Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Jeanne M. Meis"'
Autor:
Laura M. Warmke, Jeanne M. Meis
Publikováno v:
Human Pathology Reports, Vol 26, Iss , Pp 300552- (2021)
Round cell sarcomas with EWSR1-non-ETS fusions are a rare group of sarcomas, entirely distinct from Ewing sarcoma with canonical fusion, of which EWSR1-PATZ1-rearranged sarcomas are emerging as a distinct entity. Only a few cases of this sarcoma have
Externí odkaz:
https://doaj.org/article/12fd5cb52e914db3858e0976a537f0af
Publikováno v:
Rare Tumors, Vol 6, Iss 4 (2014)
Extraskeletal myxoid chondrosarcoma is a rare soft tissue neoplasm that occurs predominantly in the soft tissues of the lower extremities. Herein we present a case of a 29 year old male who presented with bilateral femoral numbness believed to be the
Externí odkaz:
https://doaj.org/article/b8e41a76ddf547eeb8ad92bf78007fa4
Autor:
Veronica Ulici, Jason L. Hornick, Jessica L. Davis, Swati Mehrotra, Jeanne M. Meis, Kevin C. Halling, Christopher D.M. Fletcher, Erica Kao, Andrew L. Folpe
Publikováno v:
Modern Pathology. 36:100160
Autor:
Carina A. Dehner, Katherine Geiersbach, Ross Rowsey, Paari Murugan, Stephen Broski, Jeanne M. Meis, Andrew E. Rosenberg, Andrew L. Folpe
Publikováno v:
Modern Pathology. 36:100131
Autor:
Harry S. Cooper, Xuefeng Zhang, John Hart, John R. Goldblum, Reet Pai, Elizabeth Yiru Wu, Teri A. Longacre, Wendy L. Frankel, Marie E. Robert, Sang Mee Lee, Michael Feely, Rhonda K. Yantiss, Gregory Y. Lauwers, Catherine Hagen, Hanlin L. Wang, Nicole C. Panarelli, Sherry Tang, Rish K. Pai, Mary P. Bronner, Rajeswari Nagarathinam, Mohammed Alsomali, Shaomin Hu, Courtney Thomas, Laura W. Lamps, Joseph Misdraji, Raul S. Gonzalez, Shefali Chopra, Zu-Hua Gao, Lei Zhao, Theresa Smith, Jeanne M. Meis, Vanessa L. Smith, Ahmed Bakhshwin, David S. Klimstra, Diana Agostini-Vulaj, Shyam S. Raghavan, Jing Bo Wu, Mohamed E. Mostafa, Jinru Shia, Erika Hissong, Ram Al-Sabti, Sanjay Kakar, Murray B. Resnick, Lindsay Alpert, Naziheh Assarzadegan, Joel K. Greenson, Rondell P. Graham, Lindsey M Westbrook, Andrew M. Bellizzi, Leona A. Doyle, Gokce Askan, Masoumeh Ghayouri, Deyali Chatterjee, Angela R. Shih, Zachary Dong, Liang I. Kang, Mojgan Hosseini, Juan Rong, Sindhu Shetty
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, vol 33, iss 7
Mod Pathol
Mod Pathol
Smooth muscle tumors represent the second most common mural mesenchymal neoplasm in the gastrointestinal tract, but established criteria for prognostic assessment of these tumors are lacking. A large cohort of surgically resected intramural gastroint
Autor:
Leomar Y. Ballester, Jeanne M. Meis, Kimberly B Hoang, Gregory N. Fuller, Alexander J. Lazar, Norman E. Leeds, Sujit S. Prabhu
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 79:347-351
Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor that arises primarily in the extremities of young adults. Recurrent gene fusions involving EWSR1 with members of the cAMP response element binding protein (CREB) family have been repo
Autor:
Jing Wang, Wei-Lien Wang, Hongxia Sun, Lei Huo, Yun Wu, Hui Chen, Qiong Gan, Jeanne M. Meis, Nolan Maloney, Alexander J. Lazar, Esther C. Yoon, Constance T. Albarracin, Savitri Krishnamurthy, Lavinia P. Middleton, Erika Resetkova, Wendong Yu, Dongfeng Tan, Wei Lu, Luisa Maren Solis Soto, Shufang Wang, Ignacio I. Wistuba, Anil V. Parwani, Victor G. Prieto, Aysegul A. Sahin, Zaibo Li, Qingqing Ding
Publikováno v:
Human pathology. 121
When a sarcomatous neoplasm is identified in the breast, distinguishing metaplastic carcinoma, malignant phyllodes tumor (MPT), and primary sarcoma is a diagnostic challenge, especially on small biopsies, as all these tumors may have overlapping morp
Autor:
Jae Y. Ro, Arthur W. Zieske, Alberto G. Ayala, Jeanne M. Meis, Jessica Tomsula, Jacqueline Monheit, Robert D. Koy
Publikováno v:
Annals of Diagnostic Pathology. 40:13-17
Autor:
Jeanne M. Meis, Laura Warmke
Publikováno v:
The American journal of surgical pathology. 45(3)
Since its original description in 1995, the concept of sclerosing epithelioid fibrosarcoma (SEF) as a distinctive tumor has evolved in the literature. Subsequent studies suggested that the presence of low grade fibromyxoid sarcoma (LGFMS)-like zones,
Autor:
Angshumoy Roy, Anthony P. Conley, Jacquelyn Reuther, Behrang Amini, J. Andrew Livingston, Wei-Lien Wang, Jeanne M. Meis, Yulei Shen, Christian Curcio, Laurence D. Rhines, Megan Dupuis, Kevin E. Fisher
Publikováno v:
Clinical Sarcoma Research, Vol 10, Iss 1, Pp 1-7 (2020)
Clinical Sarcoma Research
Clinical Sarcoma Research
Background Lipofibromatosis-like neural tumors (LPF-NT) are a newly identified class of rare mesenchymal neoplasms. Current standard of care therapy is surgical resection alone; there are no chemotherapies or molecular targeted therapies that have be