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Rare adrenal anastomosing hemangioma coexisting with adrenal cortical nodular hyperplasia: A case report.
Asian J Surg
November 2024
The Department of Urology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, PR China. Electronic address:
Anastomosing hemangioma of the kidney: A rare case report.
Int J Surg Case Rep
November 2024
Department of Pathology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India. Electronic address:
Article Synopsis
- Hemangiomas are benign vascular tumors that primarily affect the skin and soft tissues, with anastomosing hemangioma (AH) being a specific subtype that mimics more serious conditions like angiosarcoma; there are fewer than 300 reported cases of renal hemangiomas.
- A case study of a 28-year-old male revealed a left renal mass identified during tests for abdominal pain, with subsequent imaging and surgery confirming the diagnosis of AH through histopathological analysis and specific immunohistochemical markers.
- Accurate diagnosis of AH is crucial to avoid unnecessary treatment and complications, highlighting the need for greater awareness and reporting in the medical community to enhance diagnostic accuracy and patient management.
Clinical characteristics of renal anastomotic hemangioma.
World J Clin Cases
October 2024
Department of Urology, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou 225001, Jiangsu Province, China.
In this editorial, we comment on the article by Chen and Cai. We focus on renal anastomotic hemangioma, which is a rare benign hemangiomatous disease. This disease has unique clinical characteristics.
View Article and Find Full Text PDFIntramuscular hemangioma capillary type with HRAS mutation: Expanding the molecular genetic spectrum with an emphasis on overlap with arteriovenous malformations and distinct from infantile hemangioma.
Hum Pathol
November 2024
Department of Pathology, Henan Provincial People's Hospital, the People's Hospital of Zhengzhou University, Zhengzhou, China. Electronic address:
Article Synopsis
- Intramuscular hemangioma capillary type (IHCT) is a rare, fast-flow vascular lesion characterized by painless masses that commonly affect young adults and can involve various body locations, including the trunk and extremities.
- The study analyzed ten surgically treated IHCT cases from a pathology database and identified significant histopathological features, such as capillary-type vessels, and detected various somatic mutations, particularly in the MAP2K1 and KRAS genes.
- The findings suggest that IHCT shares genetic and hemodynamic similarities with arteriovenous malformations (AVMs), indicating potential new genetic targets for treatment development.
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