Year 2021 / Volume 113 / Number 5
Letter
Mucinous ascites secondary to peritoneal pseudomyxoma of an uncertain origin

380-381

DOI: 10.17235/reed.2020.7165/2020

Leire Parapar Álvarez, María Jesús Barragán González, Manuel Crespo Sánchez,

Abstract
Peritoneal pseudomyxoma (PP) is a rare malignant tumor, which is characterized by the presence of mucinous ascites. Abdominal ultrasound as the first diagnostic method of this entity allows the visualization of ascites on the one hand and its analysis through a diagnostic paracentesis on the other.
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References
1. Ioannidis O et al. Pseudomyxoma retroperitonei: report of 2 cases and review of the literature. Rev Esp Enferm Dig. 2012 May;104(5):268-75.
2. Pérez-Holanda S et al. Incidental pseudomyxoma peritonei of the appendix diagnosed by computed tomography with sagittal reconstruction in a woman suffering from postmenopausal metrorrhagia.Rev Esp Enferm Dig. 2009 Jul;101(7):510-2.
3. Gómez Portilla A et al. Pseudomyxoma peritonei. Over 10 years' survival after cytoreduction, intraperitoneal chemotherapy, and hyperthermia. Rev Esp Enferm Dig. 2008 Dic;100(12):806-7.
4. Funder JA, Jepsen KV, Stribolt K, Iversen LH. Palliative surgery for pseudomyxoma peritonei. Scand J Surg. 2016; 105 (2): 84-89.
5. Lord AC, Shihab O, Chandrakumaran K, Mohamed F, Cecil TD, Moran BJ. Recurrence and outcome after complete tumour removal and hyperthermic intraperitoneal chemotherapy in 512 patients with pseudomyxoma peritonei from perforated appendiceal mucinous tumours. Eur J Surg Oncol. 2015; 41 (3): 396-399
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Parapar Álvarez L, Barragán González M, Crespo Sánchez M. Mucinous ascites secondary to peritoneal pseudomyxoma of an uncertain origin. 7165/2020


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Publication history

Received: 19/04/2020

Accepted: 02/05/2020

Online First: 20/11/2020

Published: 10/05/2021

Article Online First time: 215 days

Article editing time: 386 days


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