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  • Book
    Ritu Nayar, Xiaoqi Lin, Ajit S. Paintal, Ramona Gupta, Albert A. Nemcek Jr., editors.
    Summary: The diagnostic services, pathology and radiology, are the cornerstone for supporting the delivery of high-quality healthcare by providing timely and accurate diagnosis. In this era of precision medicine, it has become increasingly important for these two services to work collaboratively in supporting patients and clinical colleagues by informing and communicating the selection and interpretation of appropriate diagnostic tests, as well as obtaining adequate tissue for diagnosis, prognostication, and therapy at initial presentation and, if required, during disease progression/relapse. This book is aimed at practicing cytopathologists and interventional radiologists as well as trainees in these areas. An essential requirement in the accurate diagnosis of these mass lesion biopsies is the correlation of cytomorphology with the radiological findings and adequate triage of acquired material during the biopsy procedure. The cytologic findings, gross surgically resected specimens, and imaging findings are illustrated to provide a complete pathologic-radiologic correlation of the entities discussed. This Atlas of Cytopathology and Radiology serves as a useful guide for pathologists and radiologists in the appropriate triage and diagnosis of deep seated mass lesions biopsied under ultrasound, CT Scan or fluoroscopic guidance.

    Contents:
    An Introduction to Radiology and Cytopathology Considerations in a Collaborative Biopsy Service
    Liver
    Lungs, Mediastinum, and Pleura
    Lymph Nodes and Spleen
    Kidney, Adrenal Gland, and Paraganglia
    Pelvis, Peritoneum, and Omentum
    Esophagus, Gastrointestinal Tract, and Pancreas
    Thyroid, Parathyroid, Head, and Neck
    Salivary Glands
    Bone and Soft Tissue Tumors
    The Breast.
    Digital Access Springer 2020
  • Article
    Nakamoto Y, Dohi K, Fujike H, Yuri T, Shinoda A, Takeuchi J.
    Kidney Int. 1978 Apr;13(4):297-305.
    Unilateral progressive Masugi nephritis was produced in rabbits and studied by microangiography as well as light and immunofluorescence microscopy. The following five groups were studied: Group 1. Heparin was started simultaneously with nephrotoxic serum (NTS) and was given for one week. The animals were then sacrificed along with the untreated controls. Group 2. This was the same protocol as in group 1 but with three weeks' heparin. Group 3. Heparin was started one day after NTS was given for three weeks. Group 4. Heparin was started one to two weeks after NTS and was given for three weeks. Group 5: late effect group. Heparin was started simultaneously with NTS, was given for four weeks, and the animals were then sacrificed 10 to 13 weeks later. Heparin dose was 5,000 U, s.c., per day in all treated groups. The number of glomeruli seen per unit of cortex by microangiography was significantly increased in the first through the third groups, as compared to the controls. Group 1 did not show this increase but there was some decrease of immunofluorescent fibrinogen. The late effect group (group 5) showed no modification by the treatment, suggesting that an initial improvement may have been negated by persistent immunologic insults after heparin withdrawal.
    Digital Access Access Options