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Biomedical subjects

R J Stanley

Publications and source records attributed to R J Stanley.

At least 55 records · Page 3Linked to original sources
PubMed1988

Hepatic perivascular lymphedema: CT appearance.

The CT appearance of dilated hepatic lymphatics in liver transplant recipients has been described recently. We have observed similar findings of presumed hepatic lymphatic dilatation and perivascular lymphedema in 20 patients seen over an 8-month period, none of whom had received a liver transplant. Review of these patients' records showed that 18 (90%) of 20 had underlying disease processes that could have caused dilated lymphatics as a result of either increased lymph flow or lymphatic obstruction. We have grouped these processes into three etiologic categories: (1) posttraumatic hepatic lymphatic obstruction, (2) obstruction caused by malignant lymphadenopathy, and (3) congestive hepatomegaly caused by cardiac decompensation. The appearance of hepatic lymphatic dilatation and surrounding lymphedema needs to be recognized so that lymphatic dilatation is not mistaken for dilated intrahepatic bile ducts.

Abdominal Injuries↗
PubMed1988

Differentiation between small benign and malignant adrenal masses with dynamic incremented CT.

Contrast-enhanced dynamic incremented CT scans in 37 patients with 44 small adrenal masses (28 benign and 16 malignant) were reviewed by two observers unaware of the histologic diagnosis to determine if applying morphologic criteria could help differentiate small benign adrenal masses from malignant adrenal masses. Only lesions smaller than 5 cm with diagnoses confirmed by histology (12 masses) or follow-up (32 masses) were included. Features evaluated to suggest a benign diagnosis were homogeneous low attenuation, possibly with punctate contrast enhancement; an enlarged gland (adrenal configuration maintained); a thin or absent rim; round or oval shape with sharp margins; and diffusely homogeneous attenuation about equal to or greater than that of muscle. Features studied to suggest a malignant diagnosis were a thick enhancing rim, invasion of adjacent structures, irregular or poorly defined margins, and inhomogeneous attenuation. Both observers' diagnoses of benign vs malignant lesions with CT criteria were highly statistically significant. The positive predictive value of a benign diagnosis was 100% for both observers and of a malignant diagnosis was 82% and 62% for the two observers. Evaluated singly, all but three diagnostic criteria were statistically significant in differentiating lesions for both observers; the other three criteria were present in a smaller percentage of patients, but nevertheless had positive predictive values for benignancy of 89-100%. We conclude that experienced observers who use CT criteria can often discriminate accurately between benign and malignant small adrenal masses and, in particular, minimize the number of false-negative diagnoses of adrenal metastases. If these results are confirmed and refined by prospective studies, aggressive diagnostic evaluation can be eliminated in some patients with benign adrenal lesions.

Adenoma↗
PubMed1988

Idiopathic arterial calcification of infancy with unusual clinical presentations in sisters.

Two cases of idiopathic arterial calcification of infancy that occurred in sisters are reported. One patient died at age 14 months after a protracted course characterized by the nephrotic syndrome, blood chemistry abnormalities, hypertension, seizures, and a microangiopathic hemolytic anemia. Her sister died at age 3 weeks after a precipitous illness that initially was misinterpreted at autopsy as Reye's syndrome.

Calcinosis↗
PubMed1988

Aggressive intranasal carcinoma mimicking infection or inflammation.

In a twenty-year period we have treated five patients with intranasal squamous cell carcinomas who initially were thought to have benign cutaneous disorders of the nasal skin. Advanced squamous cell carcinoma requiring total rhinectomy, often with extensive contiguous midface excision, was found in all patients. Three of these five patients died of their disease. In one patient, a red nose resembling acne rosacea was present. In the four others, chronic cellulitic or ulcerative cutaneous involvement was caused by squamous cell carcinoma. These cases emphasize the need for intranasal examination and appropriate radiologic studies to exclude intranasal carcinoma in patients with apparently unresponsive cutaneous nasal disease.

Adult↗
PubMed1987

Endodermal sinus tumor (yolk sac tumor) of the ear.

Endodermal sinus tumors (yolk sac tumors) are malignant germ cell tumors that usually arise in the gonads. We report what is, to our knowledge, the first known case of an endodermal sinus tumor of the ear. The tumor was present in a developmentally delayed child with an abnormal temporal bone and exhibited histopathologic and immunocytochemical features identical to those of endodermal sinus tumors of gonadal origin. The tumor resolved after chemotherapy, and the patient remained alive without evidence of disease at the time of this writing. The purpose of this report is to add a rare tumor to the differential diagnosis of neoplasms of the ear in children and to familiarize otorhinolaryngologists and head and neck surgeons with its pathologic features and clinical management.

Antineoplastic Combined Chemotherapy Protocols↗
PubMed1987

Calcified adrenal masses.

We reviewed 106 cases of adrenal masses of all types in all age groups. Thirty-three contained calcium visible on radiographs, sonography, or computed tomography (CT). Neuroblastoma was the most common calcified adrenal mass (10 cases), and occurred only in children. Adrenal cyst (6 cases) was the most common calcified adrenal mass in adults. Other calcified adrenal masses included 5 cortical adenomas, 4 adrenal carcinomas, 3 cases of adrenal hemorrhage, 2 adrenal metastases, 2 pheochromocytomas, and 1 histoplasmoma. Calcification within an adrenal mass is therefore nonspecific. All the adrenal cysts had a characteristic radiographic pattern, showing only peripheral curvilinear calcification. The presence and pattern of calcium in an adrenal mass must be correlated with other imaging features (e.g., size, homogeneity, enhancement pattern, margination) to allow correct differential diagnosis. This can best be done by CT.

Adenoma↗
PubMed1987

Malignant hemangiopericytoma: computed tomography and magnetic resonance imaging.

Computed tomography and magnetic resonance imaging of a malignant hemangiopericytoma in a 58-year-old woman are described. The tumor was initially found in the abdomen and resected 34 years ago, but recurred 18 years later, followed by repeated recurrence and eventually metastasis to the lung and then to the liver. The lung nodules were round or oval, homogeneous, and well circumscribed while the massive tumor in the right lobe of the liver was poorly delineated with irregular areas of cystic necrosis. With proper setting of the repetition time and echo delay, the metastatic tumor became distinct from the uninvolved hepatic tissue on magnetic resonance imaging. In this case computed tomography and magnetic resonance imaging were complementary in evaluation of such a tumor.

Abdominal Neoplasms↗
PubMed1986

Oncocytic and oncocytoid carcinoid tumors (well-differentiated neuroendocrine carcinomas) of the larynx.

Carcinoid tumors of the larynx are exceedingly rare neoplasms. With the inclusion of the five neoplasms we report herein, the total number reported in the English-language literature is 16. These five neoplasms all showed light microscopic features of oncocytic (or oncocytoid) cells. Ultrastructurally, all lesions contained dense-core granules of the neurosecretory type. One case further met the ultrastructural criteria for true oncocytoma (that is, an oncocytic carcinoid). The lesion did not metastasize, and the patient was successfully treated surgically. In the other four cases, the lesions were considered to be oncocytoid carcinoids, since they failed to meet the ultrastructural requirements of a true oncocytoma. Each of these four lesions metastasized, although one patient did have a long, indolent course.

Aged↗
PubMed1986

Acute pancreatitis associated with end-stage renal disease.

Various reports in the literature have suggested an association between end-stage renal disease (ESRD) and acute pancreatitis. Little information concerning this association has been discussed in the radiological literature. In this report, the authors review their experience with 54 episodes of acute pancreatitis in 34 patients, including 26 treated with maintenance dialysis, six who underwent renal transplantation, and two managed conservatively before definitive therapy. Ten (29%) of these patients died. Thirty-one computed tomographic (CT) and 49 ultrasound (US) studies of 30 patients were reviewed and demonstrated findings ranging from normal anatomy to fulminant necrotizing pancreatitis. Fifteen US examinations were technically inadequate for evaluation of the pancreas. None of the CT scans were technically inadequate. The authors emphasize the need for increased awareness of ESRD as a possible risk factor for the development of acute pancreatitis.

Acute Disease↗
PubMed1986

Causes of jaundice during hepatic artery infusion chemotherapy.

Jaundice develops in many patients with liver metastases from colorectal adenocarcinoma during hepatic arterial infusion chemotherapy (HAIC). The usual cause is thought to be hepatotoxicity from the chemotherapeutic agent or biliary obstruction from progressive neoplastic disease. The authors evaluated the abdominal computed tomography and ultrasound examinations performed on 49 patients who were jaundiced during long-term HAIC. In only one patient was diffuse intrahepatic biliary dilatation caused by an obstructing mass in the porta. Two patients had metastatic hepatic lesions causing focal biliary obstruction. Intrahepatic dilatation without an obstructing mass occurred in 20 patients. Percutaneous or endoscopic cholangiograms were commonly interpreted prospectively as showing extrinsic compression by metastases, but no mass was confirmed on imaging studies. Seven patients had focal intrahepatic ductal dilatation from stricture without an associated mass. The remaining 19 patients had normal-caliber ducts; their jaundice was caused by chemical hepatitis. This series suggests that the most common causes of jaundice in these patients are chemical hepatitis and common bile duct stricture, complications of intraarterial chemotherapy, rather than neoplastic obstruction. Stricture formation may be confused with extrinsic compression on direct cholangiograms.

Adenocarcinoma↗
PubMed1986

Pain-inducing laryngeal paraganglioma: report of the ninth case and review of the literature.

There are two distinct forms of laryngeal paraganglioma. The patient with the rare Type II has exquisite throat pain that is often clinically confusing. The small size or submucosal location of the lesion often results in a delay in correct diagnosis and treatment. The lesion is very aggressive, even if tiny, generally with widespread metastasis. This tumor should be considered in the differential diagnosis of severe persistent throat pain, especially in the absence of abnormalities on physical or radiologic examination.

Humans↗
PubMed1985

Dense liver in a 72-year-old woman with congestive heart failure.

Amiodarone is a cardiac antiarrhythmic agent now undergoing clinical trials in the United States. Its most important side effect is pulmonary toxicity, which may present radiographically in two forms. One is similar to eosinophilic pneumonia with peripheral alveolar opacities but without any of the laboratory or pathologic findings. A second presentation is as a bilateral interstitial pattern resembling interstitial pulmonary edema. This is often mistaken for heart failure in the clinical and radiographic setting. Amiodarone also causes a phospholipidosis of the liver, which is usually asymptomatic but on occasion may present as hepatitis. On abdominal CT the liver will have an abnormally high attenuation (80-140 HU), which appears to be due to accumulation of an amiodarone metabolite in hepatocytes. This appearance is usually distinguishable from the other causes of increased hepatic attenuation by virtue of other CT criteria and clinical history. However, from a radiographic standpoint alone, the combination of acute congestive heart failure and an abnormally dense liver may result in at least an initial misdiagnosis of advanced primary hemochromatosis.

Aged↗
PubMed1985

Hand-held real-time breast sonography.

The results of real-time hand-held sonographic breast examinations on 86 patients are presented. The technique is described in detail. Sonography was found to be a useful adjunct to the x-ray mammogram in three groups of patients: (1) patients with dense breasts and localized symptomatology or a suspicious area on x-ray mammogram; (2) patients with nonpalpable abnormalities discovered on x-ray mammogram; and (3) patients with palpable masses considered indeterminate on x-ray mammogram. The examination was also found useful for guiding needle aspiration biopsies, in patients with persistent nipple discharge, and in those with breast prostheses. Advantages of the hand-held real-time technique include supine positioning, the ability to flexibly orient the probe, improved resolution due to higher frequency transducers and the lack of compounding, and the ability to vary the amount of compression to assess tissue compliance and fixation. The disadvantage of decreased resolution in the near field can be overcome by attaching a detachable water-path step-off device to the transducer. Geometric distortion from the pressure of the transducer was not believed to be a problem. Hand-held sonographic technique is useful when attention can be directed to a specific area of the breast. The additional information provided results in fewer equivocal interpretations of the x-ray mammogram; however, it should not be used as a substitute for routine mammography.

Adult↗