The RENAPE observational registry: rationale and framework of the rare peritoneal tumors French patient registry

Author:

Villeneuve L., ,Passot G.,Glehen O.,Isaac S.,Bibeau F.,Rousset P.,Gilly F. N.

Funder

Institut National du Cancer (INCa)

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Reference58 articles.

1. Zhong Y, Deng M, Xu R, et al. Pseudomyxoma peritonei as an intractable disease and its preoperative assessment to help improve prognosis after surgery: a review of the literature. Intractable Rare Dis Res. 2012;1:115–21.

2. Smeenk RM, van Velthuysen ML, Verwaal VJ, Zoetmulder FA. Appendiceal neoplasms and pseudomyxoma peritonei: a population based study. Eur J Surg Oncol. 2008;34:196–201.

3. Sugarbaker PH, Ronnett BM, Archer A, et al. Pseudomyxoma peritonei syndrome. Adv Surg. 1996;30:233–80.

4. Mann Jr WJ, Wagner J, Chumas J, Chalas E. The management of pseudomyxoma peritonei. Cancer. 1990;66:1636–40.

5. Dartigues P, Isaac S, Villeneuve L, et al. Peritoneal pseudomyxoma: an overview emphasizing pathological assessment and therapeutic strategies. Ann Pathol. 2014;34:14–25.

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