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Darnis F, Fauvert RMésothéliome péritonéal malin diffus (ascite visqueuse Quinton A, Beylot J, Lebras MPéritonites gélatineuses (à propos de 2 cas). Dec 18, The main sign is abdominal ascites: from a simple effusion to an . La maladie gélatineuse du péritoine à propos d’un cas: médecine du. Jun 6, Request PDF on ResearchGate | La maladie gélatineuse du péritoine | Pseudomyxoma peritonei or gelatinous ascites is a rare clinical entity.

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Orphanet: Maladie gelatineuse du peritoine

Outline Masquer le plan. They are high in most of the patients and useful to survey the chemotherapy efficiency. Elles sont le plus souvent fines et curvilignes, plus rarement en amas fig.

Epithelial tumors Non-epithelial tumors Adenoma: J Ultrasound Med ; But, the main problem is the preitoine and post-surgical scarring, explaining imperatively a surgical and chemotherapeutic management at the same time.

The mesentery was normal and there were no lesions on ggelatineuse liver and stomach and omentum was normal macroscopically. Prognosis Pseudomyxoma peritonei is slowly progressive but recurrence after complete tumor removal may occur. It is a probable appendicular mucocele at the origin of this pseudomyxoma.

Group 3 consists of lesions of mucinous neoplasia of low grade, with or without cysts, characterized by a proliferation of cylindrical epithelial cells, flat or villous architecture with the presence of gelatiheuse, extraappendicular neoplastic cells, and absence of invasive extraappendicular focus.


Pseudomyxoma peritonei is characterized by disseminated intra-peritoneal mucinous tumors and mucinous ascites in the abdomen and pelvis.

The mainstay of the treatment is surgery and chemotherapy. Ann Surg TNM classification for mucinous peritoneal tumor: Am J Pathol ; Differential diagnosis The differential diagnosis includes secondary peritoneal carcinomatoses and other rare peritoneal tumors. During the procedure, it is possible to evacuate the mucus and wash the cavity, to perform the biopsies of the peritoneum, and to carry out a diagnostic adnexectomy, a systematic appendectomy.

Molecular genetic evidence supporting the clonality and appendiceal origin of pseudomyxoma peritonei in women. BM Ronnett, et al.

Health care resources for this disease Expert centres 66 Diagnostic tests 1 Patient organisations 26 Orphan drug s 0. The differential diagnosis revealed a stage III c ovarian cancer. The authors report a case of pseudomyxoma peritonei with gelatinous peritoneum in a year-old-woman. Click here to see the Library ]. This case was presented to the tumor board. Surgery must remove all lesions to eradicate the lesional process.

Dissemination initially is locoregional. Other search option s Alphabetical list.

Pseudomyxome péritonéal

Yelatineuse laparotomy remains a good method. World J Surg Oncol ;4: This article was submitted to Visceral Surgery, a section of the journal Frontiers in Surgery.


Computed tomography and sonography. Received Feb 14; Accepted Jul Ann Surg Oncol 4 A good washing of the peritoneal cavity is useful, but the recurrence is very frequent.

This examination shows a peritoneal pseudomyxoma with a partitioned mass encompassing the uterus and adnexa, nodular vesicular and tissue implants, and small mucoid implants scattered in the peritoneal cavity.

Multiple enteric bacteria are probably present in Qscite 6.

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Appendiceal mucocoeles and pseudomyxoma peritonei. In our case, washing and aspiration removed the maximum of the mucous effusion, and laparoscopy allowed us to visualize normal ovaries, but a bilateral biopsy was performed, and the systematic appendectomy diameter of the base of 1. Support Center Support Center. The tip is obstructed by a fibrous reshaping.

Author information Article notes Copyright and License information Disclaimer. The patient is not at a menopausal stage and had the last period date before a week of admission.

Clinical description The disease is usually diagnosed after the age of