Erratum to “Erratum to “The SCARE guidelines: Consensus-based surgical case report guidelines” [Int. J. Surg. 34 (2016) 180–186]” [Int. J. Surg. 36 (2016) 396]

Agha, Riaz; Fowler, Alexander J.; Saeta, Alexandra; Barai, Ishani; Rajmohan, Shivanchan; Orgill, Dennis P.; Afifi, Raafat Yahia; Alahmadi, Raha; Albrecht, Joerg; Alsawadi, Abdulrahman; Aronson, Jeffrey K; Ather, M Hammad; Bashashati, Mohammad; Basu, Somprakas; Bradley, Patrick J.; Chalkoo, Mushtaq; Challacombe, Benjamin; Cross, Trent; Derbyshire, Laura; Farooq, Naheed; Hoffman, Jerome R.; Kadıoğlu, Hüseyin; Kasivisvanathan, Veeru; Kirshtein, Boris; Klappenbach, Roberto; Laskin, Daniel M.; Miguel, Diana; Milburn, James; Mousavi, Seyed Reza; Muensterer, Oliver J.; Ngu, James Chi Yong; Nixon, Iain J.; Noureldin, Ashraf; Perakath, Benjamin; Raison, Nicholas; Raveendran, Kandiah; Sullivan, Timothy; Thoma, Achilleas; Thorat, Mangesh A.; Valmasoni, Michele; Massarut, Samuele; D’Cruz, Anil; Vasudevan, Baskaran; Giordano, Salvatore; Roy, Gaurav; Healy, Donagh; Machado-Aranda, David; Carroll, Bryan T.; Rosin, David

doi:10.1016/j.ijsu.2017.08.568

Cited by 4 publications

(1 citation statement)

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“…This is the second GB case described in an adult patient >40-year-old suggesting that this type of neoplasm it is not age-related. Due to the rarity of this disease, the etiopathogenesis of this tumor is unclear, and it is believed to develop from a multipotent stem cell [9]. Likewise, the malignant potential and appropriate treatment for GB remains disputable [3].…”

Section: Discussionmentioning

confidence: 99%

Gastroblastoma in Adulthood—A Rarity among Rare Cancers—A Case Report and Review of the Literature

Centonze

Mangogna

Salviato

et al. 2019

Case Reports in Pathology

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Gastroblastoma (GB) is a rare gastric epithelial-mesenchymal neoplasm, first described by Miettinen et al. So far, all reported cases described the tumor in children or young adults, and similarities with other childhood blastomas have been postulated. We report a case of GB in a 43-year-old patient with long follow up and no recurrence up to 100 months after surgery. So far, this is the second case of GB occurring in the adult age >40-year-old. Hence, GB should be considered in the differential diagnosis of microscopically comparable conditions in adults carrying a worse prognosis and different clinical approach.

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Section: Discussionmentioning

confidence: 99%

Gastroblastoma in Adulthood—A Rarity among Rare Cancers—A Case Report and Review of the Literature

Centonze

Mangogna

Salviato

et al. 2019

Case Reports in Pathology

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Quadruple primary urogenital cancers – A case report

Elec¹,

Zaharie²,

Ene³

et al. 2017

International Journal of Surgery Case Reports

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Case Reports and Consent for Publishing in Rheumatology Journals

Pineda

Sandoval

2018

J Clin Rheumatol

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Case reports have a long-standing tradition in the current rheumatology literature. We aimed to present the main points of view regarding the importance, meaning, and barriers of consent for publishing under the comprehensive protection of patients' rights within this genre. We encourage Latin American editors and authors of rheumatology journals to adopt the best ethical practices in the field, avoiding security and legal liabilities from a regional perspective.

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Erratum to “Erratum to “The SCARE guidelines: Consensus-based surgical case report guidelines” [Int. J. Surg. 34 (2016) 180–186]” [Int. J. Surg. 36 (2016) 396]

Cited by 4 publications

References 1 publication

Gastroblastoma in Adulthood—A Rarity among Rare Cancers—A Case Report and Review of the Literature

Gastroblastoma in Adulthood—A Rarity among Rare Cancers—A Case Report and Review of the Literature

Quadruple primary urogenital cancers – A case report

Case Reports and Consent for Publishing in Rheumatology Journals

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