Zobrazeno 1 - 10
of 508
pro vyhledávání: '"Mesenchymal neoplasm"'
Autor:
Sudeep KC, MD, Himani Poudyal, MBBS
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4363-4368 (2024)
Solitary fibrous tumor (SFT) arising from adult mesenchymal stem cells is an uncommon vascular tumor of pelvic cavity. While initially thought to be confined to the pleura, pericardium, or peritoneum, recent studies have revealed that SFTs can develo
Externí odkaz:
https://doaj.org/article/73e9a4b321824fb08fb4199068cfc8d1
Publikováno v:
National Journal of Laboratory Medicine, Vol 13, Iss 03, Pp 08-12 (2024)
Undifferentiated Embryonal Sarcoma of the Liver (UESL) is a rare hepatic malignant mesenchymal neoplasm in the paediatric population, typically affecting children between 6-10 years of age without sex predilection. It accounts for 9-15% of paediatric
Externí odkaz:
https://doaj.org/article/bc02b2d3b3dc4e03ac3efe0a9c6e9f41
Autor:
Narayanamoorthy Keerthyraj, Vigneswaramoorthi Vinayagamoorthi, Erli Amel Ivan, V Sriram, Govindasamy Revathi, Ramya Gandhi
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 17, Iss Suppl 1, Pp S219-S223 (2024)
Endometrial stromal tumors are rare uterine mesenchymal neoplasms. Endometrial stromal sarcomas (ESSs) are of endometrial stromal origin that accounts for approximately 1% of all uterine malignant neoplasms. ESS is classified into endometrial stromal
Externí odkaz:
https://doaj.org/article/0857e4befebf49e69bcc29e47e346a0a
Publikováno v:
Diagnostics, Vol 14, Iss 12, p 1271 (2024)
Uterine tumor resembling ovarian sex-cord tumor (UTROSCT) is a rare form of uterine mesenchymal neoplasm. Although UTROSCT generally exhibits benign behavior with a favorable prognosis, this neoplasm is nevertheless classified as being of uncertain m
Externí odkaz:
https://doaj.org/article/5df261eda89e4d80b8c6aa6dcd81f8c3
Autor:
Prachi, Hema Malini Aiyer
Publikováno v:
Surgical and Experimental Pathology, Vol 6, Iss 1, Pp 1-3 (2023)
Abstract Sclerosing Epithelioid Fibrosarcoma is a rare form of soft tissue sarcoma, with increased propensity for local recurrence and metastases mainly pulmonary and pleural in about 50% of cases. It carries morphological resemblance with many sarco
Externí odkaz:
https://doaj.org/article/e6ae06db886b4261ab7c6dd8dee37f64
Publikováno v:
Clinical Case Reports, Vol 11, Iss 6, Pp n/a-n/a (2023)
Key Clinical Message Intramuscular myxoma (IMM) is a benign soft tissue tumor of mesenchymal origin that occurs mainly in skeletal muscles which can be removed through surgery after diagnosis. Abstract Intramuscular myxoma (IMM) is a benign soft tiss
Externí odkaz:
https://doaj.org/article/bf8a750ddc8f42889456f90615fa8978
Publikováno v:
Bone Reports, Vol 18, Iss , Pp 101685- (2023)
Mazabraud's syndrome represents rare benign disorder characterized by simultaneous occurrence of fibrous dysplasia of bone and intramuscular myxomas within surrounding soft tissue. Mutations of GNAS1 gene were proven to be causative for this conditio
Externí odkaz:
https://doaj.org/article/b2358477b7fd456a8162e08c6042a364
Akademický článek
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Akademický článek
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Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 4, Pp PD01-PD05 (2023)
Aggressive Angiomyxoma is most commonly identified as a slow growing mesenchymal neoplasm most commonly seen in women than in men. It has a marked tendency for local recurrence but with low instances of metastasis. Radiological investigations may ass
Externí odkaz:
https://doaj.org/article/6f0b3de844d84379bd7a5314390c1b71