Pancreatoblastoma: A report from the European cooperative study group for paediatric rare tumours (EXPeRT)

Bień, Ewa; Godziński, Jan; Dall’Igna, Patrizia; Defachelles, Anne‐Sophie; Stachowicz‐Stencel, Teresa; Orbach, Daniel; Bisogno, Gianni; Cecchetto, Giovanni; Warmann, Steven W.; Ellerkamp, Verena; Brennan, Bernadette; Balcerska, Anna; Rąpała, Małgorzata; Brecht, Ines B.; Schneider, Dominik; Ferrari, Andrea

doi:10.1016/j.ejca.2011.05.022

Cited by 101 publications

(142 citation statements)

References 19 publications

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“…To give an example, a first retrospective analysis has been published on pancreatoblastoma (20 cases collected over 10 years) [12]: despite the small number of cases, the study covers the largest series published to date and led to shared recommendations being developed for a standard approach to pancreatoblastoma, including a standardized diagnostic work-up, a prognostically relevant surgical staging system and a treatment protocol. Other analyses will shortly be published on such rare entities as ovarian Sertoli-Leydig cell tumors and pleuropulmonary blastoma.…”

Section: Editorialmentioning

confidence: 99%

The founding of the European Cooperative Study Group on Pediatric Rare Tumors – EXPeRT

Ferrari¹,

Schneider

Bisogno

et al. 2013

Expert Review of Anticancer Therapy

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Section: Editorialmentioning

confidence: 99%

The founding of the European Cooperative Study Group on Pediatric Rare Tumors – EXPeRT

Ferrari¹,

Schneider

Bisogno

et al. 2013

Expert Review of Anticancer Therapy

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“…55 The initial complete resection -primary and metastatic -correlates with longterm survival. 54,55 Solitary pseudopapillary neoplasms occur mostly in young female patients. Children present with symptoms, and the lesion is found in the head of the pancreas.…”

Section: Pediatric Pancreatic Surgerymentioning

confidence: 99%

“…Because these tumors secrete alphafetoproein, like hepatoblasoma, the treatment is with the same chemotherapeutic agents, and the response to therapy is similar. 55 This is administered as neo adjuvant therapy to highstage pancreatoblastoma to optimize a complete resection. 55 The initial complete resection -primary and metastatic -correlates with longterm survival.…”

Section: Pediatric Pancreatic Surgerymentioning

confidence: 99%

See 1 more Smart Citation

Whipple procedure: patient selection and special considerations

Tan-Tam¹,

Segedi²,

Chung³

2016

OAS

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At the inception of pancreatic surgery by Dr Whipple in 1930s, the mortality and morbidity risk was more than 20%. With further understanding of disease processes and improve ments in pancreas resection techniques, the mortality risk has decreased to less than 5%. Age and chronic illnesses are no longer a contraindication to surgical treatment. Life expectancy and quality of life at a later age have improved, making older patients more likely to receive pancreatic surgery, thereby also putting emphasis on operative patient selection to minimize complica tions. This review summarizes the benign and malignant illnesses that are treated with pancreas operations, and innovations and improvements in pancreatic surgery and perioperative care, and describes the careful selection process for patients who would benefit from an operation. These indications are not reserved only to Whipple operation, but to pancreatectomies as well.

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“…Полученные данные позволили авторам рекомендовать этот режим для неоперабельных опухолей [25]. После проведенной предоперационной химиотерапии, если удается выполнить радикальную операцию, результаты тоже можно считать удовлетворитель-ными [26].…”

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