Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Leiomyoblastomas"'
Autor:
Ghaith Barefah, Arwa Ahmed Ashoor
Publikováno v:
BMJ Case Reports
Gastrointestinal stromal tumour (GIST) is a recent recognised tumour entity. In the past, those tumours were classified as leiomyomas, leiomyosarcomas and leiomyoblastomas, but it is now evident that GIST is a separate tumour entity and is the most c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2535e495cda8197877646be7bcb8a3d0
https://doi.org/10.1136/bcr-2019-229839
https://doi.org/10.1136/bcr-2019-229839
Autor:
Mary E. Falcone
Publikováno v:
Journal of Diagnostic Medical Sonography. 28:131-134
Gastrointestinal stromal tumors or GISTs belong to a category of gastrointestinal mesenchymal tumors that can have benign or malignant potential. These tumors were formerly identified as gastrointestinal (GI) leiomyomas, leiomyoblastomas, or leiomyos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b584e3afe0bddca4841395ea2d8d5014
https://doi.org/10.1177/8756479312440621
https://doi.org/10.1177/8756479312440621
Publikováno v:
European Journal of Radiology. 60:431-438
Gastrointestinal stromal tumours (GISTs) are a rare group of mesenchymal neoplasms that occur predominantly in the gastrointestinal tract. Previously GISTs were classified as smooth muscle tumours referred to as leiomyomas, leiomyosacromas or leiomyo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c9827d8417fc7b3bec16936b4511f89
https://doi.org/10.1016/j.ejrad.2006.06.017
https://doi.org/10.1016/j.ejrad.2006.06.017
Publikováno v:
Sarcoma
Sarcoma, Vol 3, Iss 1, Pp 5-9 (1999)
Sarcoma, Vol 3, Iss 1, Pp 5-9 (1999)
Purpose. Epithelioid leiomyoblastomas comprise the majority of gastric sarcomas and are uncommon in other parts of the gastrointestinal tract. Diagnosis of this lesion by fine-needle aspiration cytology has been occasionally described in the literatu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89e673659e8d6492d1af12df0238df2b
https://doi.org/10.1080/13577149977802
https://doi.org/10.1080/13577149977802
Publikováno v:
BMJ case reports. 2011
Gastrointestinal stromal tumours (GISTs) are a subset of gastrointestinal (GI) mesenchymal tumours of varying differentiation and represent 1-3% of all gastrointestinal malignancies--70% occur in the stomach. Previously, these tumours were classified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7f665c5795bad26ae0fc09b48c31f80
https://pubmed.ncbi.nlm.nih.gov/22707491
https://pubmed.ncbi.nlm.nih.gov/22707491
Autor:
Toshihiko Ooguri, Mitsuhiro Kida, Tomoya Kan, Katsunori Saigenji, Yukihito Yamada, Makoto Noto, Tetsuaki Sakaguchi, Hidenaga Uesugi
Publikováno v:
Digestive Endoscopy. 4:396-408
Seventy-six myogenic tumors (60 leimyomas, 3 leiomyoblastomas, 13 leiomyosarcomas) surgically resected from the upper gastrointestinal tract were studied histopathologically to define the characteristics of benign and malignant tumors. Twenty-nine of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e60606c6f6540ac3b88a3bea05b9e0b8
https://doi.org/10.1111/j.1443-1661.1992.tb00105.x
https://doi.org/10.1111/j.1443-1661.1992.tb00105.x
Publikováno v:
Onkologie. 30(12)
Gastrointestinal stromal tumors (GIST) comprise a majority of tumors previously diagnosed as gastrointestinal leiomyomas, leiomyoblastomas, and leiomyosarcomas. Although GIST may be identified by light microscopy, pathologists commonly employ a panel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e44f097de7a840b5911a2349200e2d21
https://pubmed.ncbi.nlm.nih.gov/18063877
https://pubmed.ncbi.nlm.nih.gov/18063877
Publikováno v:
Journal of Pediatric Surgery. 26:225-227
A case of gastric leiomyoblastoma in a 7-year-old girl, who underwent partial gastrectomy combined with complete removal of perigastric lymph nodes, is reported. Characteristics of the behavior and prognosis of gastric leiomyoblastomas in childhood a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f0c2a51bbce23dc9970a83f9b473970
https://doi.org/10.1016/0022-3468(91)90919-k
https://doi.org/10.1016/0022-3468(91)90919-k
Publikováno v:
Respiratory medicine. 90(2)
Multiple pulmonary chondromatous hamartomas (MPCH) are rare, and MPCH with tracheal involvement have not been, to the best of our knowledge, reported before. Furthermore, there is no agreement in the literature about the origin of these tumours. We r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29b0b3e337f44c7e657ae10e7ce04502
https://pubmed.ncbi.nlm.nih.gov/8730331
https://pubmed.ncbi.nlm.nih.gov/8730331
Autor:
Vlasta Rychterova, Inga Hägerstrand
Publikováno v:
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica. 99(11)
Two cases of parietal cell carcinoma are reported and compared with seven cases previously described. Eight of nine patients have been male. The tumours grow mainly outside the mucosa and can macro- and microscopically be misinterpreted as leiomyobla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5646af033c4438c8043a78750a414a0a
https://pubmed.ncbi.nlm.nih.gov/1958345
https://pubmed.ncbi.nlm.nih.gov/1958345