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There is an emerging group of distinct vascular neoplasms with NFATC1/2 fusions, involving bones and soft tissues and often displaying focal epithelioid morphology, variable atypia of endothelial cells, predominantly vasoformative and in some cases focal solid growth. Although they may show aggressive local growth and may recur locally, malignant behaviour has not been documented. We present a case of a 35-year-old woman with multiple vascular neoplasms with a EWSR1::NFATC2 fusion involving the lungs, multiple bones (vertebra, femurs, tibia, pelvis) and probably the liver. The bone lesions were locally aggressive and recurred after surgical treatment. Nine years after the first manifestation, there was progression to an epithelioid angiosarcoma. The patient died 3 months after the diagnosis of epithelioid angiosarcoma with massive lung and liver involvement(metastases). In addition to the EWSR1::NFATC2 fusion, an activating PIK3CA gene mutation was identified in the angiosarcoma but not in the previously diagnosed bone tumours. To the best of our knowledge, this is the first documentation of malignant progression of a vascular neoplasm with NFATC1/2 fusion as well as visceral (lung) involvement.
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http://dx.doi.org/10.1007/s00428-024-03962-x | DOI Listing |
Front Oncol
August 2025
Department of Pathology, West China Hospital, Sichuan University, Chengdu, China.
In this study, we retrospectively analyzed the clinicopathological features of a case of hepatic infantile hemangioma (HIH) that malignantly transformed into hemangiosarcoma. HIH, a congenital disease, is the most common benign tumor of the liver in children, and its malignant transformation into hepatic angiosarcoma (HAS) is rare. HIH expresses markers of vascular origin and specifically expresses glucose transporter protein isoform 1.
View Article and Find Full Text PDFOral Oncol
September 2025
Department of Oral and Maxillofacial Pathology and Microbiology, Maulana Azad Institute of Dental Sciences, BSZ Marg, New Delhi 110002, India.
Epithelioid angiosarcoma is a rare and aggressive malignant neoplasm of endothelial origin, with limited cases reported in the oral cavity. Its clinical and histopathological features often mimic benign and malignant vascular lesions, posing a diagnostic challenge. The current case report is of a 42 year old male, who presented with a sessile granular growth with ulcerated surface on the palatal gingiva of one year duration.
View Article and Find Full Text PDFAm J Surg Pathol
July 2025
Institute of Pathology, University of Bonn, Germany.
Massive/mass-forming ductular reaction of the liver (MDR) is occasionally in the differential diagnosis with true bile duct tumors. Our diagnostic histomorphological and immunohistochemical study of 14 cases from a consultant collective of 2970 cases follows the appearance of MDR with regard to various underlying liver diseases and the conditions of pathologic perfusion. We describe MDR measuring up to 7 cm in localized form or affecting up to 70% of the parenchyma in subacute liver necrosis.
View Article and Find Full Text PDFJ Surg Case Rep
July 2025
Faculty of Medicine and Health, Northern Clinical School, University of Sydney, 1 Reserve Road, St Leonards, 2065, Sydney, Australia.
Polycystic liver disease (PLD) is an uncommon inherited condition that leads to progressive development of hepatic cysts that can become complicated by rupture, infection, and bleeding. We detail the case of a 53-year-old female presenting with haemoperitoneum secondary to hepatic cyst bleeding on a background of isolated polycystic liver disease. Despite extensive investigations to localize a bleeding source, repeated angioembolisation, and partial hepatic resection, the patient had recurrent hepatic haemorrhage.
View Article and Find Full Text PDFJ Gastrointest Surg
August 2025
Department of Gastrointestinal Surgery, Meizhou People's Hospital, Meizhou, Guangdong, China. Electronic address: