Results 11 to 20 of about 721,252 (305)

Renal carcinoid tumor

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2009
Primary renal carcinoid is a rare tumor, until now less than 50 cases of this tumor has been reported, so very little is known about its presentation clinicopathologic patterns and prognosis.
Geramizadeh Bita   +2 more
doaj   +2 more sources

Tumor renal

open access: yesMedisur, 2016
Yarisdey Corrales Hernández   +1 more
doaj   +3 more sources

Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies [PDF]

open access: yes, 2019
A significantly increased level of the reactive oxygen species (ROS) scavenger glutathione (GSH) has been identified as a hallmark of renal cell carcinoma (RCC). The proposed mechanism for increased GSH levels is to counteract damaging ROS to sustain the
Meierhofer, David, Xiao, Yi
core   +2 more sources

The ambitious role of anti angiogenesis molecules: Turning a cold tumor into a hot one [PDF]

open access: yes, 2018
In renal cancer emerging treatment options are becoming available and there is a strong need to combine therapies to reformulate and adjourn clinical practice.
Botticelli, A.   +4 more
core   +1 more source

A Rare Case of Neuroendocrine Tumor Following Radical Nephrectomy

open access: yesFolia Medica Indonesiana, 2022
Highlights: • Rare occurrence of a large, well-differentiated primary renal neuroendocrine tumor in a young man. • Identifying primary renal NET from the workup and histological examination of renal tumors needs to be done to understand more of this ...
Muhammad Rozaqy Ishaq   +2 more
doaj   +1 more source

Targeting hypoxia-inducible factor-1α (HIF-1α) in combination with antiangiogenic therapy: a phase I trial of bortezomib plus bevacizumab. [PDF]

open access: yes, 2014
PurposeWe hypothesized that bortezomib, an agent that suppresses HIF-1α transcriptional activity, when combined with bevacizumab, would obviate the HIF-1α resistance pathway.
Amin, Hesham M   +16 more
core   +2 more sources

Nefroma mesoblastico congénito: reporte de un caso

open access: yesGaceta Médica Boliviana, 2021
El nefroma mesoblastico congénito es un tumor renal infrecuente, pero común en el periodo neonatal. De comportamiento benigno y pronóstico excelente en su variedad clásica pero en el subtipo celular puede presentar recurrencia local, invasión ...
Lorena Arze Aimaretti   +5 more
doaj  

Renal myxoma – a case report of a rare kidney tumor, its differential diagnosis and literature review

open access: yesIJU Case Reports, 2022
Introduction Myxoma is a rare benign kidney tumor. Only 18 cases have been described in the literature. We report a new case of renal myxoma that arises from the renal parenchyma. Case presentation A 56‐year‐old man, medically free, presented complaining
Rawan Hudairy   +5 more
doaj   +1 more source

Renal Primitive Neuroectodermal Tumor

open access: yesJournal of Urological Surgery, 2017
Renal primitive neuroectodermal tumor (PNET) is a rare entity and highly malignant neoplasm. It generally occurs in young adults and children. We report a case of 19-year-old female with the complaint of left flank pain. Ultrasonography showed a tumor of
Hüseyin Çelik   +4 more
doaj   +1 more source

Renal neuroendocrine tumors

open access: yesIndian Journal of Urology, 2009
Neuroendocrine tumors (NETs) are uncommon tumors that exhibit a wide range of neuroendocrine differentiation and biological behavior. Primary NETs of the kidney, including carcinoid tumor, small cell carcinoma (SCC), and large cell neuroendocrine carcinoma (LCNEC) are exceedingly rare.The clinicopathologic features of renal NETs diagnosed at a single ...
Brian R Lane, George Jour, Ming Zhou
openaire   +3 more sources

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