Ultrasound is used as a primary diagnostic approach to evaluate musculoskeletal disorders and as a guide for treatment. Recently, elastography ultrasound technology has been introduced to complement the limited information conventional ultrasound provides.Elastography is a non-invasive, ultrasound-based technology that evaluates tissue elasticity and stiffness, providing quantitative information on various musculoskeletal disorders. This technology provides more detailed information on conditions such as tendinopathy, muscle injuries, cartilage changes, and soft tissue tumors, contributing to early detection, treatment, and prognosis determination. This review examines the advances in the latest elastography technology and its clinical application cases, evaluating studies on the utility of elastography in musculoskeletal disorders.

BACKGROUND: A toxic dose of bupivacaine produces vasodilation in isolated aortas. The goal of this in vitro study was to investigate the cellular mechanism associated with bupivacaine-induced vasodilation in isolated endotheliumdenuded rat aortas precontracted with phenylephrine. METHODS: Isolated endothelium-denuded rat aortas were suspended for isometric tension recordings. The effects of nifedipine, verapamil, iberiotoxin, 4-aminopyridine, barium chloride, and glibenclamide on bupivacaine concentration-response curves were assessed in endothelium-denuded aortas precontracted with phenylephrine. The effect of phenylephrine and KCl used for precontraction on bupivacaine-induced concentration-response curves was assessed. The effects of verapamil on phenylephrine concentration-response curves were assessed. The effects of bupivacaine on the intracellular calcium concentration ([Ca2+]i) and tension in aortas precontracted with phenylephrine were measured simultaneously with the acetoxymethyl ester of a fura-2-loaded aortic strip. RESULTS: Pretreatment with potassium channel inhibitors had no effect on bupivacaine-induced relaxation in the endothelium-denuded aortas precontracted with phenylephrine, whereas verapamil or nifedipine attenuated bupivacaine-induced relaxation. The magnitude of the bupivacaine-induced relaxation was enhanced in the 100 mM KCl-induced precontracted aortas compared with the phenylephrine-induced precontracted aortas. Verapamil attenuated the phenylephrine-induced contraction. The magnitude of the bupivacaine-induced relaxation was higher than that of the bupivacaine-induced [Ca2+]i decrease in the aortas precontracted with phenylephrine. CONCLUSIONS: Taken together, these results suggest that toxic-dose bupivacaine-induced vasodilation appears to be mediated by decreased calcium sensitization in endothelium-denuded aortas precontracted with phenylephrine. In addition, potassium channel inhibitors had no effect on bupivacaine-induced relaxation. Toxic-dose bupivacaine- induced vasodilation may be partially associated with the inhibitory effect of voltage-operated calcium channels.
4-Aminopyridine ; Animals ; Aorta* ; Barium ; Bupivacaine ; Calcium Channels ; Calcium* ; Glyburide ; Nifedipine ; Phenylephrine* ; Potassium Channels ; Rats* ; Relaxation ; Vasodilation* ; Verapamil

Pancreatic acinar cell carcinoma is an uncommon malignancy of the exocrine pancreas. Because of a higher recurrence rate and frequent metastases, this tumor, generally, has a poor prognosis. We report a case of pancreatic acinar cell carcinoma in a 60-year-old man. His chief complaint was jaundice. Abdominal CT revealed a heterogeneous enhancing mass in the pancreatic head measuring 8.2x7.5cm. After receiving the Whipple procedure, acinar cell carcinoma was diagnosed by pathological examination. Liver metastasis was found at one year after the curative resection.
Acinar Cells ; Carcinoma, Acinar Cell ; Head ; Humans ; Jaundice ; Liver ; Middle Aged ; Neoplasm Metastasis ; Pancreas ; Pancreas, Exocrine ; Prognosis ; Recurrence