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Open access Sep 2026

Imaging-based diagnosis of late-onset tuberous sclerosis complex presenting with acute renal hemorrhage

Tuberous sclerosis complex (TSC) is a rare multisystem genetic disorder characterized by hamartomatous lesions affecting multiple organs, most commonly the brain, kidneys, skin, heart, and lungs. Although typically diagnosed in childhood, late-onset presentations may occur, particularly when renal manifestations predom...

Kawtar Khaissidi, I. Chaouche, H. Ouazzani et al. · 0 citations
Review Open access Sep 2026

HYDATID DISEASE: SPECTRUM OF ATYPICAL LOCATIONS AND COMPLICATIONS ON IMAGING. A PICTORIAL REVIEW

Hydatid disease, or cystic echinococcosis, is a parasitic zoonosis caused by the larval stage of Echinococcus granulosus and remains endemic in Morocco. Although the liver and lungs account for most cases, the parasite may lodge in any organ or soft tissue, where it mimics a wide range of benign and malignant lesions....

M. El Mekhtoume, Ennejjari Nahla, Moulayemin Beddy et al. · 0 citations
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
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

MRI is a valuable, non-irradiating modality for the comprehensive evaluation of internal genitourinary anatomy in 46,XX DSD secondary to CAH, providing essential information for sex assignment, surgical planning, and multidisciplinary management decisions.

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

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