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Imaging of articular pathology:MRI, CT, arthrography
Berquist, Thomas H.

Clinical Anatomy | August 25, 2002 | Volume: 10 | Issue: 1 | Pages: 1-13

10.1002/(sici)1098-2353(1997)10:1<1::aid-ca1>3.0.co;2-# | PMID 8986381 Get It

Previously undescribed syndrome of spondylometaphyseal dysplasia, osteocartilaginous metaplasia of long bones, and progressive osteolysis of distal phalanges
Osebold, William R., Poznanski, Andrew K., Opitz, John M. , Langer, Leonard O., Spranger, J�rgen W., Unni, K. Krishnan, Spranger, Jürgen W.

American Journal of Medical Genetics | August 25, 2002 | Volume: 80 | Issue: 3 | Pages: 187-195

10.1002/(sici)1096-8628(19981116)80:3<187::aid-ajmg1>3.0.co;2-# | PMID 9843035 Get It

Predicting prostate carcinoma volume and stage at radical prostatectomy by assessing needle biopsy specimens for percent surface area and cores positive for carcinoma, perineural invasion, Gleason score, DNA ploidy and proliferation, and preoperative serum
Sebo, Thomas J., Cheville, John C. , Riehle, Darren, Lohse, Christine M. , Myers, Robert P., Blute, Michael L., Zincke, Horst, Pankratz, V. Shane

Cancer | August 25, 2002 | Volume: 91 | Issue: 11 | Pages: 2196-2204

10.1002/1097-0142(20010601)91:11<2196::aid-cncr1249>3.0.co;2-# | PMID 11391602 Get It

Pulmonary Arteriovenous Fistula: Presentation, Diagnosis, and Treatment
Pick, Adrian, Deschamps, Claude, Stanson, Anthony W.

World Journal of Surgery | August 25, 2002 | Volume: 23 | Issue: 11 | Pages: 1118-1122

10.1007/s002689900634 | PMID 10501873 Get It

Abstract. Pulmonary arteriovenous fistulas (PAVFs) are rare vascular malformations of the lung. There is a strong association with Rendu‐Osler‐Weber disease. Although most patients are asymptomatic, PAVFs can cause dyspnea from a right‐to‐left shunt. They can also bleed and result in hemoptysis and hemothorax. Because of paradoxical emboli, various central nervous system complications have been described including stroke, and brain abscess. Currently, spiral computed tomography offers the most practical method for establishing the presence of PAVFs. Most patients should be treated. Therapeutic options include angiographic embolization with metal coils or balloon occlusion and surgical excision. Angiographic treatment has become the mainstay of therapy for most patients during the last decade. It is less invasive and can be repeated easily. Surgery, which usually consists of a conservative lung resection, is associated with low morbidity and a low recurrence rate. Both therapeutic approaches are discussed. The Mayo Clinic surgical experience of the last 20 years for PAVFs is presented.
Autosomal Genome-Wide Scan for Coronary Artery Calcification Loci in Sibships at High Risk for Hypertension
Lange, Leslie A. , Lange, Ethan M. , Bielak, Lawrence F. , Langefeld, Carl D. , Kardia, Sharon L.R., Royston, Patrick , Sheedy, Patrick F. , Boerwinkle, Eric , Peyser, Patricia A. , Turner, Stephen T.

Arteriosclerosis, Thrombosis, and Vascular Biology | July 28, 2002 | Volume: 22 | Issue: 3 | Pages: 418-423

10.1161/hq0302.105721 | PMID 11884284 Get It

Abstract— Coronary artery disease (CAD) is the leading cause of mortality in the developed world. Although several CAD risk factors, including measures of lipid metabolism, obesity, and blood pressure, have a genetic basis, many genes for CAD susceptibility have yet to be identified. Coronary atherosclerosis is the major cause of CAD, but many with coronary atherosclerosis lack symptoms. Thus, a major limitation of using symptomatic CAD endpoints (eg, sudden coronary death, myocardial infarction) as a study outcome is substantial disease misclassification. Coronary artery calcification (CAC) is part of the atherosclerotic process and is an independent predictor of CAD endpoints. In the present study, CAC was noninvasively quantified by electron beam computed tomography. We performed genome-wide multipoint mode-of-inheritance-free linkage analysis on affected sib pairs, defined as being ≥ the 70th sex- and age-specific percentile for CAC quantity, in a sample of 29 families enriched for hypertension. Almost 95% of participants were asymptomatic for CAD. Our LOD score (log 10 odds in favor of linkage) results provide evidence that chromosomal regions 6p21.3 (maximum LOD score=2.22, P =0.00070) and 10q21.3 (maximum LOD score=3.24, P =0.000057) may harbor genes associated with subclinical coronary atherosclerosis.
Influence of Anatomical Location on Arterial Thrombosis
Karnicki, Krzysztof, Komorowicz, Erzsébet , Fass, David N., Owen, Whyte G., McBane, Robert D. , McBane, Robert

Arteriosclerosis, Thrombosis, and Vascular Biology | July 28, 2002 | Volume: 22 | Issue: 2 | Pages: 342-347

10.1161/hq0202.103999 | PMID 11834539 Get It

Atherosclerosis manifests as a systemic disease with near global involvement of the named segments of the arterial tree. Acute thrombotic arterial occlusion, however, is not equally distributed. To evaluate intra-individual regional differences in arterial thrombogenicity, we compared 111 In-platelet deposition in porcine carotid and femoral arteries after a standardized crush injury. Within the unidirectional flow conditions of elastic carotid arteries, platelet deposition was more than 3-fold higher compared with predominantly muscular femoral arteries with triphasic arterial flow. To determine the influence of rheology on platelet deposition after crush injury, carotid arteries were transplanted into the femoral position and compared with the paired native carotid and femoral arteries. Similarly, femoral arteries transposed to the carotid position were compared with the paired native carotid artery. In each of these experiments, arterial transposition to a new anatomic location imparts a predilection for platelet deposition indigenous to the new location. In the controlled environment of two high-shear thrombin–independent and –dependent flow chambers, porcine carotid and femoral arterial substrates were indistinguishable from one another with respect to platelet deposition. Regional differences in arterial hemodynamics may account for substantial differences in thrombosis arising from deep arterial injury.
Fish-Rich Diet, Leptin, and Body Mass
Winnicki, Mikołaj, Accurso, Valentina, Phillips, Bradley G., Puato, Massimo , Palatini, Paolo , Pauletto, Paolo, Somers, Virend K.

Circulation | July 28, 2002 | Volume: 106 | Issue: 3 | Pages: 289-291

10.1161/01.cir.0000025241.01418.4d | PMID 12119240 Get It

Background — Leptin has been implicated in cardiovascular disease. A diet rich in fish has been associated with decreased cardiac and vascular risk. Methods and Results — We examined the relationship between diet and leptin in 2 related homogeneous African tribal populations of Tanzania. One tribe consumes freshwater fish as their main diet component (n=279), and the other tribe consumes a primarily vegetarian diet (n=329). In multivariate analysis, plasma leptin levels were associated with type of diet (F=14.3, P <0.001), independent of age, body mass index, body fat, alcohol consumption, or insulin. Both male (2.5±2 [fish diet] versus 11.2±2.4 [vegetarian diet] ng/mL, P =0.017) and female (5.0±1.9 [fish diet] versus 11.8±1.4 [vegetarian diet] ng/mL, P =0.007) fish eaters had lower plasma leptin levels than did their vegetable diet counterparts, even though body mass index values were virtually identical. Conclusions — A diet rich in fish is associated with lower plasma leptin, independent of body fat. These findings may have implications for understanding the reduced cardiovascular risk in subjects on a high-fish diet.
And the Answer Is, It Doesn’t Much Matter
Holmes, David R. , Gersh, Bernard J.

Circulation | July 28, 2002 | Volume: 106 | Issue: 1 | Pages: 11-13

10.1161/01.cir.0000024293.71103.3a | PMID 12093761 Get It

Establishment of standardised SLA/LP immunoassays: specificity for autoimmune hepatitis, worldwide occurrence, and clinical characteristics
Baeres, M, Herkel, Johannes , Czaja, Albert J. , Wies, Ingrid, Kanzler, Stephan, Cançado, Eduardo Luiz Rachid , Porta, Gilda , Nishioka, Mikio, Simon, Tracey G. , Daehnrich, Cornelia, Schlumberger, W, Galle, Peter R. , Lohse, Ansgar W. , Galle, Peter Robert

Gut | July 28, 2002 | Volume: 51 | Issue: 2 | Pages: 259-264

10.1136/gut.51.2.259 | PMID 12117891 Get It

Background: Antibodies to soluble liver antigen/liver pancreas (SLA/LP) are specific markers of autoimmune hepatitis. Their target antigen has recently been cloned. Aims: To establish standardised immunoassays using the recombinant antigen, and to assess the frequency and significance of seropositivity in patients from different countries. Methods: An enzyme linked immunoassay was developed using purified recombinant antigen and validated by testing sera from 200 healthy blood donors and 1026 patients with various liver and non-liver diseases. The assay was then applied to 454 sera from 419 patients with autoimmune hepatitis from different countries. All sera were also tested by inhibition immunoassay and western blot. Results: Antibodies were reliably detected by the recombinant immunoassay and occurred exclusively in patients with autoimmune liver disease. Twenty three of 149 patients from the USA (15%), 23/132 from Brazil (17%), 21/108 from Germany (19%), and 2/30 from Japan (7%) were seropositive. Clinical features at presentation were similar between seropositive and seronegative patients. However, relapse after corticosteroid withdrawal or during maintenance therapy occurred more commonly in seropositive patients. Conclusions: Antibodies to SLA/LP can be reliably detected by these standardised immunoassays based on recombinant antigen. Antibodies to SLA/LP occur with similar frequencies in different geographical regions, races, and age groups, and are of exquisite diagnostic specificity. Whether SLA/LP positive patients represent a clinically distinct subgroup remains to be determined; relapse during treatment reduction appeared to be more common in the SLA/LP group.
Randomized Controlled Trial of Yttrium-90–Labeled Ibritumomab Tiuxetan Radioimmunotherapy Versus Rituximab Immunotherapy for Patients With Relapsed or Refractory Low-Grade, Follicular, or Transformed B-Cell Non-Hodgkin’s Lymphoma
Gordon, Leo I. , Cabanillas, Fernando , Czuczman, Myron S., Emmanouilides, Christos, Pohlman, Brad , Bartlett, Nancy L. , Wiseman, Gregory A., Padre, Norman M., Grillo-López, Antonio J, Multani, Pratik S. , White, Christine A., Witzig, Thomas E. , Joyce, Robin , Gordon, Leo I , Bartlett, Nancy L

Journal of Clinical Oncology | July 27, 2002 | Volume: 20 | Issue: 10 | Pages: 2453-2463

10.1200/jco.2002.11.076 | PMID 12011122 Get It

PURPOSE: Radioimmunotherapy combines biologic and radiolytic mechanisms to target and destroy tumor cells, thus offering a needed therapeutic alternative for refractory non-Hodgkin’s lymphoma (NHL) patients. This phase III randomized study compares the novel radioimmunotherapy yttrium-90 (90Y) ibritumomab tiuxetan with a control immunotherapy, rituximab, in 143 patients with relapsed or refractory low-grade, follicular, or transformed CD20+transformed NHL.PATIENTS AND METHODS: Patients received either a single intravenous (IV) dose of90Y ibritumomab tiuxetan 0.4 mCi/kg (n = 73) or rituximab 375 mg/m2IV weekly for four doses (n = 70). The radioimmunotherapy group was pretreated with two rituximab doses (250 mg/m2) to improve biodistribution and one dose of indium-111 ibritumomab tiuxetan for imaging and dosimetry. The primary end point, overall response rate (ORR), was assessed by an independent, blinded, lymphoma expert panel.RESULTS: ORR was 80% for the90Y ibritumomab tiuxetan group versus 56% for the rituximab group (P = .002). Complete response (CR) rates were 30% and 16% in the90Y ibritumomab tiuxetan and rituximab groups, respectively (P = .04). An additional 4% achieved an unconfirmed CR in each group. Kaplan-Meier estimated median duration of response was 14.2 months in the90Y ibritumomab tiuxetan group versus 12.1 months in the control group (P = .6), and time to progression was 11.2 versus 10.1 months (P = .173) in all patients. Durable responses of ≥ 6 months were 64% versus 47% (P = .030). Reversible myelosuppression was the primary toxicity noted with90Y ibritumomab tiuxetan.CONCLUSION: Radioimmunotherapy with90Y ibritumomab tiuxetan is well tolerated and produces statistically and clinically significant higher ORR and CR compared with rituximab alone.