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Primary cardiac myxofibrosarcoma in a patient with Ebstein's anomaly: First reported case.
Int J Surg Case Rep
December 2024
Department of Pathology and Lab Medicine, Sri Aurobindo Medical College & Post Graduate Institute, Indore, India.
Article Synopsis
- Primary Cardiac Myxofibrosarcoma (PCM) is a rare and aggressive type of heart tumor, often asymptomatic and can be linked to congenital heart defects like Ebstein's anomaly.
- A case study presented a 38-year-old woman with Ebstein's anomaly who experienced breathing difficulties, leading to the discovery of a mobile cardiac mass that was ultimately diagnosed as PCM after surgical evaluation and histological analysis.
- The findings emphasize the importance of differentiating PCM from other cardiac masses through detailed pathological studies, as early detection and surgical intervention are crucial for improving outcomes in affected patients.
Soft tissue vascular tumor-like lesions in adults: imaging and pathological analysis pitfalls per ISSVA classification.
Insights Imaging
June 2024
Department of Radiology, Centre Hospitalier de l'Université de Montréal (CHUM), Montréal, QC, Canada.
Objectives: To compare the magnetic resonance imaging (MRI) and Doppler ultrasound (DUS) findings with the pathological findings of soft tissue vascular tumors (STVTs) according to the 2018 ISSVA (International Society for the Study of Vascular Anomalies) classification to differentiate vascular tumors from vascular malformations.
Methods: This retrospective study included patients with STVTs who underwent contrast-enhanced MRI and pathological analysis at our hospital between 2010 and 2020. The presumptive diagnosis based on the on-site imaging and histological analysis was compared with imaging and histological analysis conducted off-site utilizing the ISSVA criteria.
[Congenital spindle cell/sclerosing rhabdomyosarcoma: a clinicopathological analysis].
Zhonghua Bing Li Xue Za Zhi
April 2024
Department of Pathology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
To investigate the clinicopathological features, immunophenotype and molecular genetic characteristics of congenital spindle cell/sclerosing rhabdomyosarcoma. Sixteen cases (including 10 consultation cases) of congenital spindle cell/sclerosing rhabdomyosarcoma diagnosed at the Beijing Children's Hospital, Capital Medical University, Beijing China, from April 2017 to January 2022 were collected. These cases were evaluated for clinical profiles, histomorphological features, immunophenotype and molecular characteristics.
View Article and Find Full Text PDFMelanoma on congenital melanocytic nevi.
Pathol Res Pract
April 2024
University of Barcelona, Barcelona, Spain; August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Department of Dermatology, Hospital Clínic de Barcelona and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Spain. Electronic address:
Among nevus-associated melanomas, which overall account for 20%-30% of all melanomas, those arising specifically in congenital melanocytic nevi are infrequent, but can be disproportionately frequent in childhood and adolescence. Congenital melanocytic nevi (CMNi) are common benign melanocytic tumors that are present at birth or become apparent in early childhood. They are classified based on the projected adult size.
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