Zobrazeno 1 - 10
of 341
pro vyhledávání: '"A. L., Folpe"'
Autor:
Tomas V. Gonzalez, MD, Tiffany M. Sae-Kho, MD, Steven I. Robinson, MBBS, Tina J. Hieken, MD, Andrew L. Folpe, MD, Stephen M. Broski, MD, Amy C. Degnim, MD, Katrina N. Glazebrook, MB, ChB
Publikováno v:
Radiology Case Reports, Vol 17, Iss 10, Pp 3624-3629 (2022)
Radiation-associated angiosarcoma of the breast (RAASB) is a rare and aggressive malignancy occurring after radiation therapy as part of breast cancer treatment. RAASB usually presents several years after prior radiation and typically involves the sk
Externí odkaz:
https://doaj.org/article/a4bab0badc884c98a411529aa51dd84e
Autor:
Megan M. Jack, Brandon W. Smith, Christopher J. Klein, Taxiarchis Kourelis, Andrew L. Folpe, Robert J. Spinner, Ellen D. McPhail
Publikováno v:
Interdisciplinary Neurosurgery, Vol 26, Iss , Pp 101301- (2021)
Systemic amyloid light-chain amyloidosis is a protein misfolding disorder characterized by extracellular deposition of amyloid fibrils derived from abnormal clonal immunoglobulin light chains in various organ systems. While amyloid light-chain amyloi
Externí odkaz:
https://doaj.org/article/3508b43cde6f493090ec50492930751e
Autor:
Juan M. Colazo, BSc, Joseph A. DeCorte, BS, Erin A. Gillaspie, MD, MPH, Andrew L. Folpe, MD, Kathryn M. Dahir, MD
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 100744- (2021)
Tumor-induced osteomalacia (TIO), caused by phosphaturic mesenchymal tumors (PMTs), is a rare paraneoplastic syndrome characterized by frequent bone fractures, bone pain, muscle weakness, and affected gait. These tumors typically secrete high levels
Externí odkaz:
https://doaj.org/article/ce3ae98c10d64f2395f285204805e65c
Publikováno v:
Journal of Surgical Research. 283:982-991
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2020 (2020)
Angiosarcoma of the colon is rare, as is colonic amyloidosis. To our knowledge, there have been no reported cases of angiosarcoma arising in association with amyloid deposition. Herein, we described a case of 77-year-old man who presented with hemato
Externí odkaz:
https://doaj.org/article/1b7acfb323354031bfbf1bf4ef024332
Autor:
Matthew T. Houdek, Katherine E. Mallett, Mark J. Heidenreich, Safia K. Ahmed, Doris E. Wenger, John‐Rudolph H. Smith, Brittany L. Siontis, Steven I. Robinson, Andrew L. Folpe, Ivy A. Petersen, Peter S. Rose
Publikováno v:
Journal of Surgical Oncology. 127:848-854
Compared to other sarcomas, myxoid liposarcoma (ML) is known to be radiosensitive, with improved oncologic outcomes. Although these tumors "shrink" following radiotherapy, there is a paucity of data examining the degree of radiosensitivity and oncolo
Autor:
Sounak Gupta, Andrew L. Folpe, Jorge Torres-Mora, Victor E. Reuter, Jonathan E. Zuckerman, Nadja Falk, Melissa L. Stanton, Selvaraj Muthusamy, Steven C. Smith, Vidit Sharma, Sanjeev Sethi, Loren Herrera-Hernandez, Rafael E. Jimenez, John C. Cheville
Publikováno v:
Human Pathology. 128:110-123
Juxtaglomerular cell tumors and glomus tumors both arise from perivascular mesenchymal cells. Juxtaglomerular cells are specialized renin-secreting myoendocrine cells in the afferent arterioles adjacent to glomeruli, and juxtaglomerular tumors derive
Autor:
Mira M. Lotfalla, Andrew L. Folpe, Karen J. Fritchie, Patricia T. Greipp, Gretchen G. Galliano, Kevin C. Halling, Taofic Mounajjed, Jorge Torres-Mora, Rondell P. Graham
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2019 (2019)
Epithelioid hemangioendothelioma (EHE) is an uncommon low-grade malignant vascular tumor that may arise in soft tissue/bone or visceral sites such as the liver and lung. As this tumor exhibits epithelioid morphology, it frequently causes diagnostic c
Externí odkaz:
https://doaj.org/article/0bdc92130ba446cabf28ea26b877971b
Publikováno v:
Sarcoma, Vol 2019 (2019)
Purpose. Previous studies have grouped the treatment of axial and appendicular synovial sarcomas. The purpose of this study was to assess the prognostic variables of upper extremity synovial sarcomas (UESS) and compare the outcomes of those who under
Externí odkaz:
https://doaj.org/article/24202aa6a5b74c39a480f6ee25347bb4
Publikováno v:
Journal of Cutaneous Pathology. 50:220-222