Cecal Volvulus following a Right Nephrectomy for Wilms' Tumor: Should We Need to Close the Lateral Peritoneum?

González-Urquijo, Mauricio; Ovalle-Chao, Christian; Flores‐Villalba, Eduardo; Garza-Luna, Ulises; Garza, Jose Humberto Velazco-De La; Garza-Serna, Ulises

doi:10.1055/s-0037-1612634

Cited by 4 publications

(4 citation statements)

References 20 publications

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“…W ilms' tumor is one of the most common malignant tumors in children, which is also known as embryonal tumor or renal embryonal tumor (Gonzalez-Urquijo et al, 2018;Guerreiro et al, 2018). In fact, Wilms' tumor is the high widespread solid tumors (Petiti et al, 2018).…”

Section: Introductionmentioning

confidence: 99%

Retracted: Long Noncoding RNA SOX2OT Accelerates the Carcinogenesis of Wilms' Tumor Through ceRNA Through miR-363/FOXP4 Axis

Sun

Kuai

et al. 2018

DNA and Cell Biology

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, are not of Wilms' tumor origin, but rather are Ewing (SK-NEP-1) (Memorial Sloan Kettering) and Rhabdoid (G-401) (ATCC). These data were provided by unimpeachable authorities. Memorial Sloan Kettering Cancer Center (among the premier institutions for cancer research in the world) and ATCC (the most highly respected repository for cell lines and reagents) disagree with the authors assumptions about the specificity of the origin of the cell lines. While many other publications can be found that assert the cell lines are of Wilms' tumor origin, this is not supported by the benchmark organizations. For that reason, the experimental conclusions drawn in this peer-reviewed paper cannot be attributed to provide insights into Wilms' tumors, but rather to two cell lines of other pedigree. Therefore, DNA and Cell Biology is officially retracting this paper.

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Section: Introductionmentioning

confidence: 99%

Retracted: Long Noncoding RNA SOX2OT Accelerates the Carcinogenesis of Wilms' Tumor Through ceRNA Through miR-363/FOXP4 Axis

Sun

Kuai

et al. 2018

DNA and Cell Biology

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“…In those above this age range, volvulus and intestinal malrotation can be mistaken for a range of conditions, such as pancreatitis, abdominal tuberculosis and gastro-oesophageal reflux, or even dismissed as a functional disorder [ 2 ]. This risk of misdiagnosis is exacerbated by an increased propensity for more atypical and chronic presentations of volvulus in the older population compared to those below the age of one [ 12 , 13 ]. Atypical presentations of volvulus most commonly include recurrent colicky abdominal pain and non-bilious vomiting [ 2 ].…”

Section: Discussionmentioning

confidence: 99%

‘Grumbling’ Midgut Volvulus in an Older Paediatric Patient With Congenital Solitary Kidney: A Case Report

Emmerson,

Dawson

2023

Cureus

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Midgut volvulus is a life-threatening condition, with the majority of cases presenting before the first year of life. Congenital gastrointestinal abnormalities can be associated with midgut volvulus; however, similar associations have not been described with congenital renal abnormalities. Congenital solitary kidney (CSK) means that a child is born with only one functional kidney. Here, we describe a case of a five-year-old child with CSK who atypically presents with midgut volvulus. The case highlights how midgut volvulus may present with chronic symptoms in those over the age of one and the importance of upper GI contrast studies for diagnosis of midgut volvulus in this population and suggests CSK along with other causes of solitary kidney as possible risk factors for volvulus.

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“…The diagnosis of CV can be challenging because the pattern of presentation varies from one patient to another and preoperative diagnosis is rarely achieved in most cases [4]. CV can also occur as a post-operative complication of certain surgeries like nephrectomy for Wilms' tumor [8]. However, this is an unusual complication because post-operative adhesions and intussusception have been reported as the most common causes of intestinal obstruction following nephrectomy [9].…”

Section: Discussionmentioning

confidence: 99%

Pediatric Cecal Volvulus: A Case Report

Emeka¹

2020

AJSCR

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Introduction: Cecal volvulus (CV) is rare cause of intestinal obstruction especially in children. There is no established protocol for the treatment of CV due to its rarity. Case Presentation: We present a rare case of CV in a 9-year-old girl. Discussion: The spectrum of intestinal malrotation may give rise to a mobile cecum that may result to CV. Constipation could be a predisposing factor. The clinical presentation which may include abdominal pain, distension, constipation and vomiting depends on the time of presentation. There may be associations with chromosomal abnormalities. Conclusion: Although CV is a rare cause of intestinal obstruction, awareness and high index of suspicion is needed by clinician for early diagnosis and treatment.

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Cecal Volvulus following a Right Nephrectomy for Wilms' Tumor: Should We Need to Close the Lateral Peritoneum?

Cited by 4 publications

References 20 publications

Retracted: Long Noncoding RNA SOX2OT Accelerates the Carcinogenesis of Wilms' Tumor Through ceRNA Through miR-363/FOXP4 Axis

Retracted: Long Noncoding RNA SOX2OT Accelerates the Carcinogenesis of Wilms' Tumor Through ceRNA Through miR-363/FOXP4 Axis

‘Grumbling’ Midgut Volvulus in an Older Paediatric Patient With Congenital Solitary Kidney: A Case Report

Pediatric Cecal Volvulus: A Case Report

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