Zobrazeno 1 - 10
of 169
pro vyhledávání: '"Akammar A"'
Autor:
Amina Hamdaoui, Assia Benchekroun, Kaoutar Maasaoui, Hicham Elbtioui, Amal Akammar, Nizar El Bouardi, Mariam Haloua, Moulay Youssef Lamrani, Mariam Boubbou, Mustapha Maaroufi, Badr Alami
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5527-5530 (2024)
A 46-year-old farmer living in a rural area, who sustained an injury to his left foot 10 years ago, consulted due to progressive swelling of the same foot. An MRI revealed the “dot-in-circle” sign, suggestive of mycetoma of the foot, also known a
Externí odkaz:
https://doaj.org/article/c783943f926e4be0942e8d7b061de6b2
Autor:
Ghita Lahnine, Fatima Saddouki, Zineb Bouanani, Amal Akammar, Nizar El Bouardi, Meriem Haloua, Badr Alami, Youssef A. Lamrani, Mustapha Maaroufi, Meriem Boubbou
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5196-5200 (2024)
A rare disorder called congenital infiltrating lipomatosis of the face is characterized by a diffuse fatty infiltration of the soft tissues of the face. Muscle involvement and related bony hyperplasia may coexist. This particular form of lipomatous t
Externí odkaz:
https://doaj.org/article/e32174e97d8040ffabd6377d7ba35dec
Autor:
Asmae Rais, Nizar El Bouardi, Zined Bouanani, Amal Akammar, Meriem Haloua, Badreddine Alami, Moulay Youssf Alaoui Lamrani, Meryem Boubbou, Mustapha Maaroufi
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 4747-4750 (2024)
The case presented illustrates a very rare chronic granulomatous disease called the Madura foot or also called mycetoma. It is a chronic granulomatous disease, caused by a contained infection that penetrates the subcutaneous tissues and spreads to th
Externí odkaz:
https://doaj.org/article/b39d1217479a4d0784aa6f40a810e66a
Autor:
Kaoutar Maasaoui, MD, Nizar El Bouardi, MD, Amina Hamdaoui, MD, Amal Akammar, MD, Meryem Haloua, MD, Badreeddine Alami, MD, Moulay Youssef Alaoui Lamrani, MD, Meryem Boubbou, MD, Mustapha Maaroufi, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 4788-4793 (2024)
Central nervous system (CNS) tuberculosis is a postprimary form of tuberculosis with high mortality and morbidity rates, even with early diagnosis and treatment. Focal tuberculous cerebritis is extremely rare, typically occurring in patients without
Externí odkaz:
https://doaj.org/article/a87b2db6ada148668a32d7ba05849713
Autor:
Fatima Saddouki, MD, Fatima Oussi, MD, Insaf Rhalem, MD, Nizar El Bouardi, MD, Amal Akammar, MD, Meryem Haloua, MD, My Youssef Alaoui Lamrani, MD, Meryem Boubbou, MD, Mustapha Maaroufi, MD, Badr Alami, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4631-4635 (2024)
Pilonidal sinus disease is a frequent and recurrent pathology in young adults, with a male predominance, while malignant transformation of the pilonidal sinus is a rare complication, it occurs in 0.1% of patients, with a poor prognosis. Early surgica
Externí odkaz:
https://doaj.org/article/a5df6165e5884274a532b7ed56c74b48
Autor:
Asmae Sekkat, Ismail Chaouche, Ghita Alami Bassim, Amal Akammar, Nizar El Bouardi, Meriem Haloua, Moulay Youssef Alaoui Lamrani, Meryem Boubbou, Mustapha Maaroufi, Badreddine Alami
Publikováno v:
Radiology Case Reports, Vol 19, Iss 9, Pp 3752-3756 (2024)
Exostosis, or osteochondroma, represents the most prevalent primary benign bone tumor, often viewed as a developmental anomaly rather than a true neoplasm. This article presents 2 cases illustrating complications associated with tibial osteochondroma
Externí odkaz:
https://doaj.org/article/e7793bc385954f809e60568f9e4b9ad4
Autor:
Zineb Bouanani, Insaf Rhalem, Ghita Lahnine, Amal Akammar, Nizar El Bouardi, Badreddine Alami, Youssef Alaoui Lamrani, Mustapha Maaroufi, Meryem Boubbou
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4569-4571 (2024)
Complete cerebellar agenesis is an extremely rare condition characterized by the complete absence of cerebellar tissue. Only a small number of cases have been reported, with varying motor and cognitive deficits. We describe a case of an 11-month-old
Externí odkaz:
https://doaj.org/article/24aececadb274711b251bd9dba642c9c
Autor:
F. Oussi, G. Lahnine, Y. Abdourabbih, A. Akammar, N. El Bouardi, B. Alami, M. Boubbou, M. Maaroufi, M.Y. Alaoui Lamrani
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 5958-5962 (2024)
Peribiliary cysts are an incidental finding in patients with advanced liver disease. They were found to be common in fibrocystic disorders such as autosomal dominant polycystic kidney disease and polycystic liver disease, as well as cirrhotic livers.
Externí odkaz:
https://doaj.org/article/ddbd7f26615e4d4c872122385762dbd8
Autor:
Zineb Bouanani, Asmae Raïs, Fatima Zahra Benbrahim, Amal Akammar, Nizar El Bouardi, Meryem Haloua, Youssef My Alaoui Lamrani, Meryem Boubbou, Mounia Serraj, Bouchra Amara, Marouane Lakranbi, Yassine Ouadnouni, Mohammed Smahi, Mustapha Maaroufi, Badreddine Alami
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3473-3477 (2024)
Most of the pulmonary endobronchial lesions are malignant in origin. In rare instances, benign lesions such as endobronchial hamartoma may be the cause of the endobronchial tree obstruction. We present the case of a 57-year-old male patient from Nort
Externí odkaz:
https://doaj.org/article/dd95058c0ad6479b9c09a4ba90ddc35b
Autor:
Ghita Lahnine, Btissam Benabderrazik, Amal Akammar, Nizar El Bouardi, Badreddine Alami, Moulay Y.A. Lamrani, Mustapha Maaroufi, Meryem Boubbou, Meriem Haloua
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3434-3438 (2024)
Ovarian dysgerminoma is a rare germ cell tumor accounting for 1%-2% of all malignant ovarian tumors and is generally associated with a good prognosis. The condition is more frequent in young women and can arise in dysgenetic gonads that contain gonad
Externí odkaz:
https://doaj.org/article/d466d124f6134246b516862bb68dee7d