Results 1 to 10 of about 2,219,170 (264)

Renal Primitive Neuroectodermal Tumor [PDF]

Journal 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, Ahmet Camtosun, İbrahim Dursun, Nusret Akpolat, İsmail Okan Yıldırım   +4 more
doaj   +2 more sources

Nefroma mesoblástico congénito: reporte de caso

Revista de la Facultad de Medicina Humana, 2022
El nefroma mesoblástico congénito (NMC), es el tumor renal más frecuente en recién nacidos e infantes menores de 3 meses. Se presenta el caso clínico de una paciente menor de 3 meses, con diagnóstico prenatal, referido de manera oportuna para evaluación
Carolina F. Paz Soldán Mesta, José L. Apaza León, Mariela Tello Pezo, Roxana M. Lipa Chancolla   +3 more
doaj   +1 more source

Three-Dimensional Physical Model in Urologic Cancer

Frontiers in Surgery, 2022
Three-dimensional (3D) printing, as an evolving technology, enables the creation of patient-specific physical models with high precision; thus, it is widely used in various clinical practices, especially urologic cancer.
Yu Xie, Yu Xie, Guanlin Wu, Yu Liang, Gang Fan, Gang Fan   +5 more
doaj   +1 more source

Tumor-to-tumor metastasis: an extremely rare combination with renal cell carcinoma as the donor and a pancreatic neuroendocrine tumor as the recipient

Surgical Case Reports, 2022
Background Tumor-to-tumor metastasis is a rare phenomenon in which primary tumor cells metastasize hematogenously into another tumor. Herein, we report an extremely rare case of a renal cell carcinoma metastasis into a pancreatic neuroendocrine tumor ...
Shunryo Minezaki, Takeyuki Misawa, Hiroyuki Tsukayama, Makoto Shibuya, Keita Wada, Keiji Sano, Makoto Mochizuki, Yuko Sasajima, Hiroshi Kondo   +8 more
doaj   +1 more source

Renal leiomyoma: An uncommon differential diagnosis of renal masses in pediatric age

Urology Case Reports, 2021
Leiomyoma is a mesenchymal tumor which arise from any structure or organ containing smooth muscle, but is frequently seen in the female genital tract. Renal leiomyoma is extremely rare benign lesion with low incidence (1:1000), has been reported mostly ...
Derya Karabulut, Aykut Alkan, Cihan Ozgur, Burak Gunay, Gulsah Burgazdere, Fulya Oz Puyan   +5 more
doaj   +1 more source

A case of primary renal oncocytic tumor: Chromophobe renal cell carcinoma or oncocytoma?

IJU Case Reports, 2023
Introduction “Other oncocytic renal tumors of the kidney” is a new category constituted by 2022 WHO classification and different in the point of morphology and immunohistochemistory from typical oncocytic/eosinophilic renal tumors including chromophobe ...
Kenta Matsui, Katsunori Uchida, Masahiro Kanai, Kana Asakawa, Miki Usui, Tetsuya Murata   +5 more
doaj   +1 more source

Neoadjuvant Nivolumab and Ipilimumab for Nonmetastatic Renal Cell Carcinoma with Tumor Thrombus [PDF]

Journal of Immunotherapy and Precision Oncology, 2023
Renal cell carcinoma with level IV tumor thrombus is a condition necessitating aggressive surgical management. Many solid organ malignancies often benefit from neoadjuvant treatments for tumor debulking and improvement of surgical outcomes.
Viraj A. Master, Benjamin N. Schmeusser, Adeboye O. Osunkoya, Arnold R. Palacios, Eric Midenberg, Lauren Yantorni, Kenneth Ogan, Mehmet A. Bilen   +7 more
doaj   +1 more source

UBE2QL1 is Disrupted by a Constitutional Translocation Associated with Renal Tumor Predisposition and is a Novel Candidate Renal Tumor Suppressor Gene [PDF]

, 2013
Investigation of rare familial forms of renal cell carcinoma (RCC) has led to the identification of genes such as VHL and MET that are also implicated in the pathogenesis of sporadic RCC. In order to identify a novel candidate renal tumor suppressor gene,
Hodgson, S, Morris, Mark R., Turnell, Andrew S., Woodward, ER, Prigmore, Elena, Woodward, Emma R.; id_orcid, Wake, NC, Wake, Naomi C., Gribble, Susan M., Ricketts, Christopher J., Skytte, AB, Brown, Michael, Banks, RE, Morris, MR, Prigmore, E, Maher, ER, Woodward, Emma R., Clarke, Noel, Hodgson, Shirley, Skytte, Anne-bine, Ricketts, CJ, Turnell, AS, Brown, Michael; id_orcid, Maher, Eamonn R., Clarke, N, Banks, Rosamonde E., Gribble, SM, Brown, M, Skytte, Anne Bine, Wake, N, Clarke, Noel W, Brown, Michael D, Ricketts, C, Woodward, E, Skytte, A-B, Maher, E, Morris, M, Banks, R, Turnell, A, Gribble, S   +39 more
core   +1 more source

Differential expression of prognostic proteomic markers in primary tumour, venous tumour thrombus and metastatic renal cell cancer tissue and correlation with patient outcome [PDF]

, 2013
Renal cell carcinoma (RCC) is the most deadly of urological malignancies. Metastatic disease affects one third of patients at diagnosis with a further third developing metastatic disease after extirpative surgery.
Antony C P Riddick, Stewart Grant D., Laird Alexander, Alexander Laird, Grant D Stewart, Laird, Alexander, O'Mahony, Fiach C, Riddick, Antony C P, Riddick Antony C. P., O’Mahony Fiach C., Harrison David J., Fiach C O'Mahony, Jyoti Nanda, Harrison, David J, David J Harrison, O'Mahony, Fiach C., Riddick, Antony C. P., Nanda Jyoti, Nanda, Jyoti, Stewart, Grant D., O’Donnell Marie, O'Donnell, Marie, Stewart, Grant D, Marie O'Donnell, Harrison, David J.   +24 more
core   +2 more sources

Dysembryoplastic Neuroepithelial Tumor: A Benign but Complex Tumor of the Cerebral Cortex [PDF]

, 2022
Dysembryoplastic neuroepithelial tumor (DNET) is a distinct type of low-grade glioneuronal tumor. Clinically, DNET is highly associated with intractable epilepsy in young children and adolescents.
김세훈
core   +1 more source