MALIGNANT NEOPLASMS AFTER TREATMENT FOR METACHRONOUS BILATERAL WILMS' TUMOR: A Literature Review

1999 ◽  
Vol 16 (6) ◽  
pp. 533-538 ◽  
Author(s):  
Arnold C. Paulino
2013 ◽  
Vol 30 (3) ◽  
pp. 318-320 ◽  
Author(s):  
Murat Alkan ◽  
Cemal Parlakgumus ◽  
Serdar Hilmi Iskit ◽  
Recep Tuncer ◽  
Hasan Okur ◽  
...  

Urology ◽  
2021 ◽  
Author(s):  
Deguang Meng ◽  
Xiaofeng Chang ◽  
Qinghua Ren ◽  
Jiatong Xu ◽  
Huanmin Wang

1987 ◽  
Vol 138 (4 Part 2) ◽  
pp. 968-973 ◽  
Author(s):  
M.L. Blute ◽  
P.P. Kelalis ◽  
K.P. Offord ◽  
N. Breslow ◽  
J.B. Beckwith ◽  
...  

2016 ◽  
Vol 12 (6) ◽  
pp. 5075-5079
Author(s):  
Zechen Yan ◽  
Qingjun Meng ◽  
Jinjian Yang ◽  
Junjie Zhang ◽  
Wei Zhao ◽  
...  

Author(s):  
Arnold C. Paulino ◽  
Judith Wilimas ◽  
Neyssa Marina ◽  
Dana Jones ◽  
Mahesh Kumar ◽  
...  

2009 ◽  
Vol 28 (5) ◽  
pp. 201-208 ◽  
Author(s):  
Mehar Chand Sharma ◽  
Deepali Jain ◽  
Chitra Sarkar ◽  
Veereshwar Bhatnagar ◽  
Arvind Rishi ◽  
...  

2021 ◽  
Author(s):  
Tommaso Panici Tonucci ◽  
Andrea Sironi ◽  
Eleonora Pisa ◽  
Benedetta Di Venosa ◽  
Luigi Bonavina

Summary Background Schwannoma is a benign tumor arising from Schwann cells of the peripheral nerves. It is often asymptomatic and can develop in the retroperitoneum, mediastinum, head and neck region, and upper and lower extremities. Schwannoma of the abdominal wall is extremely rare, but differential diagnosis with malignant neoplasms is important to reduce the risk of undertreatment. Methods A narrative review of abdominal wall schwannoma was performed using PubMed, EMBASE, and Web of Science database and the search terms “schwannoma”, “neurinoma”, “neurilemmoma”, “soft tissue tumors”, “neurogenic tumor”, “rectus abdominis mass”, “abdominal wall”. In addition, the hospital charts were reviewed to report the personal experience. Results Only 9 single case-reports of benign schwannoma of the abdominal wall were found in the English medical literature over the past decade. None of the patients received preoperative biopsy and all were resected with clear margins. In addition to the literature review, we report the case of a 58-year-old man referred for a palpable mass in the left upper abdominal quadrant. Ultrasonography and magnetic resonance imaging revealed a solid and well-encapsulated mass inside the left rectus abdominis muscle. A core biopsy of the lesion provided the diagnosis of cellular schwannoma and this was confirmed by histopathologic examination of the surgical specimen. Conclusions Benign schwannoma of the abdominal wall is extremely rare. Percutaneous core needle biopsy is important for the differential diagnosis with more common and biologically more aggressive malignancies, such as desmoid tumors and sarcomas, and may be relevant for planning the most appropriate management.


PEDIATRICS ◽  
1982 ◽  
Vol 70 (1) ◽  
pp. 135-136
Author(s):  
Deborah Tolchin ◽  
Mordecai Koenigsberg ◽  
Maria Santorineou

There have been many reports of the association between hemihypertrophy and intraabdominal masses, including Wilms' tumor, hepatoma, and adrenal cortical neoplasias.1 The present report describes a patient with segmental hemihypertrophy, multiple ovarian cysts, and bilateral Wilms' tumor and suggests a screening regimen for patients with hemihypertrophy. CASE REPORT The patient was a 9 lb 14 oz product of a term pregnancy, who was well until a mass filling the entire right side of the abdomen was discovered on routine examination at 4 months of age. Intravenous pyelogram (IVP) confirmed a large prerenal mass which on ultrasound was felt to be an ovarian cyst.


2018 ◽  
Vol 22 (3) ◽  
pp. 269-275 ◽  
Author(s):  
Alvin B Caballes ◽  
Agustina D Abelardo ◽  
Miguel J Farolan ◽  
Januario Antonio D Veloso

The case involves a 10-year-old child who underwent a left radical nephrectomy for what was believed to be a Wilms’ tumor. Histopath examination indicated a benign vascular lesion, subsequently determined to be an anastomosing hemangioma of the kidney. A comparison with the previously cited pediatric patients with renal vascular tumors is provided, and the inconsistent diagnostic terminologies for these conditions are highlighted. The therapeutic implications of these predominantly benign renal tumors, in the context of the much more frequently encountered malignant neoplasms in children, are additionally discussed.


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