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Sponsored AI Networking Cookbook: Practical recipes for AI-assisted network automation and development AI Networking Cookbook: Practical recipes for AI-assisted network automation and development

Author

M. Maaroufi

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4 papers indexed here

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Open access Aug 2026

Aggressive Squamous Cell Carcinoma Arising in Chronic Xanthogranulomatous Pyelonephritis: CT Imaging of a Rare Case with Hepatic Metastases

Xanthogranulomatous pyelonephritis (XGP) is a rare, severe form of chronic renal infection associated with long-standing urinary tract obstruction, most commonly due to staghorn calculi. Although considered a benign inflammatory condition, it may rarely be associated with or evolve into squamous cell carcinoma (SCC) of...

Wiame Bougrine, I. Chaouche, Brahim El Mahjoub et al. · 0 citations
Case report Open access Aug 2026

Incidental discovery of neglected 11β-hydroxylase deficiency causing 46,XX disorder of sex development in a 35-year-old adult: A radiologically driven diagnosis

11β-hydroxylase deficiency (11β-OHD) is the second most common form of congenital adrenal hyperplasia (CAH), characterized by androgen excess, mineralocorticoid-driven hypertension, and hypokalemia. We report a 35-year-old individual with a 46,XX karyotype, registered and raised male since birth, in whom a disorder of...

Salma Abouchiba, N. Ennejjari, H. Ouazzani et al. · 0 citations
Open access Sep 2026

Imaging and etiologic spectrum of cavernous sinus syndrome: a retrospective observational study of 26 patients

Background: Cavernous sinus syndrome (CSS) is a rare but potentially life-threatening condition caused by a heterogeneous group of neoplastic, vascular, and inflammatory lesions. Its diagnosis represents a significant clinical challenge owing to overlapping presentations and the complex anatomy of the cavernous sinus r...

Wiame Bougrine, Brahim El Mahjoub, H. O. Chahdi et al. · 0 citations
Open access Aug 2026

MRI Evaluation of a 46, XX Disorder of Sex Development Due to Classical 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia in a 6-Month-Old Infant: A Case Report

Background: Classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most common cause of 46,XX disorders of sex development (DSD), resulting in androgenic virilization of the female external genitalia. Magnetic resonance imaging (MRI) plays a central and increasingly indispensable role in...

Zaid Ennasery, Salma Abouchiba, Hajar El Ouazzani et al. · 0 citations

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