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Journal articles on the topic 'Renal Tumors'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Khareba, G. G., V. M. Lisovyi, and D. V. Shchukin. "RESULTS OF NEPHRON-SPARING SURGERY OF INTRAPARENCHYMAL RENAL TUMORS." Актуальні проблеми сучасної медицини: Вісник Української медичної стоматологічної академії 20, no. 2 (2020): 96–101. http://dx.doi.org/10.31718/2077-1096.20.2.96.

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Surgical treatment is the main therapy for patients with renal cell carcinoma. The current approach in the treatment of kidney tumours has become widely introduced into nephron-sparing surgery. This approach is usually applied in cases of complex surgeries for large-size tumours with intravenous extension, multifocal, and intraparenchymal renal tumours. The purpose of the study was to investigate the results of nephron-sparing surgery for intraparenchymal renal tumours. Material and methods. The results were obtained in the process of nephron-sparing surgery treatment of 701 patients with rena

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2

Tan, Puay Hoon, Liang Cheng, Nathalie Rioux-Leclercq, et al. "Renal Tumors." American Journal of Surgical Pathology 37, no. 10 (2013): 1518–31. http://dx.doi.org/10.1097/pas.0b013e318299f12e.

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3

Peng, Sheng-Jeng. "Renal Tumors." Journal of Medical Ultrasound 23, no. 2 (2015): 65–66. http://dx.doi.org/10.1016/j.jmu.2015.03.005.

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4

Ruckle, Herbert C., Vicente E. Torres, Ronald L. Richardson, and Horst Zincke. "Renal tumors." Current Opinion in Nephrology and Hypertension 2, no. 2 (1993): 201–10. http://dx.doi.org/10.1097/00041552-199303000-00005.

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5

Miss., Surbhi Markam. "Tumors of Kidney." International Journal of Trend in Scientific Research and Development 3, no. 2 (2019): 663–71. https://doi.org/10.31142/ijtsrd21438.

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Kidney tumors, also known as renal tumors, are tumors, or growths, on or in the kidney. These growths can be benign or malignant cancerous . They may be discovered on medical imaging incidentally i.e. anincidentaloma , or may be present in patients as an abdominal mass, hematuria, abdominal pain, or manifest first in aparaneoplastic syndrome that seems unrelated to the kidney. The most common form of kidney cancer in adults is renal cell carcinoma. Renal cell carcinoma usually does not cause obvious symptoms, especially in the early stages. As a result, the cancer may not be discovered until i

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6

Kuznetsov, S. A., V. V. Sizonov, I. I. Belousov, and A. S. Podrezova. "Kidney cancer in a 14-year-old child: a rare clinical case description." Urology Herald 12, no. 6 (2025): 59–66. https://doi.org/10.21886/2308-6424-2024-12-6-59-66.

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Kidney tumours are among the most common solid malignant pathologies in children, accounting for 6 % of all childhood malignancies. About 89 % of these tumors are nephroblastomas (Wilms' tumors). Renal cell carcinoma in children is extremely rare, representing less than 1 % of all renal tumor pathologies in childhood and adolescence. Given the rarity of this pathology in children and the small size of neoplasms in the renal parenchyma, differential diagnosis between renal cancer and cystic renal lesions can be challenging. This clinical case describes a successful treatment case of a 14-year-o

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7

Sze, Sei-Gyung K. "Neonatal Renal Tumors." Clinics in Perinatology 48, no. 1 (2021): 71–81. http://dx.doi.org/10.1016/j.clp.2020.11.004.

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8

Süer, Evren, and Bilge Ayça Kırmızı. "Rare Renal Tumors." Üroonkoloji Bülteni 14, no. 3 (2015): 193–95. http://dx.doi.org/10.4274/uob.418.

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9

Herrera, Guillermo A. "Renal Tumors 2006." Pathology Case Reviews 11, no. 4 (2006): 153–55. http://dx.doi.org/10.1097/01.pcr.0000227454.04286.7d.

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10

Zöllner, S., U. Dirksen, H. Jürgens, and A. Ranft. "Renal Ewing tumors." Annals of Oncology 24, no. 9 (2013): 2455–61. http://dx.doi.org/10.1093/annonc/mdt215.

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11

Vasuri, Francesco, and Giovanni Fellegara. "Collision Renal Tumors." International Journal of Surgical Pathology 17, no. 4 (2008): 338–39. http://dx.doi.org/10.1177/1066896908321183.

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12

Lane, BrianR, George Jour, and Ming Zhou. "Renal neuroendocrine tumors." Indian Journal of Urology 25, no. 2 (2009): 155. http://dx.doi.org/10.4103/0970-1591.52905.

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13

Treece, Amy L. "Pediatric Renal Tumors." Surgical Pathology Clinics 13, no. 4 (2020): 695–718. http://dx.doi.org/10.1016/j.path.2020.08.003.

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14

Marshall, Fray F. "Editorial: Renal Tumors." Journal of Urology 152, no. 6 Part 1 (1994): 1992. http://dx.doi.org/10.1016/s0022-5347(17)32287-5.

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15

Zincke, Horst, and Michael L. Blute. "Editorial: Renal Tumors." Journal of Urology 152, no. 1 (1994): 43–44. http://dx.doi.org/10.1016/s0022-5347(17)32811-2.

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16

Pantuck, Allan J., Amnon Zisman, Mitchell K. Rauch, and Arie Belldegrun. "Incidental renal tumors." Urology 56, no. 2 (2000): 190–96. http://dx.doi.org/10.1016/s0090-4295(00)00655-5.

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17

Meilstrup, Jon W., Timothy J. Mosher, Rommel S. Dhadha, and David S. Hartman. "Other renal tumors." Seminars in Roentgenology 30, no. 2 (1995): 168–84. http://dx.doi.org/10.1016/s0037-198x(05)80032-x.

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18

Shamberger, Robert C. "Pediatric renal tumors." Seminars in Surgical Oncology 16, no. 2 (1999): 105–20. http://dx.doi.org/10.1002/(sici)1098-2388(199903)16:2<105::aid-ssu4>3.0.co;2-t.

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19

Fortich, Alejandra, Jose Gustavo Arrambide, and Victor David Ruiz. "Clinical case: renal tumor with succinate dehydrogenase deficiency during pregnancy." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 13, no. 11 (2024): 3323–26. http://dx.doi.org/10.18203/2320-1770.ijrcog20243198.

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Renal tumors during pregnancy present unique challenges due to the need to balance maternal and fetal health considerations. This case report describes a 31-year-old pregnant woman diagnosed with succinate dehydrogenase (SDH)-deficient renal cell carcinoma (RCC) during the second trimester. The patient presented with lumbar pain and hematuria, leading to the discovery of a left renal mass that was surgically removed via radical nephrectomy, with histopathological analysis confirming SDH-deficient RCC, stage 1. Postoperative care involved anticoagulation therapy, fetal heart rate monitoring and

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20

Austin, Publishing Group. "Primary Synovial Sarcoma of Kidney - A Histological Surprise: A Rare Case Report from a Tertiary Care Centre." Austin Journal of Clinical Case Reports 8, no. 10 (2021): 1234. https://doi.org/10.26420/austinjclincaserep.2021.1234.

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Abstract Renal Synovial Sarcoma (SS) are rare type of tumors arising from the mesenchymal tissue of the kidney. Its presenting features overlap with other renal tumors there by creating a diagnostic dilemma. Very few cases of primary renal SS are described so far in the literature with no defined treatment protocol described. We hereby describe a case report of this rare tumor in a 12 year old girl who presented to us with hematuria and flank pain. Histopathological analysis and the Immunohistochemistry (IHC) confirmed the diagnosis of primary monophasic synovial sarcoma. Follow-up post nephre

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21

Bartholow, Tanner, and Anil Parwani. "Renal Primitive Neuroectodermal Tumors." Archives of Pathology & Laboratory Medicine 136, no. 6 (2012): 686–90. http://dx.doi.org/10.5858/arpa.2011-0104-rs.

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Primitive neuroectodermal tumors exist as a part of the Ewing sarcoma/primitive neuroectodermal tumor family. These tumors most commonly arise in the chest wall and paraspinal regions; cases with a renal origin are rare entities, but have become increasingly reported in recent years. Although such cases occur across a wide age distribution, the average age for a patient with a renal primitive neuroectodermal tumor is the mid- to late 20s, with both males and females susceptible. Histologically, these tumors are characterized by pseudorosettes. Immunohistochemically, CD99 is an important diagno

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22

Mydlo, Jack H., Jeffrey Kaplan, William Thelmo, and Richard J. Macchia. "Spontaneous renal hemorrhage associated with renal tumors." Clinical Imaging 21, no. 4 (1997): 287–89. http://dx.doi.org/10.1016/s0899-7071(96)00079-4.

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23

Chen, You, Yuqing Shu, Laichang He, and Kaifu Wu. "Primary renal carcinoid tumors." Medicine 100, no. 8 (2021): e24714. http://dx.doi.org/10.1097/md.0000000000024714.

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24

Chughtai, Anila, Khadija Shafqat, Mohammad Fayyaz Anwar, and Akthar Sohail Chughtai. "Synchronous Ipsilateral Renal Tumors." Journal of the College of Physicians and Surgeons Pakistan 28, no. 6 (2018): S110—S111. http://dx.doi.org/10.29271/jcpsp.2018.06.s110.

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25

Schmidt, R., D. Stippel, T. Schmitz-Rixen, and M. Pollok. "Tumors after Renal Transplantation." Urologia Internationalis 57, no. 1 (1996): 21–26. http://dx.doi.org/10.1159/000282871.

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26

Herrera, Guillermo A., Mary Lowery-Nordberg, and Xin Gu. "Renal Epithelial Tumors 2006." Pathology Case Reviews 11, no. 4 (2006): 181–86. http://dx.doi.org/10.1097/01.pcr.0000227450.55200.89.

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27

Weeks, Douglas A., and Gary W. Mierau. "Renal Tumors of Childhood." Pathology Case Reviews 11, no. 4 (2006): 156–60. http://dx.doi.org/10.1097/01.pcr.0000227455.35590.90.

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28

Hes, Ondrej, Petr Kujal, Josef Sach, Petr Nencka, and Michal Michal. "Adult biphasic renal tumors." International Journal of Surgical Pathology 22, no. 5 (2014): 478–79. http://dx.doi.org/10.1177/1066896914525231.

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29

Kotagal, Meera, and James I. Geller. "Aggressive pediatric renal tumors." Seminars in Pediatric Surgery 28, no. 6 (2019): 150860. http://dx.doi.org/10.1016/j.sempedsurg.2019.150860.

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30

Truesdell, Mikki. "Cryoablation of Renal Tumors." Journal of Radiology Nursing 24, no. 2 (2005): 34. http://dx.doi.org/10.1016/j.jradnu.2005.04.010.

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31

Fernbach, Sandra K., and Kate A. Feinstein. "Renal tumors in children." Seminars in Roentgenology 30, no. 2 (1995): 200–217. http://dx.doi.org/10.1016/s0037-198x(05)80034-3.

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32

Lerner, Lori, and John Heaney. "Incidentally Detected Renal Tumors." Hospital Practice 32, no. 12 (1997): 53–65. http://dx.doi.org/10.1080/21548331.1997.11443607.

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33

Lee, Seong Wook. "Renal Tumors in Children." Clinical Pediatric Hematology-Oncology 24, no. 1 (2017): 21–36. http://dx.doi.org/10.15264/cpho.2017.24.1.21.

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34

Herts, Brian R. "Imaging for renal tumors." Current Opinion in Urology 13, no. 3 (2003): 181–86. http://dx.doi.org/10.1097/00042307-200305000-00002.

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35

Hélénon, O., J. Correas, C. Balleyguier, M. Ghouadni, and F. Cornud. "Ultrasound of renal tumors." European Radiology 11, no. 10 (2001): 1890–901. http://dx.doi.org/10.1007/s003300101077.

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36

Pivovarcikova, Kristyna, Reza Alaghehbandan, Tomas Vanecek, Riuko Ohashi, Tomas Pitra, and Ondrej Hes. "TSC/mTOR Pathway Mutation Associated Eosinophilic/Oncocytic Renal Neoplasms: A Heterogeneous Group of Tumors with Distinct Morphology, Immunohistochemical Profile, and Similar Genetic Background." Biomedicines 10, no. 2 (2022): 322. http://dx.doi.org/10.3390/biomedicines10020322.

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A number of recently described renal tumor entities share an eosinophilic/oncocytic morphology, somewhat solid architectural growth pattern, and tendency to present as low-stage tumors. The vast majority of such tumors follow a non-aggressive clinical behavior. In this review, we discuss the morphological, immunohistochemical, and molecular genetic profiles of the three most recent novel/emerging renal entities associated with TSC/mTOR pathway mutations. These are eosinophilic solid and cystic renal cell carcinoma, eosinophilic vacuolated tumors, and low-grade oncocytic tumors, which belong to

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37

Lee, Justin Scott, Thomas Ray Sanchez, and Sandra Wootton-Gorges. "Malignant renal tumors in children." Journal of Kidney Cancer and VHL 2, no. 3 (2015): 84–89. http://dx.doi.org/10.15586/jkcvhl.2015.29.

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Renal malignancies are common in children. While the majority of malignant renal masses are secondary to Wilms tumor, it can be challenging to distinguish from more aggressive renal masses. For suspicious renal lesions, it is crucial to ensure prompt diagnosis in order to select the appropriate surgical procedure and treatment. This review article will discuss the common differential diagnosis that can be encountered when evaluating a suspicious renal mass in the pediatric population. This includes clear cell sarcoma of the kidney, malignant rhabdoid tumor, renal medullary carcinoma and lympho

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38

Bakhshi, Girish D., Arshad S. Khan, Aftab S. Shaikh, Mohammad Ashraf A. Khan, Mohammad Adil A. Khan, and Nilofar M. Jamadar. "Primary renal synovial sarcoma." Clinics and Practice 2, no. 2 (2012): 44. http://dx.doi.org/10.4081/cp.2012.e44.

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Primary Renal Sarcoma is rare tumor comprising only 1% of all renal tumours. Synovial sarcomas are generally deep-seated tumors arising in the proximity of large joints of adolescents and young adults and account for 5-10% of all soft tissue tumours. Primary synovial sarcoma of kidney is rare and has poor prognosis. It can only be diagnosed by immunohistochemistry. It should be considered as a differential in sarcomatoid and spindle cell tumours. We present a case of 33-year-old female, who underwent left sided radical nephrectomy for renal tumour. Histopathology and genetic analysis diagnosed

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39

Vjestica, Jelena, Jasmina Markovic-Lipkovski, Cane Tulic, et al. "Pax-2 antigene expression in kidney tumours." Acta chirurgica Iugoslavica 58, no. 4 (2011): 15–20. http://dx.doi.org/10.2298/aci1104015v.

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Pax-2 transcriptional factor is expressed during kidney development and could re-express in renal tumors. The aim of this study was to examine Pax-2 expression in different types of renal cell carcinoma (RCC) in order to see whether it is good immunohistochemical marker. Method: We analyzed 48 different renal tumours stained with Pax-2 antibody. Pax-2 positive reaction was noticed in nucleus or cytoplasm. Expression of this antigen in tumours tissue was correlated with tumour stage and nuclear grade. Pax-2 expression between different histological RCC types was analyzed by X2 test and Fishers

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40

Karavaeva, E. A., T. E. Taranushenko, A. V. Morgun, et al. "Renal tumors in children and adolescents (primary diagnostics based on a pilot study)." Russian Journal of Woman and Child Health 4, no. 2 (2021): 162–67. http://dx.doi.org/10.32364/2618-8430-2021-4-2-162-167.

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Aim: to assess the rate of detection and epidemiology of renal tumors in children of the Krasnoyarsk Krai and to specify some tumor characteristics during primary diagnostics. Patients and Methods: retrospective exploratory (pilot) dynamic single-center study was conducted. A group of 46 children and adolescents with renal tumors who were admitted to the Department of Hematological Malignancies for examinations and treatment in 2011–2019. All data were obtained from hospital register. Results: renal tumors account for 6.4% of hematological malignancies first diagnosed in children. 9-year prima

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41

Singh, Madhuri, Shirish S. Chandanwale, Akshi Raj, Nayonikha Deokar, and Arpana Dharwadkar. "Histopathological Spectrum of Renal Tumors at a Tertiary Care Hospital." Asian Journal of Pharmaceutical Research and Health Care 17, no. 1 (2025): 14–19. https://doi.org/10.4103/ajprhc.ajprhc_9_24.

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Background: About 2%–3% of all adult malignancies diagnosed worldwide are renal cell carcinomas (RCCs), the most prevalent kind of renal malignancy. Renal tumors include a wide range of benign and malignant lesions, and the patterns of these lesions differ in adults and children. The most common renal tumor in childhood is Wilms tumor. Aim and Objective: The aim of this study was to examine different types of renal tumors, their incidence, and their histomorphological characteristics, as well as their relation to the patient’s age and sex. Results: During our study period of 2 years, 60 kidney

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42

Mukhopadhyay, Madhumita, Binata Bandopadhyay, Subhamoy Saha, and Biswanath Mukhopadhyay. "Rare Tumors of Kidney." International Journal of Research and Review 12, no. 2 (2025): 64–70. https://doi.org/10.52403/ijrr.20250208.

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INTRODUCTION: Collecting duct carcinoma (CDC) is an extremely rare type of renal epithelial tumor that arises from the distal convoluted tubule of kidney. Prognosis of CDC is poor due to its rapid growth and widespread metastasis. It is often difficult to distinguish CDC from pelvic urothelial carcinoma and high grade papillary Renal Cell Carcinoma. Mucinous tubular and spindle cell carcinoma (MTSCC) of kidney is also a rare but low grade epithelial neoplasm. It is often misdiagnosed as sarcomatoid renal cell carcinoma, papillary renal cell carcinoma or other aggressive renal neoplasms. MATERI

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43

Fischedick, A. R., P. E. Peters, G. Kleinhans, and E. Pfeifer. "Preoperative Renal Tumor Embolization." Acta Radiologica 28, no. 3 (1987): 303–6. http://dx.doi.org/10.1177/028418518702800315.

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The medical reports of 113 patients operated upon for renal tumors were retrospectively reviewed to assess the value of preoperative embolization. Coils or ethanol were used preoperatively in 55 patients while 58 patients underwent nephrectomy without embolization. The tumors were staged according to the TNM and the Robson staging classification. T1 and T2 tumors as well as T3 and T4 tumors were grouped together for statistical evaluation. There was no significant difference in intraoperative blood loss, operation time and survival rate between patients undergoing preoperative embolization and

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44

I*, Ziani. "Renal Epithelioid Angiomyolipoma: Diagnostic and Therapeutic Difficulty!" Open Access Journal of Urology & Nephrology 9, no. 4 (2024): 1–2. http://dx.doi.org/10.23880/oajun-16000263.

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Renal epithelioid angiomyolipomas (AMLeR) are rare tumors and account for 8% of angiomyolipomas (AML) operated ; We illustrate an observation of the diangotic and therapeutic difficulties of these types of tumors which remains rare, and whose management is not yet well defined both radiologically and urologically

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45

Wu, Pei-Yu, Sheng-Fung Lin, Ping-Hsun Wu, et al. "Multiple Hypovascular Tumors in Kidney: A Rare Case Report and Differential Diagnosis." Case Reports in Medicine 2013 (2013): 1–4. http://dx.doi.org/10.1155/2013/595193.

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The most common malignant renal tumor is renal cell carcinoma and surgery is the standard treatment. The proportion of lymphoma with renal involvement is 2~15% and lymphoma could be cured by chemotherapy without nephrectomy. Sonography, computed tomography (CT), and magnetic resonance imaging (MRI) can detect and characterize a renal mass. We present a case of right renal hypovascular tumors and differential diagnosis of hypovascular tumors by image study. CT scan showed hypovascular tumors and MRI image revealed multifocal hypovascular solid tumors with significantly increased apparent diffus

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46

Saber, Sadia, Paritosh Kumar Ghosh, Mohammed Tarek Alam, Naz Yasmin, Mohammad Monower Hossain, and Rafa Faaria Alam. "Atypical Presentation of Renal Cell Carcinoma: A Case Report." European Journal of Medical and Health Sciences 3, no. 1 (2021): 8–10. http://dx.doi.org/10.24018/ejmed.2021.3.1.650.

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The most common form of malignant renal tumours is Renal cell carcinoma (RCC) which is considered for nearly 80-85% of primary renal tumors. Now a day renal tumours can usually be detected at primary stage due to the popularity of sonography. Clinical manifestations of RCC have a diverse range. Loin pain, hematuria and abdominal mass contemplate as a classical triad but only present in 4–17% of cases. Here, we present a unique case of RCC in a 65 years old elderly gentleman admitted to our hospital with upper gastrointestinal (GI) symptoms without any significant GI involvement.

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47

Ingels, Alexandre, Eric Barret, Francois Audenet, et al. "Interest of percutaneous renal biopsy for small renal masses." Journal of Clinical Oncology 32, no. 4_suppl (2014): 539. http://dx.doi.org/10.1200/jco.2014.32.4_suppl.539.

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539 Background: Assess CT-scan guided renal biopsies relevance in the management of small renal masses. Methods: Retrospective analysis from 01/2007 to 12/2012 of percutaneous CT-scan guided renal biopsies performed at our institution for patients harboring renal tumors. Exclusion criteria were presence of metastasis and/or >4cm tumors. Data analyzed were pathological outcomes, management of the tumors and complications from the procedure during the 30 days post-biopsies. Results: 119 patients underwent a renal biopsy during this period. 79 presented the selection criteria. Renal biopsies l

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48

Seong, Chang Kyu, Seung Hyup Kim, Jong Seok Lee, Keon Ha Kim, Jung Suk Sim, and Kee-Hyun Chang. "Hypoechoic Normal Renal Sinus and Renal Pelvis Tumors." Journal of Ultrasound in Medicine 21, no. 9 (2002): 993–99. http://dx.doi.org/10.7863/jum.2002.21.9.993.

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49

Alaghehbandan, Reza, Delia Perez Montiel, Ana Silvia Luis, and Ondrej Hes. "Molecular Genetics of Renal Cell Tumors: A Practical Diagnostic Approach." Cancers 12, no. 1 (2019): 85. http://dx.doi.org/10.3390/cancers12010085.

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Renal epithelial cell tumors are composed of a heterogeneous group of tumors with variable morphologic, immunohistochemical, and molecular features. A “histo-molecular” approach is now an integral part of defining renal tumors, aiming to be clinically and therapeutically pertinent. Most renal epithelial tumors including the new and emerging entities have distinct molecular and genetic features which can be detected using various methods. Most renal epithelial tumors can be diagnosed easily based on pure histologic findings with or without immunohistochemical examination. Furthermore, molecular

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50

Monica, B., M. Zivieri, P. Cortellini, M. Simonazzi, and F. Poletti. "Papillary renal cell cystoadenocarcinoma." Urologia Journal 59, no. 1_suppl (1992): 211–13. http://dx.doi.org/10.1177/039156039205901s69.

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Papillary renal cell carcinoma (RCC) is known by the tendency to avascularity shown by angiography. More uncommon is the cystic variant of papillary RCC called cystoadenocarcinoma. The majority of papillary tumors are in stage I. The survival for papillary RCC is significantly higher than that for non-papillary RCC. CT-scan MNR, although non diagnostic, enhance the suspicion of a heterologous process in so called “complicated cysts”. US-guided percutaneous needle aspiration may be helpful to diagnose these tumours. We report 2 cases of cystodenocarcinoma and our considerations.

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