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Around 2% of resected cardiac masses are ascribed to primary cardiac hemangiomas. With a variety of symptoms and variable natural history, these masses can be challenging to diagnose. This paper describes a case of a left ventricular mass in a young patient which was ultimately excised and diagnosed as a cavernous hemangioma.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11862176 | PMC |
http://dx.doi.org/10.1016/j.jaccas.2024.102956 | DOI Listing |
Front Oncol
August 2025
Department of Urology, The Second Hospital of Lanzhou University, Lanzhou, China.
Purpose: This study aimed to provide a case of scrotal hemangioma and examine its characteristics.
Methods: We presented a case report involving a sixteen-year-old male, detailing symptoms, physical examination, imaging studies, diagnosis, and treatment. We conducted a thorough literature analysis of case reports and examined their clinical characteristics, pathological categorization, recurrence, and complications.
Eye (Lond)
September 2025
Advanced Eye Centre, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Hepatobiliary Surg Nutr
August 2025
Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Folia Med (Plovdiv)
August 2025
St Anna University Hospital, Sofia, Bulgaria.
Tumors of the heart and blood vessels are relatively rare. Primary cardiac hemangiomas, in particular, are very rare benign tumors of the heart, occurring at a frequency of 2.8%.
View Article and Find Full Text PDFNeurogenetics
August 2025
Department of Human Genetics, University Medicine Greifswald and Interfaculty Institute of Genetics and Functional Genomics, University of Greifswald, Greifswald, Germany.
The detection of complex structural variants in patients with familial cerebral cavernous malformations (FCCM) remains challenging. Short-read whole genome sequencing was performed for a patient with strong clinical evidence of FCCM but negative results from previous genetic tests. The analysis revealed a large insertion of an intronic KRIT1 fragment into a coding exon of KRIT1.
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