation. The tumor can occur in many organs, generally in the stomach, the location of the lung being extremely rare. Despite poor prognosis a
Externí odkaz:
https://doaj.org/article/60ff01c34f854ba187e47098c97307c9
Publikováno v:
Case Reports in Pathology, Vol 2021 (2021)
Primary leiomyosarcomas (LMS) of vascular origin are rare tumors, and more than half of the cases arise in the inferior vena cava (IVC). Primary LMS of the renal vein are extremely rare tumors with only a few cases reported in the literature. Their d
Externí odkaz:
https://doaj.org/article/b673c3f3efcb45beb51e5dd0816ee622
Publikováno v:
Case Reports in Urology, Vol 2021 (2021)
Synchronous renal cell carcinomas (RCC) and angiomyolipomas (AML) occurring in the same kidney are rare. Cases in the setting of tuberous sclerosis (TS) have been reported in the literature. However, the association of these tumors in the same kidney
Externí odkaz:
https://doaj.org/article/263a7838d587433c946ce9328ca4ef5f
Autor:
Mustapha Azzakhmam, Fouad Zouaidia, Ahmed Jahid, Kaoutar Znati, Zakia Bernoussi, Najat Mahassini
Publikováno v:
The Pan African Medical Journal, Vol 30, Iss 225 (2018)
Le pseudo myxome péritonéal (PMP), est un syndrome clinicopathologique caractérisé par une ascite mucineuse et des pools de mucine comportant un épithélium mucineux néoplasique dans la cavité péritonéale. Le PMP est peu fréquent, et se pr
Externí odkaz:
https://doaj.org/article/69e214a5938f4bb0966464877cda0cf6
Autor:
Youness Jabbour, Youssef Jabri, Hamza Lamchahab, Mohammed Tbouda, Ahmed Jahid, Tarik Karmouni, Khalid El Khader, Abdellatif Koutani, Ahmed Iben Attya Andaloussi
Publikováno v:
Case Reports in Urology, Vol 2018 (2018)
Lymphoepithelioma-like carcinoma of the bladder (LELCB) is a rare variant of urothelial carcinoma first described by Zukerberg in 1991 and confirmed as a variant of urothelial carcinoma by the WHO classification of tumors of the urinary system. LELCB
Externí odkaz:
https://doaj.org/article/7d226e6c76474b80a598b0fc63942ef0
Autor:
Mustapha Azzakhmam, Fouad Zouaidia, Ahmed Jahid, Zakia Bernoussi, Kaoutar Znati, Asmae Lakhdissi, Mohamed Bouchikh, Najat Mahassini
Publikováno v:
The Pan African Medical Journal, Vol 28, Iss 198 (2017)
Le blastome pulmonaire décrit surtout chez les enfants, est une tumeur rare. Elle représente 0.25 à 0.5% de toutes les tumeurs pulmonaires avec un pronostic très grave. Sur le plan histologique, il s'agit d'une tumeur à double composante: une co
Externí odkaz:
https://doaj.org/article/b30aa0eac28e49ce94089e974a190742
Autor:
Habiba Kadiri, Ahmed Jahid, Fouad Zouaidia, Yassir Sbitti, Nabil Ismaili, Hassan Errihani, Zakia Bernoussi, Najat Mahassini
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 49, Iss 3, Pp 373-376 (2010)
Externí odkaz:
https://doaj.org/article/bc5557bbbe9c4ed7a38520dae3a8b00f