Results 111 to 120 of about 39,428 (277)
Primary Angiosarcoma of the Mesentery: A Case Report
Angiosarcoma is a malignant endothelial cell tumor of lymphatic or vascular origin and is most commonly found in the skin and soft tissue. Primary mesenteric angiosarcoma has rarely been reported.
Hyeon Wook Kang +2 more
doaj +1 more source
Atypical Fibroxanthoma/Pleomorphic Dermal Sarcoma With Osseous Metaplasia: A Series of Three Cases
ABSTRACT Atypical fibroxanthoma (AFX) and pleomorphic dermal sarcoma (PDS) are rare mesenchymal tumors typically arising on sun‐damaged skin of the head and neck in elderly patients. PDS is a more aggressive tumor but with similar demographics, cellular morphology, immunohistochemical features, and genetic findings.
Taylor Novice +3 more
wiley +1 more source
Hepatic angiosarcoma with metastasis to small intestine [PDF]
Hepatic angiosarcomas are rare tumours with poor prognosis, with patients usually dying within 6 months. Metastases mainly occur in lymph nodes, spleen, lungs, bones and adrenals. Metastasis to small intestine is even rarer.
Ahmad, Zubair +5 more
core +1 more source
Despite cardiac metastases are found in about 20% of cancer deaths, the presence of primary cardiac tumors is rare. Most primary tumors are benign, and malignant tumors comprise about 15%. We report a 21-year-old man with fever, dyspnea, and hemoptysis that was diagnosed with angiosarcoma of the right atrium and pulmonary metastasis.
Monique Esteves Cardoso +4 more
openaire +3 more sources
CT Features of an Extraskeletal Osteosarcoma Associated With a Retained Surgical Sponge in a Dog
ABSTRACT An 8‐year‐old neutered female Labradoodle presented with acute restlessness and inability to stand. Point‐of‐care ultrasound revealed a large abdominal mass, prompting further imaging. Computed tomography (CT) demonstrated a mass with marked mineralization, a thick, enhancing rim, and signs of intra‐abdominal dissemination.
Kota Yamashita +3 more
wiley +1 more source
Epithelioid angiosarcoma revealed by livedoid distal vascular emboli
Angiosarcomas are rare malignant mesenchymal tumours with endothelial differentiation, which may arise in any organ. Angiosarcoma of the aorta is even more exceptional.
Annika Fournier, MD +6 more
doaj +1 more source
Angiosarcomas are rare but aggressive vascular cancers of endothelial cell origin. The diagnosis is often difficult, based on specific immunohistological features. They characteristically present a high local recurrence rate and an early metastatic potential.We report a case of angiosarcoma of the auricle in a 31-year-old female patient who presented ...
I, Barhmi +3 more
openaire +2 more sources
Pathogenic Neurofibromatosis type 1 gene variants in tumors of non‐NF1 patients and role of R1276
Somatic variants of the neurofibromatosis type 1 (NF1) gene occur across neoplasms without clinical manifestation of the disease NF1. We identified emerging somatic pathogenic NF1 variants and hotspots, for example, at the arginine finger 1276. Those missense variants provide fundamental information about neurofibromin's role in cancer.
Mareike Selig +7 more
wiley +1 more source
Violaceous nodules in an HIV-positive man [PDF]
Plasmablastic lymphoma (PBL) is a rare and aggressive malignancy associated with immunosuppression and the oncogenic effects of the Epstein-Barr virus (EBV).
Dominguez, Arturo R +2 more
core
Angiosarcoma of the breast, the unknown—a review of the current literature
Angiosarcoma of the breast is one of the rarest malignancies. Breast angiosarcoma can be classified into primary when arising de novo and secondary to chronic lymphoedema or breast irradiation. Molecular pathways involved in angiosarcoma development have
E. Esposito +13 more
semanticscholar +1 more source

