Pseudomyxoma Peritonei Originating from an Intestinal Duplication
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چکیده
منابع مشابه
Pseudomyxoma Peritonei Originating from an Intestinal Duplication
Alimentary tract duplications are rare congenital anomalies. They most often become symptomatic in childhood and rarely undergo malignant transformation. Pseudomyxoma peritonei (PMP) is an equally uncommon condition, most frequently originating from a primary appendiceal mucinous neoplasm. We report an extremely unusual case of PMP arising from an intestinal duplication. A 67-year-old woman pre...
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Pseudomyxoma peritonei is a rare, slowly progressive disease that produces extensive mucus accumulation within the abdomen and pelvis. It is managed by cytoreductive surgery involving hyperthermic intraoperative intraperitoneal chemotherapy.
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Pseudomyxoma peritonei (PMP) is a rare clinical condition, where copious mucinous ascites accumulate in the peritoneal cavity due to dissemination of mucin-producing tumor. Because of this disseminating, yet nonmetastasizing, behavior, PMP attracts much interest from surgical oncologists in that aggressive locoregional therapy can give the opportunity of long survival and even cure. Although ex...
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Pseudomyxoma peritonei is a relatively rare and poorly understood condition in which mucus accumulates within the peritoneal cavity. The presence of cells in the mucin, either inflammatory or neoplastic, distinguishes it from simple acellular mucus ascites caused by mucinous spillage. There is widespread seeding of the peritoneal and omental surfaces with a heavy cancerous glaze. This is princi...
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THE PATIENT WAS a 71-year-old man admitted for the evaluation of an asymptomatic 7-cm thoracic aortic aneurysm. On physical examination, he was noted to have abdominal ascites. A computed tomography scan of the abdomen showed intra-abdominal heterogeneous mucinous material with scalloping of the liver, spleen, and mesentery. The patient underwent a diagnostic laparoscopy that revealed a large a...
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ژورنال
عنوان ژورنال: Case Reports in Pathology
سال: 2013
ISSN: 2090-6781,2090-679X
DOI: 10.1155/2013/608016