Diagnostic Errors in Wilms' Tumors: Learning From Our Mistakes
Aim: This study aimed to analyze clinical characteristics and image findings in patients initially diagnosed with renal masses and treated on the Société Internationale d'Oncologie Pédiatrique (SIOP) 2001 protocol for Wilms tumor (WT) that eventually were diagnosed with different pathologies. M...
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Published in: | Frontiers in pediatrics Vol. 9; p. 757377 |
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Language: | English |
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Abstract | Aim:
This study aimed to analyze clinical characteristics and image findings in patients initially diagnosed with renal masses and treated on the Société Internationale d'Oncologie Pédiatrique (SIOP) 2001 protocol for Wilms tumor (WT) that eventually were diagnosed with different pathologies.
Methods:
We reviewed the preoperative symptoms, laboratory tests, and images of patients who were initially treated for WT and proved to have other diagnoses. Data from these patients were compared to those of the last 10 patients with WT and the last 10 patients with neuroblastoma (NBL) treated at a single institution.
Results:
From June 2001 to December 2020, we treated 299 patients with NBL and 194 with WT. Five patients treated with preoperative chemotherapy for WT were postoperatively diagnosed with NBL (one patient had bilateral renal masses and one with multifocal xanthogranulomatous pyelonephritis). Three underwent nephrectomy, two biopsies only, and one adrenalectomy due to intraoperative characteristics. Regarding clinical presentation, abdominal mass or swelling was very suggestive of WT (
p
= 0.011); pain, although very prevalent in the study group (67%), was not statistically significant, as well as intratumoral calcifications on computed tomography (CT) (67%). Urinary catecholamines were elevated in all patients mistreated for WT with the exception of the patient with pyelonephritis in which it was not collected.
Conclusion:
Some pathologies can be misdiagnosed as WT, especially when they present unspecified symptoms and dubious images. Diagnostic accuracy was 98.1%, which highlights the quality of the multidisciplinary team. Abdominal mass or swelling is highly suggestive of WT, especially in the absence of intratumoral calcifications on CT. If possible, urinary catecholamines should be collected at presentation as they help in the differential diagnosis of NBL. |
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AbstractList | Aim:
This study aimed to analyze clinical characteristics and image findings in patients initially diagnosed with renal masses and treated on the Société Internationale d'Oncologie Pédiatrique (SIOP) 2001 protocol for Wilms tumor (WT) that eventually were diagnosed with different pathologies.
Methods:
We reviewed the preoperative symptoms, laboratory tests, and images of patients who were initially treated for WT and proved to have other diagnoses. Data from these patients were compared to those of the last 10 patients with WT and the last 10 patients with neuroblastoma (NBL) treated at a single institution.
Results:
From June 2001 to December 2020, we treated 299 patients with NBL and 194 with WT. Five patients treated with preoperative chemotherapy for WT were postoperatively diagnosed with NBL (one patient had bilateral renal masses and one with multifocal xanthogranulomatous pyelonephritis). Three underwent nephrectomy, two biopsies only, and one adrenalectomy due to intraoperative characteristics. Regarding clinical presentation, abdominal mass or swelling was very suggestive of WT (
p
= 0.011); pain, although very prevalent in the study group (67%), was not statistically significant, as well as intratumoral calcifications on computed tomography (CT) (67%). Urinary catecholamines were elevated in all patients mistreated for WT with the exception of the patient with pyelonephritis in which it was not collected.
Conclusion:
Some pathologies can be misdiagnosed as WT, especially when they present unspecified symptoms and dubious images. Diagnostic accuracy was 98.1%, which highlights the quality of the multidisciplinary team. Abdominal mass or swelling is highly suggestive of WT, especially in the absence of intratumoral calcifications on CT. If possible, urinary catecholamines should be collected at presentation as they help in the differential diagnosis of NBL. Aim: This study aimed to analyze clinical characteristics and image findings in patients initially diagnosed with renal masses and treated on the Société Internationale d'Oncologie Pédiatrique (SIOP) 2001 protocol for Wilms tumor (WT) that eventually were diagnosed with different pathologies.Methods: We reviewed the preoperative symptoms, laboratory tests, and images of patients who were initially treated for WT and proved to have other diagnoses. Data from these patients were compared to those of the last 10 patients with WT and the last 10 patients with neuroblastoma (NBL) treated at a single institution.Results: From June 2001 to December 2020, we treated 299 patients with NBL and 194 with WT. Five patients treated with preoperative chemotherapy for WT were postoperatively diagnosed with NBL (one patient had bilateral renal masses and one with multifocal xanthogranulomatous pyelonephritis). Three underwent nephrectomy, two biopsies only, and one adrenalectomy due to intraoperative characteristics. Regarding clinical presentation, abdominal mass or swelling was very suggestive of WT (p = 0.011); pain, although very prevalent in the study group (67%), was not statistically significant, as well as intratumoral calcifications on computed tomography (CT) (67%). Urinary catecholamines were elevated in all patients mistreated for WT with the exception of the patient with pyelonephritis in which it was not collected.Conclusion: Some pathologies can be misdiagnosed as WT, especially when they present unspecified symptoms and dubious images. Diagnostic accuracy was 98.1%, which highlights the quality of the multidisciplinary team. Abdominal mass or swelling is highly suggestive of WT, especially in the absence of intratumoral calcifications on CT. If possible, urinary catecholamines should be collected at presentation as they help in the differential diagnosis of NBL. |
Author | Cypriano, Monica dos Santos Caran, Eliana Maria Monteiro Kobayashi, Thiago Lederman, Henrique Manoel Abib, Simone de Campos Vieira de Carvalho, Lucas Garschagen Alves, Maria Teresa de Seixas |
AuthorAffiliation | 1 Pediatric Oncology Institute, GRAACC Hospital, Federal University of São Paulo , São Paulo , Brazil 2 Paulista School of Medicine, Federal University of São Paulo , São Paulo , Brazil |
AuthorAffiliation_xml | – name: 1 Pediatric Oncology Institute, GRAACC Hospital, Federal University of São Paulo , São Paulo , Brazil – name: 2 Paulista School of Medicine, Federal University of São Paulo , São Paulo , Brazil |
Author_xml | – sequence: 1 givenname: Lucas Garschagen surname: de Carvalho fullname: de Carvalho, Lucas Garschagen – sequence: 2 givenname: Thiago surname: Kobayashi fullname: Kobayashi, Thiago – sequence: 3 givenname: Monica dos Santos surname: Cypriano fullname: Cypriano, Monica dos Santos – sequence: 4 givenname: Eliana Maria Monteiro surname: Caran fullname: Caran, Eliana Maria Monteiro – sequence: 5 givenname: Henrique Manoel surname: Lederman fullname: Lederman, Henrique Manoel – sequence: 6 givenname: Maria Teresa de Seixas surname: Alves fullname: Alves, Maria Teresa de Seixas – sequence: 7 givenname: Simone de Campos Vieira surname: Abib fullname: Abib, Simone de Campos Vieira |
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CitedBy_id | crossref_primary_10_1016_j_ncrna_2023_05_007 crossref_primary_10_3389_fped_2022_952989 crossref_primary_10_3390_children10111790 crossref_primary_10_4103_ipcares_ipcares_113_23 crossref_primary_10_4274_jpea_2024_254 crossref_primary_10_1007_s00117_023_01238_0 crossref_primary_10_1007_s00330_024_10589_8 crossref_primary_10_1016_j_prp_2024_155254 |
Cites_doi | 10.1016/j.jpedsurg.2008.02.077 10.1002/1097-0142(19950415)75:8<2186::AID-CNCR2820750825>3.0.CO;2-F 10.1038/nrc1014 10.1186/s12894-016-0155-5 10.1148/radiographics.4.6.915 10.1002/pbc.27627 10.1136/adc.87.3.241 10.1016/j.jpedsurg.2008.02.047 10.1097/MOP.0b013e32832b323a 10.1016/j.ejrad.2010.05.038 10.1007/s00247-007-0687-7 10.1148/radiographics.22.4.g02jl15911 10.1016/j.ucl.2004.04.014 10.32635/2176-9745.RBC.2005v51n4.1942 10.1002/mpo.10216 10.1200/JCO.1993.11.6.1014 10.1016/j.suc.2005.12.008 10.1102/1470-7330.2005.0104 |
ContentType | Journal Article |
Copyright | Copyright © 2021 de Carvalho, Kobayashi, Cypriano, Caran, Lederman, Alves and Abib. 2021 de Carvalho, Kobayashi, Cypriano, Caran, Lederman, Alves and Abib |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Pediatric Surgery, a section of the journal Frontiers in Pediatrics Reviewed by: Gloria Pelizzo, University of Milan, Italy; Hany Gabra, Newcastle Hospitals, United Kingdom Edited by: Luca Pio, Giannina Gaslini Institute (IRCCS), Italy |
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This study aimed to analyze clinical characteristics and image findings in patients initially diagnosed with renal masses and treated on the Société... Aim: This study aimed to analyze clinical characteristics and image findings in patients initially diagnosed with renal masses and treated on the Société... |
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SubjectTerms | diagnostic errors neuroblastoma Pediatrics preoperative chemotherapy surgery Wilms |
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Title | Diagnostic Errors in Wilms' Tumors: Learning From Our Mistakes |
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