Skip to content
M

Manel Loukil

Publications (4)

Hydatid Cyst of the Calf: A Rare Location of Hydatid Disease

Raja Amri, Mohamed Othmen Chouchène, Romdhane Denguezli, Manel Loukil, Khaled Bouzaidi & Mohamed Ali Sbai · Asian Journal of Orthopaedic Research · 2020

The location of the hydatid cyst in the soft tissues is exceptional. The localization in the leg produces a swamped painful leg which poses a diagnostic problem, particularly with thrombophlebitis of the lower limb. Ultrasound and Doppler Ultrasound allow the differential diagnos...

Open access Research Article

Longitudinal Transverse Myelitis with Locked in Syndrome Revealing a Systemic Lupus Erythematosus

Raja Amri, Mohamed Othmen Chouchène, Boutheina Ben Ammou, Manel Loukil & Mohamed Ali Sbai · Asian Journal of Research and Reports in Neurology · 2020

The neuropsychiatric manifestations of lupus are very heterogeneous and are a source of significant morbidity and mortality. Transverse myelitis is a rare but serious complication of systemic lupus erythematosus, classically described as an acute attack with a poor functional pro...

Open access Research Article

Butane Poisoning Complicated by Severe Rhabdomyolysis and Compartment Syndrome: A Case Report

Romdhane Denguezli, Raja Amri, Wafa Garbouj, Boutheina Ben Ammou, Manel Loukil & Mohamed Ali Sbai · Asian Journal of Orthopaedic Research · 2020

Carbon Monoxide poisoning remains the leading cause of toxic morbidity and mortality in the world. It remains a public health problem. The occurrence of compartment syndrome and rhabdomyolysis is an exceptional complication but can worsen the prognosis of this intoxication. Compa...

Open access Research Article

Congenital Agenesia of the Inferior Vena Cava: A Diagnosis to Mention in Front of a Deep Vein Thrombosis

Raja Amri, Romdhane Denguezli, Wafa Garbouj, Khaled Bouzaidi, Manel Loukil & Mohamed Ali Sbai · Asian Journal of Case Reports in Medicine and Health · 2020

Congenital agenesia of the inferior vena cava (IVC) is an extremely rare morphological anomaly in the general population; found in approximately 0.0005% to 1% [1]. It is a rare cause of deep vein thrombosis (DVT) and could be responsible for less than 5% of thromboses without a c...

Open access Research Article