Zobrazeno 1 - 10
of 164
pro vyhledávání: '"David R. Lucas"'
Autor:
Eman Abdulfatah, Douglas Rottmann, Yoav Morag, Liron Pantanowitz, Aaron M. Udager, Wei Hao, David R. Lucas
Publikováno v:
Human Pathology. 136:63-74
Autor:
Steven M Hrycaj, Julianne M Szczepanski, Lili Zhao, Javed Siddiqui, Dafydd G Thomas, David R Lucas, Rajiv M Patel, Paul W Harms, Scott C Bresler, May P Chan
Publikováno v:
Histopathology. 81:818-825
Diagnosis of spindle cell/sarcomatoid melanoma may be challenging due to frequent loss of expression of melanocytic marker(s) and histomorphologic resemblance to various mesenchymal tumours, particularly malignant peripheral nerve sheath tumour (MPNS
Autor:
Laurence M Briski, Dafydd G Thomas, Rajiv M Patel, Elizabeth R Lawlor, Rashmi Chugh, Jonathan B McHugh, David R Lucas
Publikováno v:
Rare Tumors, Vol 10 (2018)
Background: Previous studies have shown that aberrant activation of the Wnt/β-catenin pathway is associated with many malignant neoplasms. This includes some soft-tissue sarcoma phenotypes, most notably synovial sarcoma, implicating potential target
Externí odkaz:
https://doaj.org/article/b9f6484c128047a0894f7eed3f89e25b
Autor:
Yoav Morag, David R. Lucas
Publikováno v:
Skeletal Radiology. 51:691-700
The ultrasound appearance of myxofibrosarcoma is highly variable corresponding to its variable and at times heterogeneous histopathologic appearance. Myxofibrosarcomas may mimic a benign process and the infiltrative tumor margins may be difficult to
Autor:
Dian Wang, Jonathan Harris, William G. Kraybill, Burt Eisenberg, David G. Kirsch, David S. Ettinger, John M. Kane, Parul N. Barry, Arash Naghavi, Carolyn R. Freeman, Yen-Lin Chen, Ying J. Hitchcock, Manpreet Bedi, Kilian E. Salerno, Diane Severin, Karen D. Godette, Nicole A. Larrier, Walter J. Curran, Pedro A. Torres-Saavedra, David R. Lucas
Publikováno v:
JAMA Oncology. 9:646
ImportancePathologic complete response (pCR) may be associated with prognosis in patients with soft tissue sarcoma (STS).ObjectiveWe sought to determine the prognostic significance of pCR on survival outcomes in STS for patients receiving neoadjuvant
Autor:
Jon A. Jacobson, William D. Middleton, Sandra J. Allison, Nirvikar Dahiya, Kenneth S. Lee, Benjamin D. Levine, David R. Lucas, Mark D. Murphey, Levon N. Nazarian, Geoffrey W. Siegel, Jason M. Wagner
Publikováno v:
Radiology. 304(1)
The Society of Radiologists in Ultrasound convened a panel of specialists from radiology, orthopedic surgery, and pathology to arrive at a consensus regarding the management of superficial soft-tissue masses imaged with US. The recommendations in thi
Publikováno v:
Sarcoma, Vol 9, Iss 3-4, Pp 141-145 (2005)
Purpose:This is the initial report on the utilization of combined photon irradiation followed by a neutron boost irradiation for the initial management of patients with high-grade non-metastatic soft tissue sarcoma (STS). We present data on local con
Externí odkaz:
https://doaj.org/article/7e9d692a1334490ba8c37882fb4b2000
Publikováno v:
Sarcoma, Vol 8, Iss 2-3, Pp 57-61 (2004)
Background: Patients who have had initial curative intent therapy for non-metastatic soft tissue sarcoma, and who subsequently relapse at the initial site without evidence of metastatic disease, have various options regarding local treatment. The tre
Externí odkaz:
https://doaj.org/article/5ea2960abe1e43f5a6af6920fc1b2c51
Autor:
Grace Y. Wang, David R. Lucas
Publikováno v:
Archives of Pathology & Laboratory Medicine. 143:1332-1337
Context.—Leiomyosarcoma of bone is a rare primary osseous sarcoma characterized by smooth muscle differentiation and absence of malignant osteoid formation. Leiomyosarcoma of bone is diagnostically challenging; this can be improved with greater awa
Autor:
Soo-Jin Cho, David R. Lucas, Jessica L. Davis, Scott M. Schuetze, Grace Y. Wang, Bryan L. Betz, Jonathan B. McHugh, Paul W. Harms, Tony Ng, Andrew E. Horvai, Rajiv M. Patel, Dafydd G. Thomas
Publikováno v:
American Journal of Surgical Pathology. 43:1112-1122
In recent years, a novel small round cell sarcoma harboring EWSR1-NFATC2 translocation with immunomorphologic overlap with Ewing sarcoma (ES), myoepithelial tumors, and extraskeletal myxoid chondrosarcoma has emerged. There has not been a case series