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Infected psammomatous intracranial meningioma.
Neurochirurgie
January 2025
Department of Radiology, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris, INSERM U1148, Paris University, 46 rue Henri Huchard, 75018, Paris, France. Electronic address:
Case Report: Incidental discovery of primary peritoneal psammocarcinoma.
F1000Res
September 2024
Department of Pathology, Habib Thameur Hospital, Tunis, 1008, Tunisia.
Psammocarcinoma is an uncommon subtype of low-grade serous carcinoma. It is characterized by the presence of extensive psammoma bodies and can have either an ovarian or peritoneal origin. To our knowledge fewer than 30 cases of primary peritoneal psammocarcinoma (PPP) have been reported in the English literature.
View Article and Find Full Text PDFOmental calcified fibrous tumor with symptoms after COVID-19 infection.
J Surg Case Rep
March 2022
Department of Gastroenterology, İstinye University Liv Hospital, Istanbul, Turkey.
Calcified fibrous tumor (CFT) is a rare benign tumor of mesenchymal origin. Between 1988 and 2019, a total of 272 CFT cases were reported. CFTs can be seen in all anatomical regions with soft tissue.
View Article and Find Full Text PDFParaplegia due to spinal meningioma during the third trimester of pregnancy: case report and literature review.
Spinal Cord Ser Cases
April 2021
Clinical Epidemilogy, Anesthesiolgy, Cúcuta, Norte Santander, Colombia.
Introduction: Spinal meningiomas represent 25-45% of intradural spinal tumors and ~2% of meningiomas of the central nervous system (CNS), and their occurrence during pregnancy is unusual. We present an updated literature review.
Case Report: A 36-year-old woman, at 32.
Calcifying fibrous tumor of the terminal ileum mesentery: Case report.
Medicine (Baltimore)
December 2018
Landesklinikum Waidhofen an der Ybbs, Department of General Surgery.
Rationale: Calcifying fibrous tumors ("CFT") are recognized as extremely rare mesenchymal tumors with benign biological behavior and low rates of recurrence are seen after removal. The first case of a CFT was reported in 1988 as a possibly inflammatory triggered pseudotumor in deep soft tissue of children. Histologically, the tumor is typically composed of dense hyalinized collagen with paucicellular infiltration of lymphocytes and fibroblasts as well as psammomatous or dystrophic calcifications.
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