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30 results on '"Sabiri, Mouna"'

6. Eccrine porocarcinoma: an extremely rare cutaneous tumor from a radiological point of view – case report and review of the literature

Author

Mahdar, Imane, primary, Lembarki, Ghizlane, additional, Jamil, Jihad, additional, Safi-eddine, Hiba, additional, Najib, Belmoudden, additional, Sabiri, Mouna, additional, Labied, Mohamed, additional, El Manjra, Samia, additional, Samira, Lezar, additional, Diouri, Mounia, additional, and Essodegui, Fatiha, additional

Published
2022
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7. Hémangiome hépatique: le light bulb sign

Author

Jadib, Abdelhamid, primary, Labied, Mohamed, additional, Daki, Anouar, additional, Lembarki, Ghizlane, additional, Sabiri, Mouna, additional, El Manjra, Samia, additional, Lezar, Samira, additional, and Essodegui, Fatiha, additional

Published
2022
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10. Le signe de la double ligne dans l’ostéonécrose

Author

El Ouazzani, Lamiaa Chahidi, primary, Haboussi, Mohamed Reda, additional, El Moudden, Hanane, additional, Labied, Mohamed, additional, Lembarki, Ghizlane, additional, Sabiri, Mouna, additional, lezar, Samira, additional, and Essodegui, Fatiha, additional

Published
2022
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11. Le signe du bonhomme de neige

Author

Boumlik, Keltoum, primary, Bentaleb, Daoud, additional, Adyel, Rim, additional, Lembarki, Ghizlane, additional, Labied, Mohamed, additional, Sabiri, Mouna, additional, Lezar, Samira, additional, and Essodegui, Fatiha, additional

Published
2022
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19. Leiomyoma of the Inferior Vena Cava

Author

Abakar, Djidda, primary, Aghrib, Fatiha, additional, Beddi, Amina, additional, Sabiri, Mouna, additional, manjra, Samia El, additional, Lezar, Samira, additional, and Essodegui, Fatiha, additional

Published
2021
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20. Zinner Syndrome

Author

Djidda, Abakar, additional, Badi, Fatima-Ezzahrae, additional, Sabiri, Mouna, additional, Elmanjra, Samia, additional, Lezar, Samira, additional, and Essodegui, Fatiha, additional

Published
2021
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27. Tumoral calcinosis of unusual location in a chronic hemodialysis patient.

Author

Sakhy Y, Taoussi R, Ndayishimiye V, Sabiri M, Labied M, Lembarki G, El Manjra S, Lezar S, and Essodegui F

Abstract

Tumoral calcinosis is a rare cause of intratissular calcifications in hemodialysis patients with chronic renal failure. Its frequency is estimated between 0.5 and 7% of patients. We illustrate through a case of unusual localization diagnosed in Ibn Rochd University Hospital, Casablanca, Morocco, the radiographic and scannographic aspect of this little known entity. A 40-year-old man, followed for hypertensive cardiopathy, in chronic renal failure for 12 years under hemodialysis, consulted for bilateral inguinal swellings evolving in a progressive and painless way. Biological investigations revealed hyperparathyroidism with increased phosphocalcic product. He was referred to us for radiological evaluation which revealed lesions in favor of bilateral puboinguinal tumor calcinosis. Tumoral calcinosis is a rare cause of intratissular calcifications in chronic renal failure patients undergoing hemodialysis. Pubic localization with infiltration and osteolysis of the symphysis pubis is very rare. Its main risk factors are the existence of hyperparathyroidism, an increase in phosphocalcic product and probably local traumatic factors. Tumoral calcinosis has a typical appearance on radiographs: amorphous, cystic and multilobulated calcifications of periarticular distribution. The CT scan allows a better delineation of the calcified mass. Its treatment remains controversial. The knowledge of osteoarticular manifestations of chronic hemodialysis patients, especially tumoral calcinosis by radiologists, allows to easily make the diagnosis and thus avoid invasive complementary explorations for the patient and to quickly institute an effective treatment., (© 2023 The Authors. Published by the British Institute of Radiology.)

Published
2023
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28. Eccrine porocarcinoma: an extremely rare cutaneous tumor from a radiological point of view - case report and review of the literature.

Author

Mahdar I, Lembarki G, Jamil J, Safi-Eddine H, Najib B, Sabiri M, Labied M, El Manjra S, Samira L, Diouri M, and Essodegui F

Abstract

Eccrine porocarcinoma is a rare type of skin neoplasm. It represents less than 0.01% of all epithelial cutaneous tumors. Early diagnosis is the only way to minimize the mortality rate, given its aggressive nature and the high rate of local recurrence and metastasis. Clinical diagnosis is challenging and the confirmation is histological. Few studies have been published about the radiological features of eccrine porocarcinoma. We report a case of a localized eccrine porocarcinoma along with ultrasound, MRI features, and a review of the literature to highlight the role of imaging in the diagnosis and treatment plan., (© 2022 The Authors. Published by the British Institute of Radiology.)

Published
2022
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29. [Leriche syndrome in a 20-year-old young woman: a case report].

Author

Noureddine L, Bentaleb D, Boumlik K, Sabiri M, Lembarki G, Lezar S, Elmanjra S, and Essodegui F

Subjects
Aorta, Abdominal surgery, Echocardiography, Doppler methods, Female, Humans, Iliac Artery diagnostic imaging, Iliac Artery surgery, Ischemia diagnostic imaging, Leriche Syndrome surgery, Lower Extremity blood supply, Young Adult, Aorta, Abdominal diagnostic imaging, Leriche Syndrome diagnostic imaging, Thrombosis diagnostic imaging
Abstract

Leriche syndrome or aortoiliac occlusive disease is a particular obliterative arterial disease of the lower limbs, consisting of thrombotic occlusion of the aortoiliac junction. We here report the case of a 20-year-old female patient with no particular past medical history, presenting with acute lower limb ischemia. Lower extremity echo Doppler showed overall decrease in arterial blood flow without visualization of endoluminal material. Lower limb angioscaner showed arterial thrombosis of the abdominal aorta extended to bilateral external iliac arteries. The patient subsequently underwent aortic-bi-iliac bypass surgery with good evolution as well as assessments for possible thrombogenic mechanism., Competing Interests: Les auteurs ne déclarent aucun conflit d´intérêts., (Copyright: Leila Noureddine et al.)

Published
2021
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30. Zinner Syndrome.

Author

Abakar D, Badi FE, Sabiri M, El Manjra S, Lezar S, and Essodegui F

Abstract

Zinner syndrome is a developmental anomaly of the urogenital tract. This condition is defined by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. The syndrome is due to malformation of the mesonephric duct during embryogenesis. The condition used to be rare but is now frequently encountered due to the advent of MRI and CT. MRI confirms the diagnosis by revealing the seminal vesicle cyst and its contents, and the ejaculatory duct obstruction, while CT confirms renal agenesis. We report the case of a young patient with Zinner syndrome., Learning Points: Zinner syndrome consists of the triad of renal agenesis, seminal vesicle cyst and ejaculatory duct obstruction.Any insult during embryogenesis of the mesonephric duct in men can result in Zinner syndrome.Pelvic MRI is the gold standard to confirm the diagnosis of Zinner syndrome., Competing Interests: Conflicts of Interests: The authors declare there are no competing interests., (© EFIM 2021.)

Published
2021
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