Agreement between clinicoradiological signs at diagnosis and radiohistological analysis after neoadjuvant chemotherapy of suspected Wilms tumor rupture: Consequences on therapeutic choices

2019 ◽  
Vol 66 (6) ◽  
pp. e27674 ◽  
Author(s):  
Marie‐Amelyne Le Rouzic ◽  
Ludovic Mansuy ◽  
Marie‐Agnès Galloy ◽  
Jacqueline Champigneulle ◽  
Valérie Bernier ◽  
...  
Author(s):  
Ying Zhang ◽  
Hong-cheng Song ◽  
Yan-fang Yang ◽  
Ning Sun ◽  
Wei-ping Zhang ◽  
...  
Keyword(s):  

2016 ◽  
Vol 33 (1) ◽  
pp. 91-95 ◽  
Author(s):  
Hiroaki Fukuzawa ◽  
Yuko Shiima ◽  
Yasuhiko Mishima ◽  
Sachi Sekine ◽  
Shizu Miura ◽  
...  

Urology ◽  
2017 ◽  
Vol 100 ◽  
pp. 103-110 ◽  
Author(s):  
Roberto Iglesias Lopes ◽  
Jessica Ming ◽  
Martin A. Koyle ◽  
Ronald Grant ◽  
Adriana Fonseca ◽  
...  

2015 ◽  
Vol 37 (5) ◽  
pp. 396-401 ◽  
Author(s):  
Zhen Qin ◽  
Yiyun Tang ◽  
Hui Wang ◽  
Wei Cai ◽  
Hongliang Fu ◽  
...  

Children ◽  
2018 ◽  
Vol 5 (10) ◽  
pp. 134 ◽  
Author(s):  
Andrew Murphy ◽  
Andrew Davidoff

Historically, the management of bilateral Wilms tumor (BWT) was non-standardized and suffered from instances of prolonged chemotherapy and inconsistent surgical management which resulted in suboptimal renal and oncologic outcomes. Because of the risk of end-stage renal disease associated with the management of BWT, neoadjuvant chemotherapy and nephron-sparing surgery have been adopted as the guiding management principles. This management strategy balances acceptable oncologic outcomes against the risk of end-stage renal disease. A recent multi-institutional Children’s Oncology Group study (AREN0534) has confirmed the benefits of standardized 3-drug neoadjuvant chemotherapy and the utilization of nephron-sparing surgery in BWT patients; however, less than 50% of patients underwent bilateral nephron-sparing surgery. The coordination of neoadjuvant chemotherapy and the timing and implementation of bilateral nephron-sparing surgery are features of BWT management that require collaboration between oncologists and surgeons. This review discusses the surgical management strategy in the context of BWT disease biology, with an emphasis on timepoints during therapy at which surgical decision making can greatly impact this disease and minimize long-term toxicities.


2022 ◽  
pp. 000313482110707
Author(s):  
Katlyn G. McKay ◽  
Muhammad O. Abdul Ghani ◽  
Gabriella L. Crane ◽  
Parker T. Evans ◽  
Shilin Zhao ◽  
...  

Background The Children's Oncology Group recommends upfront resection of Wilms tumor (WT), however, unique scenarios warrant neoadjuvant chemotherapy and delayed resection. We hypothesized that in the context of neoadjuvant chemotherapy, minimally invasive surgery (MIS) to resect WT achieves equivalent oncologic fidelity and better maintains therapy schedules. Methods A retrospective analysis of WT treated between 2010-2021 at a free-standing children's hospital was performed. Patient and disease specific characteristics were collected, and pre-resection tumor volumes (TV) were calculated. Impact of MIS or open resection on oncologic fidelity and time to resume chemotherapy was analyzed. Results For the study period, 62 patients were treated for 65 WT, and 14 patients (22.6%) received neoadjuvant chemotherapy to treat 17 WT (26.2%): 7 Stage I (all predisposition syndromes), 2 stage III, 7 stage IV, and 1 stage V (bilateral). MIS was utilized to resect 6 WT from 5 patients. For partial nephrectomy, pre-resection TV was 0.38 ml if MIS and 10.38 ml if open ( P = .025). For radical nephrectomy, pre-resection TV was 31.58 ml if MIS and 175.00 ml if open ( P = .101). No significant differences between surgical approach were detected regarding pathologic variables or survival. Epidural use was significantly greater with open procedures ( P = .001). Length of stay was 2.00 days after MIS compared to 6.00 for open resection ( P = .004). Time to resume chemotherapy was 7.00 days after MIS versus 27.00 for open ( P = .004). Conclusion After neoadjuvant chemotherapy for WT, MIS partial and radical nephrectomies achieved equivalent oncologic fidelity, reduced epidural use and post-operative stays, and better maintained adjuvant therapy timelines when compared to open resections.


2019 ◽  
Vol 54 (4) ◽  
pp. 771-774 ◽  
Author(s):  
Seppo Taskinen ◽  
Outi Leskinen ◽  
Jouko Lohi ◽  
Minna Koskenvuo ◽  
Mervi Taskinen

2021 ◽  
Vol 20 (4) ◽  
pp. 276-279
Author(s):  
Rahul Gupta ◽  
Praveen Mathur ◽  
Vinayak S. Rengan ◽  
Gunjan Sharma ◽  
Punit Singh Parihar ◽  
...  

Cancer ◽  
2008 ◽  
Vol 113 (1) ◽  
pp. 202-213 ◽  
Author(s):  
Hervé J. Brisse ◽  
Gudrun Schleiermacher ◽  
Sabine Sarnacki ◽  
Sylvie Helfre ◽  
Pascale Philippe‐Chomette ◽  
...  
Keyword(s):  

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Abubakar Garba Farouk ◽  
H. A. Ibrahim ◽  
A. Farate ◽  
S. Wabada ◽  
M. G. Mustapha

Abstract Background Horseshoe kidney (HK) is one of the most common renal fusion abnormalities, with an incidence of 1:400 in the normal population. However, Wilms tumor (WT) arising in an HK is a rare occurrence. We report the case of a 9-year-old boy who presented with an advanced WT in an HK and also highlight the management challenges in a resource-poor setting such as ours. Case presentation The patient was a 9-year-old Nigerian boy presented to the Pediatrics Outpatient Clinic of the University of Maiduguri Teaching Hospital (UMTH) with a history of progressive abdominal swelling, weight loss, abdominal pain, and cough. Abdominal examination revealed an irregular, firm, and non-tender mass in the right lumbar region. A computed tomography (CT) scan of the abdomen showed a heterogeneously dense mass that was predominantly to the right side of the abdomen and crossed the midline to the left side, where it continued with the relatively normal renal tissue. Chest CT revealed pulmonary metastases. A diagnosis of WT in an HK was made. The patient had a 6-week course of neoadjuvant chemotherapy, and a right nephrectomy and left partial nephrectomy was performed. The final histologic diagnosis of WT was made. Radiotherapy was intended but was not available in our facility, and the parents could not afford referral to another center. Conclusions Children with a clinically suspected HK with WT should undergo a careful imaging evaluation such as CT before any surgical intervention. Neoadjuvant chemotherapy to reduce tumor bulk might be a good treatment method to reduce surgical morbidity and aid in complete excision and potential for preserving renal function.


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