Academic literature on the topic 'Wilms tumor; Child; CT scan'

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Journal articles on the topic "Wilms tumor; Child; CT scan"

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Ousmane, Traore, Kouma Alassane, Traore Fousseyni, et al. "CT in the prize in charge of wilms 'tumor (monocentric study of 13 cases)." World Journal of Biology Pharmacy and Health Sciences 6, no. 1 (2021): 054–60. https://doi.org/10.5281/zenodo.4767517.

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Nephroblastoma or Wilms tumor is a malignant tumor that develops at the expense of embryonic kidney tissue. It is the most common kidney tumor in children (> 90%); it represents around 5% to 14% of all childhood cancers. The aim of our work is to recall the contribution of imaging, in particular CT, in the management of this renal tumor. This is a retrospective, single-center study of 136 cases of Wilms tumors diagnosed in our clinic over a 2-year period. The mean age of the patients was 04 years with an extreme of (3 months -12 years) with a female prevalence (8 girls for 5 boys). Abdomina
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Tiwaskar, Suhas, and Charmy Rajesh Dhomne. "Case Report On Wilm's Tumor In Child." ECS Transactions 107, no. 1 (2022): 18985–90. http://dx.doi.org/10.1149/10701.18985ecst.

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Wilms tumor is the most frequent kind of kidney cancer in kids. It is responsible for around 6% of all tumors in children. In children under the age of 15, the incidence is 7.6 cases per million, with 75 percent of cases occurring before the child reaches the age of five. A variant term is nephroblastoma. It is most widespread between the ages of three and four, after which it becomes much less frequent. Clinical findings: Wilms tumor in children produces one or more of the following signs and symptoms: abdominal pain, increasing abdominal girth, lack of appetite, fever, blood in the urine, na
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Della Corte, Marcello, Elisa Cerchia, Marco Oderda, et al. "Prechemotherapy Transperitoneal Robotic-Assisted Partial Nephrectomy (RAPN) for a Wilms Tumor: Surgical and Oncological Outcomes in a Four-Year-Old Patient." Pediatric Reports 15, no. 3 (2023): 560–70. http://dx.doi.org/10.3390/pediatric15030051.

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Background: Wilms tumor (WT) is the most frequent renal tumor in children. The SIOP-UMBRELLA Guidelines allow for nephron-sparing surgery (NSS) in syndromic patients, as well as in cases of small (<300 mL) non-syndromic unilateral WTs, without lymph node involvement, and with a substantial expected remnant renal function, following neoadjuvant chemotherapy. We present a case of prechemotherapy transperitoneal robot-assisted partial nephrectomy (RAPN) for a unilateral, non-syndromic Wilms tumor. Methods: A four-year-old child presented with a solid mass measuring 3.6 cm in diameter involving
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Rehman, Fazal ur, Shakeel Ahmed, Waqas Ali, Asif Ali Khuhro, Sabiha Khan, and Basharat Hussain. "A rare case of Wilms Tumor in the right atrium." Professional Medical Journal 28, no. 06 (2021): 928–30. http://dx.doi.org/10.29309/tpmj/2021.28.06.6415.

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Improvement in outcome of Malignant solid tumor cases is credited to existence of well-defined guidelines and protocols and integrated treatment modalities involving chemotherapy, surgery and radiotherapy. The present case describes a rare case of Wilms tumor extending from the left kidney to left renal vein and then via inferior vena cava into the right atrium. This patients was 5 years of age and resident of Karachi presented to the outdoor of National Institute of Child Health (NICH) with the complaints of progressively increasing abdominal distension over the last two months that exacerbat
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Suwandy, Nicodemus, and Sri Mufti Ardani. "Tumor Wilms asimptomatik pada anak." Damianus Journal of Medicine 21, no. 3 (2022): 284–93. http://dx.doi.org/10.25170/djm.v21i3.3279.

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Pendahuluan: Tumor Wilms merupakan salah satu keganasan pada anak yang cukup sering ditemukan terutama pada anak usia di bawah 5 tahun. Seringkali tumor ini ditemukan secara kebetulan oleh orangtua ataupun pengasuh yang merasakan benjolan di perut anak. Kasus: Kami laporkan kasus tumor wilms pada anak usia 8 tahun yang ditemukan secara insidental. Pasien datang dengan keluhan nyeri perut kanan bawah disertai mual muntah dan demam, ditemukan nyeri tekan perut kanan bawah dan leukositosis. Kecurigaan awal mengarah ke apendisitis akut, namun pada pemeriksaan fisik juga ditemukan masa di abdomen k
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Rasool, Mumtaz, Mudassar Saeed Pansota, Fariha Mumtaz, Muhammad Shahzad Saleem, and Shafqat Ali Tabassum. "Positive predictive value (PPV) of computed tomography in diagnosing wilms’ tumor using histopathology as gold standard." Professional Medical Journal 26, no. 10 (2019): 1755–59. http://dx.doi.org/10.29309/tpmj/2019.26.10.4136.

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CT can also accurately identify vascular invasion that will impact surgical approach along with identification of the preoperative parameters associated with increased risk of intraoperative Wilms’ tumor spill. Objectives: To determine positive predictive value of CT scan in diagnosing wilm’s tumour, taking histopathology as gold standard. Study Design: Descriptive, cross sectional study. Setting: Department of Urology & Renal Transplantation Centre, Bahawal Vitoria Hospital, Bahawalpur. Period: From July 2017 to June 2018. Materials & Methods: A total of 81 patients with suspected wil
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Owens, C. M., P. A. Veys, J. Pritchard, G. Levitt, J. Imeson, and C. Dicks-Mireaux. "Role of Chest Computed Tomography at Diagnosis in the Management of Wilms’ Tumor: A Study by the United Kingdom Children’s Cancer Study Group." Journal of Clinical Oncology 20, no. 12 (2002): 2768–73. http://dx.doi.org/10.1200/jco.2002.02.147.

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PURPOSE: This study sought to determine whether the identification of minimal pulmonary metastatic disease by chest computed tomography (CT) performed at diagnosis in patients with Wilms’ tumor and normal chest x-rays (CXR) could predict a subgroup of children at increased risk of pulmonary relapse. PATIENTS AND METHODS: A retrospective analysis was carried out of the records of 449 children entered onto the United Kingdom Childrens’ Cancer Study Group Second Wilms’ Tumor Study between July 1986 and September 1991. The imaging protocol did not stipulate chest CT at diagnosis, but 141 children
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Green, D. M., D. J. Fernbach, P. Norkool, G. Kollia, and G. J. D'Angio. "The treatment of Wilms' tumor patients with pulmonary metastases detected only with computed tomography: a report from the National Wilms' Tumor Study." Journal of Clinical Oncology 9, no. 10 (1991): 1776–81. http://dx.doi.org/10.1200/jco.1991.9.10.1776.

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To evaluate the prognosis of patients with Wilms' tumor who have pulmonary densities identified on a computed tomographic (CT) scan of the chest, but have a negative plain chest radiograph, we reviewed the treatments and outcome of 32 patients randomized or followed on National Wilms' Tumor Study (NWTS)-3. The 4-year event-free and overall survival percentages of 18 of these patients who had a favorable histology tumor and were treated as stage IV tumors with three or four drugs plus whole-lung irradiation were 88.1% and 94.0%, respectively. The 4-year event-free and overall survival percentag
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Argani, Pedram, John P. Gearhart, Stanley S. Siegelman, and Naveen Subhas. "Nephrogenic rests mimicking Wilms' tumor on CT." Pediatric Radiology 34, no. 2 (2004): 152–55. http://dx.doi.org/10.1007/s00247-003-1008-4.

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Miazga, Małgorzata, Magdalena Ostojska, Wojciech Stręk, Marianna Maślana, Aleksandra Bogoń, and Magdalena Maria Woźniak. "Increasing abdominal circumference in children – does it require diagnosis?" Quality in Sport 15 (July 7, 2024): 52217. http://dx.doi.org/10.12775/qs.2024.15.52217.

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Introduction and purpose: Wilms tumor, also known as nephroblastoma, is the most prevalent malignant tumor of the kidney in the pediatric population. 90% of them are diagnosed in children before the age of 6. This tumor is more common in girls, and usually occurs unilaterally. The purpose of the study is to analyse and present the incidence of the patients with Wilms tumor in University Children’s Hospital in Lublin in comparison to other studies published on PubMed. Material and methods: The study included 34 patients with the Wilms tumor in the past medical history. They were selected among
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Conference papers on the topic "Wilms tumor; Child; CT scan"

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Oliveira, Emmanuelle Marie Albuquerque, Victor Regis de Lima, Lilian Balduíno de Menezes, Tatiane Kelly de Farias, and Rayle Maria Pereira da Silva. "Brain tumor in a pediatric patient with hydrocephalus: A case study." In II SEVEN INTERNATIONAL MEDICAL AND NURSING CONGRESS. Seven Congress, 2023. http://dx.doi.org/10.56238/iicongressmedicalnursing-012.

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This is a descriptive study, with a qualitative approach, of the case study type. The information contained in this chapter was obtained by reviewing the medical records, interviewing the patient and talking to medical and nursing professionals at the Hospital de Emergência e Trauma Dom Luiz Gonzaga Fernandes, located in Campina Grande, Paraíba. The patient L. S. F., female, 3 years old, born in Areial - PB, arrived at the Hospital presenting a convulsive crisis that lasted for 15 days, having a history of headache, vomiting, intermittent fever for more than 1 year. Upon admission, a CT scan o
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