Background: Testicular microlithiasis is a rare, usually asymptomatic, non-progressive disease of the testes associated with various genetic anomalies, infertility and testicular tumors. According to our literature search, ...

A malignant soft tissue hemangiopericytoma metastatic to the thoracic wall in a 65 year old man is reported. Although the MRI of both the primary and metastatic foci revealed complementary finding of a network of ...

Introduction: When the disease is in rare localization and especially has not a typical appearance of hydatid cyst, incorrect definitive diagnosis may be defined mistakenly, since the disease may be easily missed unless ...

En-plaque tuberculoma is a rare manifestation of CNS tuberculosis and presents as a solitary, focal, caseous plaque-like lesion. It is difficult to differentiate en-plaque like meningeal tuberculoma from true primary ...

The decision to implant vena cava filters, either temporary or permanent, is difficult in young patients. We present the case of a young man with pulmonary embolism in whom temporary and permanent inferior vena cava filters ...

Objective. To evaluate hemodynamic changes in mesenteric arteries in patients with Behçet disease with and without gastrointestinal symptoms. Methods. Doppler sonography of mesenteric arteries was performed in 25 symptomatic ...

Subacute sclerosing panencephalitis (SSPE) is a rare, progressive, inflammatory neurodegenerative disease. Our aim was to determine the metabolic abnormalities of brain in early- and late-stage SSPE by using MR spectroscopy ...

Sandhoff’s disease is a rare, genetic lysosomal storage disease leading to delayed myelination or demyelination. Although neuroimaging findings in this disease have been reported previously, magnetic resonance spectroscopy ...

Giant axonal neuropathy (GAN) is a rare genetic disease of childhood involving the central and peripheral nervous systems. Axonal loss with several giant axons filled with neurofilaments is the main histopathological feature ...

Korpus kallozum disgenezisinin değişik formları ile eşlik eden beyin anomalileri ve klinik bulgular arasındaki ilişkinin araştırılması. GEREÇ VE YÖNTEM Kallozal disgenezisli 169 olgunun MRG bulguları retrospektif olarak ...