Zobrazeno 1 - 10
of 54
pro vyhledávání: '"S W, WEISS"'
Autor:
Andrea T. Deyrup, S W Weiss
Publikováno v:
Histopathology. 48:42-50
By identifying patients at greatest risk for distant metastasis and, hence, most likely to benefit from adjuvant therapy, the grading of sarcomas has been one of the most important contributions pathologists have made to the treatment of sarcomas. Ov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7d00da57fb6259c970da905d955dc12
https://doi.org/10.1111/j.1365-2559.2005.02288.x
https://doi.org/10.1111/j.1365-2559.2005.02288.x
Publikováno v:
Histopathology. 45:245-253
Intra-abdominal synovial sarcoma: a clinicopathological study Aims: To evaluate a series of synovial sarcomas arising in the abdomen, pelvic cavity, or retroperitoneum. Synovial sarcoma is rare within the abdomen. In this location, it can be confused
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86c23e993228e7bd665fb9886e59f635
https://doi.org/10.1111/j.1365-2559.2004.01950.x
https://doi.org/10.1111/j.1365-2559.2004.01950.x
Publikováno v:
Histopathology. 45(5)
Aims: Alveolar soft part sarcoma (ASPS) is a rare sarcoma in the buttocks or thigh of young adults, often with metastases to lung, brain, or bone. This study examines the morphological and clinical features of lingual ASPS. Methods and results: Fourt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f48f8a0144a40b917d7c823417f8753
https://pubmed.ncbi.nlm.nih.gov/15500657
https://pubmed.ncbi.nlm.nih.gov/15500657
Autor:
J L, Arbiser, R, Yeung, S W, Weiss, Z K, Arbiser, M B, Amin, C, Cohen, D, Frank, S, Mahajan, G S, Herron, J, Yang, H, Onda, H B, Zhang, X, Bai, E, Uhlmann, A, Loehr, H, Northrup, P, Au, I, Davis, D E, Fisher, D H, Gutmann
Publikováno v:
The American journal of pathology. 159(2)
Angiomyolipomas are benign tumors of the kidney derived from putative perivascular epithelioid cells, that may undergo differentiation into cells with features of melanocytes, smooth muscle, and fat. To gain further insight into angiomyolipomas, we h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::305539bd5148dce4e344908ff60c21e2
https://pubmed.ncbi.nlm.nih.gov/11485907
https://pubmed.ncbi.nlm.nih.gov/11485907
Autor:
A L, Folpe, S W, Weiss
Publikováno v:
Seminars in diagnostic pathology. 17(4)
Paratesticular soft tissue tumors are uncommon neoplasms that may present significant challenges for the pathologist and clinician. This article reviews the incidence of these rare tumors, and on the common benign and malignant entities that occur in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9509314e25aeb05899d59429c14a5b63
https://pubmed.ncbi.nlm.nih.gov/11202547
https://pubmed.ncbi.nlm.nih.gov/11202547
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 12(9)
Although "giant cell tumor of soft parts" has traditionally been considered a single entity as reflected in the original term "malignant giant cell tumor of soft parts (MGCT)" and later by the term "malignant fibrous histiocytoma, giant cell type" th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81c8f4663c3564dd80a7738ddee9b438
https://pubmed.ncbi.nlm.nih.gov/10496598
https://pubmed.ncbi.nlm.nih.gov/10496598
Autor:
S W, Weiss
Publikováno v:
Verhandlungen der Deutschen Gesellschaft fur Pathologie. 82
Liposarcoma is one of the most common adult soft tissue sarcomas. It is best viewed as several related tumors rather than a common one, however. Support for this is derived from the fact that the various subtypes differ in their demographic, cytogene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5143b157d03c7ccc2c1b2ff358211c2
https://pubmed.ncbi.nlm.nih.gov/10095419
https://pubmed.ncbi.nlm.nih.gov/10095419
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 11(10)
Diffuse tenosynovial giant cell tumor (DGCT) could present as a large intra-articular mass (pigmented villonodular synovitis, or PVNS) or as an extraarticular mass, which might be confused with a sarcoma, particularly when growth is destructive and g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::33a1b8d0a4868808ee22131dbc22b451
https://pubmed.ncbi.nlm.nih.gov/9796719
https://pubmed.ncbi.nlm.nih.gov/9796719
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 11(4)
We report 51 cases of a previously undescribed tumor of the distal extremities that is often mistaken for an inflammatory or infectious process, Hodgkin's disease, or various sarcomas. These lesions developed in patients of all ages (range, 4-81 yr;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f248ba366e64b788a0e919df58fe6ead
https://pubmed.ncbi.nlm.nih.gov/9578090
https://pubmed.ncbi.nlm.nih.gov/9578090
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 11(4)
The inflammatory myofibroblastic tumor (IMT) is a distinctive but controversial lesion, usually occurring during childhood, composed of fascicles of bland myofibroblastic cells admixed with a prominent inflammatory infiltrate consisting of lymphocyte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::86a00e1c924c9e28d3dc414ebe1684d2
https://pubmed.ncbi.nlm.nih.gov/9578087
https://pubmed.ncbi.nlm.nih.gov/9578087