NTRK‐rearranged mesenchymal tumour with epithelioid features: expanding the morphological spectrum of NTRK‐fused neoplasms

2021 ◽  
Author(s):  
João Victor Alves de Castro ◽  
Felipe D’Almeida Costa ◽  
Giovana Tardin Torrezan ◽  
Dirce Maria Carraro ◽  
Ulisses Ribaldo Nicolau ◽  
...  
Keyword(s):  
Mesenchymal Tumour

scholarly journals Primary myxoid mesenchymal tumour with intracranial location: report of a case with a EWSR1 -ATF1 fusion

2018 ◽  
Vol 72 (5) ◽  
pp. 880-883 ◽  
Author(s):  
Raf Sciot ◽  
Sandra Jacobs ◽  
Frank Van Calenbergh ◽  
Philippe Demaerel ◽  
Agnieszka Wozniak ◽  
...  
Keyword(s):  
Mesenchymal Tumour

Benign mixed mesenchymal tumour of the ovary (or chondrolipoleiomyoma)

2003 ◽  
Vol 42 (2) ◽  
pp. 200-202
Author(s):  
C Womack ◽  
J M Randall
Keyword(s):  
Mesenchymal Tumour

scholarly journals Masa a nivel de íleon distal

2020 ◽  
Vol 50 (2) ◽  
Author(s):  
Nicolás Roccatagliata ◽  
Nebil Larrañaga ◽  
Germán Espil ◽  
Roberto Salgado (H) ◽  
Jairo Hernández Pinzón ◽  
...  
Keyword(s):  
Small Bowel ◽  
Digestive Tract ◽  
Bowel Obstruction ◽  
Mesenchymal Tumour ◽  
Frequent Localization

GIST is the most common mesenchymal tumour in the digestive tract. One of the most frequent localization is at the small bowel (30%), and one of its unusual forms of presentation is as a bowel obstruction. The purpose of this article is to report a case of bowel obstruction secondary to a GIST and the adopted conduct.

Identification of a novelFN1-FGFR1genetic fusion as a frequent event in phosphaturic mesenchymal tumour

2015 ◽  
Vol 235 (4) ◽  
pp. 539-545 ◽  
Author(s):  
Jen-Chieh Lee ◽  
Yung-Ming Jeng ◽  
Sheng-Yao Su ◽  
Chen-Tu Wu ◽  
Keh-Sung Tsai ◽  
...  
Keyword(s):  
Mesenchymal Tumour ◽  
Frequent Event ◽  
Phosphaturic Mesenchymal Tumour

Unique case of metachronous adrenal and hepatic myelolipomas

2021 ◽  
Vol 14 (3) ◽  
pp. e240894
Author(s):  
Paul David Morris ◽  
Chow P'Ng ◽  
Henry Pleass
Keyword(s):  
Adrenal Gland ◽  
Postoperative Period ◽  
Case Reports ◽  
Unique Case ◽  
Mesenchymal Tumour

We present a unique case of metachronous adrenal and hepatic myelolipomas in a 62-year-old man. Myelolipomas are most commonly found in the adrenal gland, with extra-adrenal sites such as the lung, retroperitoneum and liver reported. They are a form of benign mesenchymal tumour, with only 25 case reports of a hepatic location published to date. The are no guidelines to its management. Our patient underwent resection due to pain, and after a complicated postoperative period is pain free.

Phosphaturic mesenchymal tumour: an interesting diagnostic and surgical case of tumour‐induced osteomalacia

2020 ◽  
Vol 90 (9) ◽  
pp. 1812-1814
Author(s):  
Jock Clarnette ◽  
Jakub Jagiello ◽  
Gelareh Farshid ◽  
Richard Smith
Keyword(s):  
Mesenchymal Tumour ◽  
Surgical Case ◽  
Phosphaturic Mesenchymal Tumour

scholarly journals Partial cystectomy: Is it a reliable option for the treatment of bladder

2013 ◽  
Vol 5 (1) ◽  
pp. 11 ◽  
Author(s):  
Yun-fei Xu ◽  
Guang-chun Wang ◽  
Jun-hua Zheng ◽  
Bo Peng
Keyword(s):  
Quality Of Life ◽  
Young Patients ◽  
Partial Cystectomy ◽  
Mesenchymal Tumour ◽  
Center Stage ◽  
Primary Bladder

Bladder leiomyosarcoma is a unique mesenchymal tumour,accounting for less than 0.5% of all primary bladder malignancies.Bladder leiomyosarcoma used to be treated with radical surgeryin either old or young patients, often resulting in significantimpact on the patients’s quality of life after surgery. We reporton a case of bladder leiomyosarcoma in a 31-year-old femalewho was treated with partial cystectomy. Fortunately, no tumourmetastasis or relapse was observed during the 7-year follow-upperiod and the patient now has a good quality of life. We foundthat partial cystectomy may be an acceptable option to treat bladderleiomyosarcoma in the low MSKCC (Memorial Sloan-KetteringCancer Center) stage.

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