Results 11 to 20 of about 40,218 (214)

Stathmin expression alters the antiproliferative effect of eribulin in leiomyosarcoma cells

open access: yesJournal of Pharmacological Sciences, 2022
Uterine leiomyosarcoma is an aggressive soft tissue tumor. Stathmin, a phosphoprotein that modulates microtubule dynamics, is highly expressed in many malignancies including leiomyosarcoma.
Mana Azumi   +5 more
doaj   +1 more source

Primary vaginal leiomyosarcoma, a rare tumour: case report and review [PDF]

open access: yes, 2017
Primary vaginal leiomyosarcomas (pvLMS) are rare, recurrent tumours accounting for ca. 2% of all vaginal cancers. The etiology is still unknown, the prognosis is poor and there is no consensus guideline on its management.
Battaglione, Ezio   +3 more
core   +2 more sources

Choroidal metastasis from leiomyosarcoma in two cases

open access: yesOman Journal of Ophthalmology, 2014
Leiomyosarcoma is a malignant tumor of mesenchymal cells and is the most common soft-tissue sarcoma. Leiomyosarcoma is a notably rare tumor in the ophthalmic region and can be of primary, secondary or metastatic origin.
Eric Feinstein   +4 more
doaj   +1 more source

Surgical management for giant bladder leiomyosarcoma

open access: yesUrology Case Reports, 2022
While urothelial carcinoma is the most common histologic type of bladder cancer in the United States, leiomyosarcoma is a rare and aggressive variant. The rarity of bladder leiomyosarcoma results in uncertainty regarding the optimal treatment pathway. We
Alexander A. Hart   +4 more
doaj   +1 more source

Associations of clock genes polymorphisms with soft tissue sarcoma susceptibility and prognosis [PDF]

open access: yes, 2018
BACKGROUND: Dysfunction of the circadian clock and polymorphisms of some circadian genes have been linked to cancer development and progression. We investigated the relationship between circadian genes germline variation and susceptibility or prognosis ...
Benna, Clara   +6 more
core   +2 more sources

Primary intratesticular pleomorphic leiomyosarcoma: A rare case report

open access: yesIndian Journal of Pathology and Microbiology, 2013
Intratesticular leiomyosarcoma is an extremely rare tumor of the genitourinary system. We report a case of intratesticular pleomorphic leiomyosarcoma in a 68-year-old male who presented with gradual painless enlargement of the right scrotal mass over a ...
Rajshri Pisaram Damle   +3 more
doaj   +1 more source

“Pushing the margin:” utilization of renal autotransplantation to achieve complete resection in vena caval leiomyosarcomas

open access: yesJournal of Pediatric Surgery Case Reports, 2020
We report the case of a 19-year-old female who underwent resection of the sub- and infrahepatic inferior vena cava (IVC) with concomitant left kidney autotransplantation for leiomyosarcoma.
Joseph Anderson   +3 more
doaj   +1 more source

Renal Leiomyosarcoma

open access: yesRare Tumors, 2013
Leiomyosarcoma (LMS) is a rare malignant tumor of smooth muscle origin that generally stems from soft tissues and uterine tissue. Although, a small percentage of these may originate from the smooth muscle or vessel walls, most of which are of venous origin. Renal leiomyosarcomas may arise from the smooth muscle fibers of renal pelvis, renal capsule or
Pastora Beardo   +2 more
openaire   +3 more sources

Obstructive Small Bowel Metastasis from Uterine Leiomyosarcoma: A Case Report

open access: yesCase Reports in Obstetrics and Gynecology, 2014
Background. Uterine leiomyosarcoma is a rare and aggressive gynecologic malignancy with an overall poor prognosis. Lungs, bones, and brain are common sites of metastases of uterine leiomyosarcoma.
Mutahir A. Tunio   +5 more
doaj   +1 more source

Primary myxoid leiomyosarcoma of renal pelvis: Case report and literature review

open access: yesUrology Case Reports, 2022
Leiomyosarcoma arising from renal pelvis is a very rare disease. A patient was admitted to hospital with left renal colic due to nephrolithiasis, with a filling defect in renal pelvis that was considered to be a blood clot.
G.G. Krivoborodov   +5 more
doaj   +1 more source

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