Results 41 to 50 of about 456,696 (362)
Computer-Aided Diagnosis of Low Grade Endometrial Stromal Sarcoma (LGESS) [PDF]
arXiv, 2021 Low grade endometrial stromal sarcoma (LGESS) is rare form of cancer, accounting for about 0.2% of all uterine cancer cases. Approximately 75% of LGESS patients are initially misdiagnosed with leiomyoma, which is a type of benign tumor, also known as fibroids.
arxiv
Intraduodenal sarcoma recurrence of retroperitoneal origin: an unusual cause for a duodenal obstruction. [PDF]
, 2012 Soft tissue sarcomas are uncommon tumors, and intraduodenal soft tissue sarcoma manifestation is even more rare. Only three cases of intraduodenal sarcomas have been reported in the literature thus far.
Bao, Jean J +5 more
core +1 more source
Case Reports in Oncological Medicine, 2015 We describe two cases of florid, foreign body granulomatous reaction occurring in the upper arms of males in their eighth decade, who were undergoing treatment with depot injection of leuprorelin acetate for prostatic carcinoma.
Khin Thway +3 more
doaj +1 more source
Dermatofibrosarcoma protuberans: from translocation to targeted therapy
Cancer Biology & Medicine, 2015 Dermatofibrosarcoma protuberans (DFSP), the most common dermal sarcoma, is a low-grade, slow growing fibroblastic malignant neoplasm that most frequently affects middle aged adults and is characterized by a high local recurrence rate and a low propensity
Jonathan Noujaim +3 more
doaj +1 more source
Local Hydration Control and Functional Implications Through S-Nitrosylation of Proteins: Kirsten rat sarcoma virus (KRAS) and Hemoglobin (Hb) [PDF]
arXiv, 2022 S-nitrosylation, the covalent addition of NO to the thiol side chain of cysteine, is an important post-transitional modification (PTM) that can affect the function of proteins. As such, PTMs extend and diversify protein functions and thus characterizing consequences of PTM at a molecular level is of great interest. Although PTMs can be detected through
arxiv
Synovial sarcoma: the misdiagnosed sarcoma
EFORT Open ReviewsSynovial sarcoma is a rare and highly malignant soft tissue sarcoma. The inconspicuous and diversity of its early symptoms make it a highly misdiagnosed disease. The management of synovial sarcomas is challenging as they are rare and have a poor prognosis. Early and correct diagnosis and treatment are critical for clinical outcomes.
Chengxiang Li +4 more
openaire +2 more sources
European Journal of Medical Research, 2022 Background Desmoids are rare fibroblastic tumours whose treatment in any individual case presents a persistent challenge. We endeavoured to evaluate various clinicopathological factors contributing to tumour behaviour.
Misbah Khan +3 more
doaj +1 more source
Conformational Fluctuations and Phases in Fused in Sarcoma (FUS) Low-Complexity Domain [PDF]
arXiv, 2023 The well known phenomenon of phase separation in synthetic polymers and proteins has become a major topic in biophysics because it has been invoked as a mechanism of compartment formation in cells, without the need for membranes. Most of the coacervates (or condensates) are composed of Intrinsically Disordered Proteins (IDPs) or regions that are ...
arxiv
Rare Tumors, 2017 Myoepithelial tumors of the soft tissues represent a rare group of neoplasms that vary in their clinical behavior, pathologic features and genetics. They are histopathologically typified by a myoepithelial immunohistochemical phenotype, of expression of ...
Khin Thway +4 more
doaj +1 more source
Soft Tissue Sarcoma Co-Segmentation in Combined MRI and PET/CT Data [PDF]
arXiv, 2020 Tumor segmentation in multimodal medical images has seen a growing trend towards deep learning based methods. Typically, studies dealing with this topic fuse multimodal image data to improve the tumor segmentation contour for a single imaging modality. However, they do not take into account that tumor characteristics are emphasized differently by each ...
arxiv