Results 11 to 20 of about 2,219,836 (309)
Renal Primitive Neuroectodermal Tumor [PDF]
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 +2 more sources
Leiomyosarcoma of the Renal Vein That Enlarged Laterally While Preserving the Structure of the Renal Vein Lumen [PDF]
Introduction Primary renal vein leiomyosarcoma is an extremely rare disease and the tumor often infiltrates the vessel wall. We report a case of primary renal vein leiomyosarcoma that enlarged while preserving the structure of the renal vein lumen.
Naoki Tashiro +9 more
doaj +2 more sources
The International Society of Urological Pathology convened a consensus conference on renal cancer, preceded by an online survey, to address issues relating to the diagnosis and reporting of renal neoplasia. In this report, the role of biomarkers in the diagnosis and assessment of prognosis of renal tumors is addressed. In particular we focused upon the
Tan, Puay Hoon +146 more
openaire +8 more sources
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
Nefroma mesoblástico congénito: reporte de caso
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 +3 more
doaj +1 more source
Three-Dimensional Physical Model in Urologic Cancer
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 +5 more
doaj +1 more source
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 +8 more
doaj +1 more source
Renal leiomyoma: An uncommon differential diagnosis of renal masses in pediatric age
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 +5 more
doaj +1 more source
A case of primary renal oncocytic tumor: Chromophobe renal cell carcinoma or oncocytoma?
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 +5 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]
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 +39 more
core +1 more source

