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Diagnostic radiologic features of pseudomyxoma peritonei consist of diffusely scattered plaques of calcifications in the abdomen, poorly defined soft tissue masses and ascites on plain abdominal radiographs, characteristic scalloping of the hepatic margin, numerous multilocular cystic masses with rims of curvilinear calcifications and compression of abdominal viscera without evidence of invasion at computed tomography, and an echogenic mantle with ascitic septations at ultrasonography. In an appropriate clinical setting, this spectrum of radiologic features is highly specific for the diagnosis of pseudomyxoma peritonei.
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http://dx.doi.org/10.1097/00004836-198606000-00024 | DOI Listing |
Cureus
February 2025
Department of Pathology, Antwerp University Hospital, Edegem, BEL.
Mucinous urachal neoplasms are rare and can present as benign cystadenomas, mucinous cystic tumors of low malignant potential (MCTLMPs), or invasive adenocarcinomas. MCTLMPs occupy a borderline category characterized by mild-to-moderate atypia and papillary/villous architecture without stromal invasion. Here, we describe a 54-year-old male patient who presented with persistent dysuria and was found to have a vesicourachal diverticulum.
View Article and Find Full Text PDFBMJ Case Rep
March 2025
Urology, All India Institute of Medical Sciences, New Delhi, Delhi, India.
A man in his 50s presented to the emergency department with a complaint of progressively increasing swelling in the lower abdomen. Investigations revealed a large pelvic mass for which a fine needle aspiration cytology was done, which was suggestive of adenocarcinoma. He was then referred to a urologist in view of suspected urachal adenocarcinoma.
View Article and Find Full Text PDFJ Pain Symptom Manage
March 2025
Department of Palliative medicine, Yamagata Prefectural Central Hospital, Yamagata, 990-2292, Japan. Electronic address:
Background: Nasogastric tube syndrome (NGTS) is a rare but potentially life-threatening complication of nasogastric tube (NGT) placement. It is characterized by throat pain, hoarseness, and vocal cord paralysis. Awareness is essential for preventing severe airway compromise.
View Article and Find Full Text PDFFront Genet
February 2025
Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, United States.
Introduction: Appendiceal mucinous neoplasms (AMN) are rare tumors of the gastrointestinal tract. They metastasize with widespread abdominal dissemination leading to pseudomyxoma peritonei (PMP), a disease with poor prognosis. There are many unknowns about the cellular features of origin, differentiation and progression of AMN and PMP.
View Article and Find Full Text PDFSurg Case Rep
February 2025
Department of Surgery, Erlangen University Hospital, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander-University Erlangen -Nuremberg (FAU), Erlangen, Germany.
Introduction: Localized cystic lymphangiomas (CL) are rare benign tumors deriving from the lymphatic system. CL is diagnosed more frequently in children than in the adult population and, although commonly affecting the cervical and axillary regions, can develop in various parts of the body. Abdominal cystic lymphangioma (ACL) comprises less than 5% of all CL cases.
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