Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hafsa El Ouazzani"'
Autor:
Hamza Retal, Soumya EL Graini, Hafsa EL Ouazzani, Nadia Cherradi, Meriem Fikri, Najwa Echcherif El Kettani, Mohamed Jiddane, Firdaous Touarsa
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 55, Iss 1, Pp 1-6 (2024)
Abstract Cauda equina syndrome is a surgical emergency caused by the compression of the lumbosacral nerves. The most frequent cause is discal herniation, while tumoral pathology in this region is rare, and congenital processes are less common. We rep
Externí odkaz:
https://doaj.org/article/5477340e9f734425bbb1b04aa8d43748
Autor:
Hajar Zebbakh, MD, Abir Lemrabet, MD, Fatima Zohra Benbrahim, MD, Youssef Omor, PhD, Rachida Latib, PhD, Nadia Cherradi, PhD, Hafsa El Ouazzani, PhD, Sanae Amalik, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3449-3452 (2024)
The primary malignant melanoma of the parotid is a rare and complex clinical entity, posing numerous diagnostic challenges due to the absence of melanin in the tumor and its histological similarities with other poorly differentiated lesions. Accurate
Externí odkaz:
https://doaj.org/article/c8106efcd38a47868ebc6f394d2c54d6
Autor:
Hafsa El Ouazzani, Firdaous Touarsa, Zaynab Iraqui Houssaini, Mahdi Hakkou, Mohammed Yasaad Elouadghiri, Abdessamad Ouhabi, Mohamed Jiddane, Fouad Zouaidia, Nadia Cherradi
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 16 (2023)
Rosai-Dorfman disease (RDD) is a clonal histiocytic proliferation characterized by large S100 positive histiocytes with variable emperipolesis. Extranodal locations were confirmed with the central nervous system or the meninges involvement in less th
Externí odkaz:
https://doaj.org/article/a534707b4cdf4097bad5f24ee10401d1
Autor:
Fatima Zahra Mrabet, Hafsa El Ouazzani, Leila El Akkari, Sanaa Hammi, Jamal Eddine Bourkadi, Fouad Zouaidia
Publikováno v:
Case Reports in Pulmonology, Vol 2018 (2018)
Primary pleuropulmonary synovial sarcoma is extremely rare. The diagnosis can only be made after having eliminated an extrapleuropulmonary localization in the past and at the time of diagnosis. Our presentation is about a 40-year-old woman having a c
Externí odkaz:
https://doaj.org/article/770c7a8e899e4858a3ecc590e943562e
Autor:
Youness Jabbour, Hamza Lamchahab, Sumba Harrison, Hafsa El Ouazzani, Tarik Karmouni, Khalid El Khader, Abdellatif Koutani, Ahmed Iben Attya Andaloussi
Publikováno v:
Case Reports in Urology, Vol 2018 (2018)
Xanthogranulomatous prostatitis is a rare benign inflammatory process of the prostate. Only few cases have been reported in the English literature. Xanthogranulomatous prostatitis is usually an incidental finding after needle biopsy or transurethral
Externí odkaz:
https://doaj.org/article/e6ef494935f84704b1d20a1065b2adaa
Autor:
Hafsa El Ouazzani, Imane Azzam, Zainab Benyahya, Rachida Chehrastane, Abdelilah Oujilal, Fouad Zouaidia, Nadia Cherradi
Publikováno v:
Journal of Surgical Case Reports. 2023
Infantile myofibromatosis (IM) is the most common fibrous disorder of infancy and early childhood. Solitary intracranial involvement is rare and often unrecognized. This makes its early diagnosis and adequate management difficult. The majority of les
Publikováno v:
International Journal of Surgery Case Reports. 107:108175
Autor:
Hafsa El Ouazzani, Hamza Lamchahab, Tarik Karmouni, Khalid El Khader, A. Koutani, Ahmed Iben Attya Andaloussi, Youness Jabbour, Sumba Harrison
Publikováno v:
Case Reports in Urology, Vol 2018 (2018)
Xanthogranulomatous prostatitis is a rare benign inflammatory process of the prostate. Only few cases have been reported in the English literature. Xanthogranulomatous prostatitis is usually an incidental finding after needle biopsy or transurethral
Autor:
Jamal Eddine Bourkadi, Leila El Akkari, Fouad Zouaidia, Sanaa Hammi, Hafsa El Ouazzani, F.Z. Mrabet
Publikováno v:
Case Reports in Pulmonology, Vol 2018 (2018)
Case Reports in Pulmonology
Case Reports in Pulmonology
Primary pleuropulmonary synovial sarcoma is extremely rare. The diagnosis can only be made after having eliminated an extrapleuropulmonary localization in the past and at the time of diagnosis. Our presentation is about a 40-year-old woman having a c