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Biomedical subjects

C J Davis

Publications and source records attributed to C J Davis.

At least 91 records · Page 5Linked to original sources

Multilocular cystic nephroma: a radiographic-pathologic correlation of 58 patients.

Clinical radiographic, and pathologic findings of multilocular cystic nephroma (MLCN) in 58 patients are presented. The lesion that affects predominantly boys in childhood and women in adulthood is usually solitary but rarely can be multiple, and it commonly occurs as an asymptomatic mass, occasionally with hematuria. Tumors may grow slowly over years or rapidly within months. A mass that is usually identified on plain radiographs occasionally has curvilinear calcification. Excretory urography and retrograde pyelography are helpful when pelvic herniation of the tumor is recognized, or when septae are noted with total body opacification. Angiography showed an avascular mass (six lesions), a hypovascular mass (14 lesions), or a hypervascular mass three lesions). Ultrasonography is helpful when multiple circumscribed sonolucent areas are identified. Similarly, a multilocular mass with septae is usually identified by computed tomography (six of seven cases). Our findings and a review of the literature indicate that this lesion is a neoplasm that can be strongly suspected preoperatively if pelvic herniation or a multilocular pattern is noted on imaging studies.

Adolescent↗

The radiology of juxtaglomerular tumors.

Nine cases of proven juxtaglomerular tumor of the kidney are reviewed. Each patient presented with hypertension; elevated peripheral renin levels were found in four patients. As in past studies, this tumor occurred more frequently in women (7/9 cases). Although the patients tended to be younger (mean age, 31 years) than those with essential hypertension, all but two patients were more than 20 years of age. In all cases, the tumor was solitary, well-defined, and curable by surgery. The tumor was identified by excretory urography in 5/8 patients who underwent this procedure. A solid renal mass was detected in each of the seven patients examined by ultrasound. Since the tumor tends to be isodense with normal renal parenchyma, it is sometimes not seen on computed tomography without intravenous contrast material. Arteriography revealed a hypovascular mass in each of the nine patients. The combination of a hypovascular solid renal mass in a patient with elevated renin but no renal artery lesions should suggest the diagnosis of a juxtaglomerular cell tumor.

Adolescent↗

Air-flow limitation in myasthenia gravis. The effect of acetylcholinesterase inhibitor therapy on air-flow limitation.

In a survey of 21 patients with myasthenia gravis receiving regular acetylcholinesterase inhibitor therapy, 8 were found to have air-flow limitation associated with their antimyasthenic therapy. In 6 of these subjects, detailed assessments were made of the effect of antimyasthenic therapy on airways function. Pyridostigmine was given together with either placebo or the anticholinergic bronchodilator ipratropium bromide (72 micrograms) by inhalation administered double blind on 2 consecutive days. Airways resistance (Raw) increased significantly after pyridostigmine and placebo inhaler (0.49 +/- 0.13 kPa/L/s basal versus 0.60 +/- 0.13 kPa/L/s at 2 h; mean +/- SEM, p less than 0.05), whereas a significant decrease in Raw followed the combination of pyridostigmine with ipratropium bromide (0.57 +/- 0.08 kPa/L/s basal versus 0.41 +/- 0.07 kPa/L/s at 2 h, p less than 0.05). Thus, acetylcholinesterase inhibitor therapy in subjects with myasthenia gravis with airflow limitation led to significant increase in airways resistance that could be completely reversed by the inhalation of the muscarinic receptor blocker ipratropium bromide.

Airway Resistance↗

Primary malignant renal tumors in the second decade of life: Wilms tumor versus renal cell carcinoma.

Primary renal malignancies occur least frequently in the second decade of life. Of the 4,798 cases of renal cell carcinoma and Wilms tumor referred to the Armed Forces Institute of Pathology 53 renal cell carcinomas and 56 Wilms tumors occurred in the 10 to 20-year age group. Pathologically, both tumors in this age range are similar to those occurring at a more typical age, and histologic differentiation between renal cell carcinoma and Wilms tumor is seldom a problem. While radiographic evaluation is useful to characterize the neoplasm, evaluate the contralateral kidney and detect the presence of tumor extension, current imaging techniques cannot confidently distinguish these 2 tumors.

Adenocarcinoma↗

Angiomyolipoma: ultrasonic-pathologic correlation.

Previous reports of angiomyolipoma have emphasized the ultrasonic finding of a very echogenic intrarenal mass. Ten cases of angiomyolipoma for which ultrasound examinations were available were retrospectively reviewed and correlated with their pathologic findings, and, when available, with computed tomographic findings to determine if other sonographic patterns could be recognized. In addition to the typical echodense pattern (six cases), a mixed pattern (two cases) and a low sonodense pattern (two cases) were discovered. To determine if the typical echodense pattern is specific for angiomyolipoma, 42 cases of renal cell carcinoma for which ultrasound examinations were available were also retrospectively reviewed. In two cases of renal cell carcinoma echodense patterns that were indistinguishable from those of angiomyolipoma were found. Two conclusions are reached: (a) there is a spectrum of ultrasonic findings with angiomyolipoma, and (b) the presence of an echodense intrarenal mass, although very suggestive of angiomyolipoma, is not pathognomonic.

Adenocarcinoma↗

Mesoblastic nephroma: radiologic-pathologic correlation of 20 cases.

The mesoblastic nephroma is a benign renal tumor that usually appears as a neonatal abdominal mass. The tumor is composed of connective tissue that grows between nephrons and usually replaces most of the renal parenchyma. Radiographic and sonographic images reflect this cellular composition and unique growth pattern. The radiographs of 20 cases of mesoblastic nephroma were correlated with their pathologic findings and are described. Urograms usually demonstrate an intrarenal mass two to seven times larger than the contralateral kidney. Contrast medium is occasionally demonstrated within the tumor and may represent function by nephrons trapped within the mesoblastic nephroma. Sonographic studies correlate well with the gross morphology and may be useful in establishing the relation of the tumor to the kidney. Some neovascularity is present on angiographic examination and most tumors are hypervascular. Prognosis after complete excision is excellent and adjunctive therapy is unnecessary.

Adolescent↗

Angiomyolipoma: computed tomographic-pathologic correlation of 17 cases.

The angiomyolipoma is a benign renal tumor composed of fat, smooth muscle, and abnormal blood vessels. The tumor often extends into the perinephric space and often is complicated by intratumoral or perinephric hemorrhage. The CT findings of 17 cases of angiomyolipoma were correlated with their pathologic findings and are described. CT scans usually demonstrate a large fatty mass intermixed with areas of tissue density which may represent nonfatty parts of the tumor or areas of hemorrhage. CT is more sensitive than plain films at detecting the fat within the angiomyolipoma. CT is also useful in identifying perinephric extension and hemorrhage. In those angiomyolipomas composed primarily of smooth muscle or in which intratumoral hemorrhage has obscured the fatty part of the tumor, the CT appearance is indistinguishable from other solid renal tumors.

Adult↗

Capital maintenance and equity erosion in the nursing home industry: a study in one state.

Federal contingencies charge states to regulate the reimbursement of the nursing home industry such that government reimbursement is at a minimal cost that reflects efficient operations, yet at amounts great enough to allow viability and ability to attract and maintain the investment of capital. This study discusses the regulation of the nursing home industry in terms of the significance and costs of financial capital, and the constraints imposed upon states as regulators of capital reimbursement policies. Descriptive financial profiles of nursing homes are provided in one state where the industry alleges inadequacies in the capital reimbursement formula. These financial profiles suggest that the nursing homes investigated have not been able to provide for capital maintenance; instead, the industry may be suffering from equity erosion. Also, the descriptive profiles of capital structure in the nursing home industry differ across three major segments--county, not-for-profit and proprietary homes.

Capital Financing↗

Malignant pheochromocytoma of urinary bladder.

Herein is reported a fifth case of malignant pheochromocytoma of the urinary bladder. Pheochromocytoma represents only 0.4 per cent of bladder tumors with 5 to 10 per cent being malignant. A review of the 4 previously reported cases plus our own suggest that iliac-hypogastric lymphadenectomy should be considered in all cases of pheochromocytoma of the bladder. Early establishment of the malignant potential of these tumors coupled with aggressive surgical treatment improves prognosis.

Humans↗

Renal parenchymal malacoplakia.

Malacoplakia is a rare inflammatory disease which usually involves the bladder and only rarely affects the renal parenchyma. The clinical, radiographic, and pathological findings in 5 cases of renal parenchymal malacoplakia (RPM) are presented and 30 cases from the literature are reviewed. Most patients are middle-aged women with E. coli pyelonephritis. Radiographically, two patterns of involvement are recognized: multifocal and unifocal. The prognosis depends on the pattern and extent of RPM; long-term survival is possible with appropriate therapy.

Adult↗

The neuropathy of abetalipoproteinemia.

The clinical, electrophysiologic, and pathologic features of the peripheral neuropathy in abetalipoproteinemia (Bassen-Kornzweig disease) have been described incompletely. On the basis of findings in threee patients, we believe that large muscle fibers in peripheral nerves are selectively affected and that weakness may be due to chronic partial denervation.

Abetalipoproteinemia↗