Abnormal brain tumor vasculature has recently been highlighted by a dynamic susceptibility contrast (DSC) MRI processing technique. The technique uses independent component analysis (ICA) to separate arterial and venous perfusion. The overlap of the two, i.e. arterio-venous overlap or AVOL, preferentially occurs in brain tumors and predicts response to anti-angiogenic therapy. The effects of contrast agent leakage on the AVOL biomarker have yet to be established. DSC was acquired during two separate contrast boluses in ten patients undergoing clinical imaging for brain tumor diagnosis. Three components were modeled with ICA, which included the arterial and venous components. The percentage of each component as well as a third component were determined within contrast enhancing tumor and compared. AVOL within enhancing tumor was also compared between doses. The percentage of enhancing tumor classified as not arterial or venous and instead into a third component with contrast agent leakage apparent in the time-series was significantly greater for the first contrast dose compared to the second. The amount of AVOL detected within enhancing tumor was also significantly greater with the second dose compared to the first. Contrast leakage results in large signal variance classified as a separate component by the ICA algorithm. The use of a second dose mitigates the effect and allows measurement of AVOL within enhancement.
The imaging evaluation and interpretation of the triangular fibrocartilage complex (TFCC) is both challenging and rewarding for the radiologist and surgeon alike. The TFCC comprises a complicated group of fibrocartilaginous and ligamentous structures at the ulnar aspect of the wrist that plays an important role in wrist biomechanics. It is the main stabilizer of the distal radioulnar and ulnocarpal joints and functions to distribute compressive forces at the ulnocarpal joint during axial loading. Derangement of the TFCC is the most common source of ulnar-sided wrist pain. Imaging plays an important role in the diagnosis and management of these lesions. The TFCC can anatomically be divided into proximal and distal parts to emphasize the role that the proximal TFCC has in stabilizing the distal radioulnar joint. Tears can be divided into traumatic and degenerative categories using the Palmer classification. Further subclassification based on the location for traumatic tears and the degree of derangement in degenerative tears guides clinical management. The vascular anatomy is important in determining management options for various lesions. A detailed understanding of the normal anatomy of the TFCC, imaging limitations and pitfalls, the Palmer classification system, and current treatment options is critical to the accurate and clinically useful interpretation of radiologic examinations of the TFCC.
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