Results 61 to 70 of about 312,317 (298)

Mesenchymal Tumors of the Kidney in Adults

Kidney Cancer
Mesenchymal neoplasms of the kidney encompass a wide range of tumor types with heterogeneous clinical, histologic, and molecular features. Given their rarity relative to renal epithelial neoplasms, diagnosis may be challenging.
William J. Anderson
doaj   +1 more source

Isolated Renal Metastasis from Neuroendocrine Tumor: How Rare is Rare? A Case Report and Review of the Literature

Journal of Urological Surgery, 2016
Neuroendocrine tumors (NETs) are epithelial neoplasms arising from neuroendocrine cells that are widely distributed throughout the body. The kidney is a rare site for primary NETs and is even rarer as a metastatic site.
Irma Lengu, Santhi Ganesan
doaj   +1 more source

The Renal Tumor Morphological Characteristics that Affect Surgical Planning for Laparoscopic or Open Partial Nephrectomy [PDF]

, 2015
2015-02The purpose of this study is to investigate the morphological characteristics of renal tumors which affect the surgeons’ decision-making for the selection of open or laparoscopic partial nephrectomy.
YOSHINO, YASUSHI, MUROTANI, KENTA, ISHIDA, SHOHEI, SASSA, NAOTO, GOTOH, MOMOKAZU, FUNAHASHI, YASUHITO   +5 more
core   +1 more source

Navigating the complexity of Wilms tumors in pediatrics: diagnostic challenges for better treatment

Surgical and Experimental Pathology
Most pediatric kidney tumors clinically present as an abdominal mass, typically detected by the child’s caregivers and later confirmed through imaging tests.
Mariana Andozia Morini, Isabela Werneck da Cunha   +1 more
doaj   +1 more source

Fibrillary Glomerulonephritis and Multiple Myeloma: A Case Report and Literature Review

Case Reports in Oncology
Introduction: Fibrillary glomerulonephritis (FGN) is a rare form of immune complex-mediated primary glomerular disease frequently coexisting with malignancies or autoimmune diseases.
Taiki Ishida, Ken Morita, Yosuke Masamoto, Hideaki Mizuno, Kazuki Taoka, Hiroyuki Abe, Motoki Odawara, Yosuke Hirakawa, Masaomi Nangaku, Mineo Kurokawa   +9 more
doaj   +1 more source

Choroidal metastasis secondary to renal tumor

The Pan-American Journal of Ophthalmology, 2023
Renal tumors correspond to a small part of the total number of neoplasms. However, they can cause metastasis, mainly in the lungs, bones, and liver. In the eye, the uvea is the structure with the highest affinity due to its high vascularity, and its ...
Andres Felipe Ramirez Ossa, Sebastián Vallejo López, Diana Carolina Gómez Calle   +2 more
doaj   +1 more source

An epithelial GPR35 isoform supports tumor‐associated transcriptional and metabolic phenotypes

FEBS Letters, EarlyView.
GPR35 generates two functionally distinct isoforms with previously unresolved roles. GPR35‐short mediates immune‐cell chemotaxis, while GPR35‐long is enriched in colorectal cancer epithelium, where it supports increased metabolism, proliferation, and tumor‐associated transcriptional programs.
Jørgen D. Rønneberg, Martine Hjeltnes, Josephine Krieger, Joshua E. Elias, Maria Stensland, Kristian Holm, Xiaojun Jiang, Chuki Khangsar, Tuula A. Nyman, Arthur Kaser, Johannes R. Hov, Tom H. Karlsen, Nicole C. Kaneider, Frode L. Jahnsen, Georg Schneditz   +14 more
wiley   +1 more source

Neoplasms of the genitourinary system [PDF]

, 2018
Nephroblastoma or Wilms’ tumor (WT) is the most common renal neoplasm in children accounting for 90 % of pediatric renal tumors (Pastore et al. 2006). It is a tumor with a good prognosis and with well-established treatment strategies.
Smets, Anne, Hervé Brisse, Eline Deurloo, Anne Smets, Deurloo, Eline, Brisse, Hervé   +5 more
core   +1 more source

Primitive neuroectodermal tumor of the kidney: report of a patient

Acta Médica del Centro, 2012
Kidney neoplasms amount to 2-3% of total neoplasms; among them, primitive neuroectodermal tumors are not common. The case of a 28-year-old female patient, with a history of bronchial asthma, who went to see the doctor because she incidentally noticed an ...
Julio Vigil Quiñones, Paulino E. Hernández Hernández, Carmen Garrido Arce   +2 more
doaj  

The role of miR‐335‐5p in the redifferentiation of BRAF p.V600E thyroid cancers

Molecular Oncology, EarlyView.
The BRAF p.V600E mutation promotes thyroid cancer dedifferentiation and radioiodine resistance. Using a network approach, we identified miR‐335‐5p as a key regulator of BRAF‐mutated thyroid tumors. Restoring miR‐335‐5p increased thyroid‐specific gene expression and iodine uptake in cells and organoids.
Valeria Pecce, Simone Bini, Marialuisa Sponziello, Giorgio Grani, Giulia Fiscon, Paola Paci, Lorenzo Farina, Rosa Falcone, Valentina Maggisano, Sebastiano Filetti, Cosimo Durante, Antonella Verrienti   +11 more
wiley   +1 more source