Challenge

Challenge





ANSWERS – CASE 159



Hepatitis










Comment


Patients with right upper quadrant pain and abnormal liver function tests are often referred for sonographic evaluation. The main goal in this group of patients is to determine whether there are gallstones and whether there is any evidence of biliary obstruction. In the absence of either of these abnormalities, the next consideration is usually diffuse liver parenchymal disease.


Except for fatty infiltration and, to a lesser degree, cirrhosis, ultrasound is not a good way of evaluating or quantitating diffuse liver disease. Hepatitis is no exception. Nevertheless, there are some sonographic findings that are seen in patients with hepatitis. Perhaps the most common abnormality is thickening of the gallbladder wall (see Case 13). In fact, hepatitis can produce dramatic gallbladder wall thickening. It is also characteristic of patients with hepatitis for the gallbladder lumen to be contracted. Another finding seen commonly is mildly enlarged lymph nodes in the porta hepatis, around the celiac axis, and in the peripancreatic area. Unfortunately, mildly enlarged nodes are very common in these areas and can be associated with many other inflammatory or infectious conditions in the right upper quadrant. They are also common in liver diseases other than hepatitis, such as primary biliary cirrhosis and sclerosing cholangitis.


This case demonstrates the starry sky sign in the liver. Decreased echogenicity of the liver parenchyma around the portal triads and increased echogenicity of the fibrofatty tissues in the triads probably combine to produce this finding. Regardless of the cause, when the portal tracts are imaged in cross section in the periphery of the liver, the net result is small focal areas of increased echogenicity on a darker background, simulating stars in the night sky. Although this finding was described in association with hepatitis, it is not very helpful owing to poor sensitivity and a limited positive predictive value. In addition, when it is present, it is usually subtle enough that diagnostic confidence is limited. The changes seen in this case are considerably more striking than are usually seen.






ANSWERS – CASE 161



Hepatic Focal Nodular Hyperplasia










Comment


Focal nodular hyperplasia (FNH) is a benign tumor of the liver that is composed of Kupffer cells, hepatocytes, and biliary structures. It is hypothesized that it develops from a congenital vascular malformation that promotes hepatocellular hyperplasia. Pathologically, it often has a central, stellate scar. It is supplied by an internal arterial network that is arranged in a spokewheel pattern.


FNH is usually detected as an incidental mass on CT or on ultrasound. Like hepatic adenoma, FNH is more common in women. Unlike hepatic adenoma, it is not related to the use of birth control pills. The nodules seldom bleed or cause any clinical symptoms, although pain may be encountered when the lesions are large.


Although the appearance of FNH varies on sonography, most are isoechoic or nearly isoechoic to liver parenchyma. The central stellate scar, which is frequently seen on contrast-enhanced CT and MRI, is uncommonly seen on ultrasound. However, the spokewheel pattern of internal vascularity is better displayed on color or power Doppler than on CT or MRI.


When FNH is suspected based on ultrasound, sulfur colloid scans can be very useful. Due to the concentration of Kupffer cells, approximately 60% of FNHs are either more intense or isointense to adjacent liver. MRI can also show characteristics findings and is often very helpful. The typical features on ultrasound and either MRI or sulfur colloid scans are sufficient to make the diagnosis with a high degree of certainty. If the lesion is atypical on MRI or sulfur colloid scans, then FNH remains a possibility, but other lesions also need to be considered.



ANSWERS – CASE 162



Biceps Tendon Rupture













ANSWERS – CASE 163



Adrenal Masses










Comment


Ultrasonography is not a primary means of imaging the adrenal glands. Nevertheless, ultrasound frequently identifies masses in the right adrenal gland and infrequently identifies left adrenal gland masses. Right adrenal masses can be imaged from an intercostal or a subcostal approach. Masses appear immediately adjacent to the posterior surface of the liver and lateral to the inferior vena cava. Right adrenal masses are usually superior to the upper pole of the kidney. Left adrenal masses are located in a left paraaortic location at the level of the upper pole of the kidney. They are best identified from a left coronal intercostal approach, using the spleen or kidney as a window, or from an anterior subxiphoid approach.


The most common adrenal mass is the adenoma. Autopsy series identify adenomas in 3% of the population. Adenomas are usually asymptomatic but can produce Cushing’s syndrome (excessive glucocortisol) and Conn’s syndrome (hyperaldosteronism). They contain significant amounts of lipid and are typically low-attenuation lesions on CT. They are usually less than 3 cm in size and homogeneous. Despite their small size, the adrenals are the fourth most common site of metastases. Metastases are usually larger than adenomas and are heterogeneous. Pheochromocytomas produce symptoms of hypertension, headache, tachycardia, anxiety, and palpitations. They are referred to as “the 10% tumor” because 10% are malignant, 10% are extra-adrenal, 10% are bilateral, and 10% occur with MEN syndromes. Pheochromocytomas are typically large, vascular, heterogeneous tumors. Primary adrenal carcinomas are very rare tumors. They are typically very large masses that present with pain or symptoms due to the mass effect. Necrosis, hemorrhage, and calcification are common. Myelolipomas are benign tumors that contain hematopoietic and fatty elements. They rarely cause symptoms and can be small or large.


There is significant overlap in the sonographic appearance of various solid adrenal masses. In most cases, sonographic detection of an adrenal mass is followed by CT or MRI for further characterization. In some instances, laboratory studies are sufficient to determine the etiology of an adrenal mass. In this case, the lesion shown in the first image was a right adrenal metastasis in a patient with lung cancer. The lesion shown in the second image was a left adrenal pheochromocytoma in a hypertensive patient referred for a renal artery Doppler scan. Urinary catecholamine levels documented the diagnosis.






ANSWERS – CASE 165



Full-Thickness Rotator Cuff Tear










Comment


Full-thickness rotator cuff tears are classified as wet or dry, depending on whether there is a significant amount of joint fluid surrounding the torn edges of the cuff. In the patients discussed here, the tears are dry. The appearance of dry tears is somewhat more difficult to understand than wet tears. When the defect created by the tear is not filled with fluid, it must be filled with something else. In most cases, the overlying subdeltoid bursa and peribursal fat drops into the defect. This produces a concavity in the reflections from the bursa and fat. In most cases, this concavity is readily visible at rest. If the torn ends of the tendon have not retracted from each other, a concavity may not be visible at rest. In such a case, compression of the shoulder with the transducer can push the bursa and peribursal fat into the defect at the same time that it produces some separation of the tendon ends. Compression can also exaggerate some tears that are otherwise subtle because they are filled with hypertrophied synovial tissue. This is due to the greater compressibility of the synovium compared to the rotator cuff. The normal rotator cuff does not compress at all.


When there is a massive tear with extensive retraction of the torn tendon, the humeral head becomes completely uncovered by cuff tissue. In such a situation, there is no sonographically visible cuff on standard images. This is referred to as nonvisualization of the cuff. In these cases, the subdeltoid bursa, peribursal fat, and deltoid muscle come into direct contact with the articular cartilage and humeral head.



ANSWERS – CASE 166



Transitional Cell Carcinoma










Comment


Transitional cell cancer (TCC) is typically divided into tumors that involve the bladder and tumors that involve the upper urinary tract (ureter, renal pelvis, and intrarenal collecting system). Bladder tumors are much more common than upper tract tumors, and tumors of the renal pelvis are more common than tumors of the ureter. Approximately 90% of renal pelvis tumors and 99% of ureteral tumors are TCC.


Patients most often present with gross hematuria. Flank pain is uncommon and usually indicates obstruction and hydronephrosis. Colicky pain may develop during periods of clot passage. Patients with advanced disease may present with constitutional symptoms such as weight loss and anorexia.


Sonography is not a primary means of evaluating patients with TCC of the upper urinary tract. However, it may be the first test obtained in a patient with hematuria, and thus the initial identification of the tumor may be with ultrasound. TCC has a variety of sonographic appearances. It may appear as a solid mass within a dilated renal pelvis, as a solid mass distorting the renal sinus fat, or as an area of uroepithelial thickening. In general, the sonographic findings are nonspecific, and the differential diagnosis includes blood clots, sloughed papillae, and pyelonephritis. Detection of internal vascularity confirms that the lesion is viable soft tissue and almost always indicates a tumor of some sort. Further evaluation with intravenous urography, retrograde pyelography, or ureteroscopy is generally required.




Dec 26, 2015 | Posted by in CARDIOVASCULAR IMAGING | Comments Off on Challenge

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