Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10988330 | PMC |
| http://dx.doi.org/10.1148/rycan.230198 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Calvarial Epithelioid Hemangioendothelioma Mimicking Osteosarcoma.
Radiol Imaging Cancer
March 2024
From the Department of Radiodiagnosis and Interventional Radiology, All India Institute of Medical Sciences, New Delhi, India (Y.S., A.G.); Department of Pathology, All India Institute of Medical Sciences, New Delhi, India (A.R.M.); and Department of Radiology, All India Institute of Medical Sciences, Dr. B. R. Ambedkar Institute Rotary Cancer Hospital, Rm No. 160D, Ansari Nagar, New Delhi 110029, India (K.R.).
Aggressive Cranial Osteoblastoma of the Parietotemporo-Occipital Bone: A Case Report and Review of Literature with Special Emphasis on Recurrence/Residue.
World Neurosurg
October 2020
Department of Neurosurgery, All India Institutes of Medical Sciences, New Delhi, India.
Osteoblastoma is a rare nonfibroblastic osteoid tissue-forming primary bony tumor usually arising in the medullary cavity/diploic space of any bone. The calvarium is an extremely rare site of its origin. Clinically, 2 types of osteoblastoma are noted: benign/conventional/typical and aggressive/high grade.
View Article and Find Full Text PDFRare Occurrence of an Intraocular Choroidal Solitary Fibrous Tumor/Hemangiopericytoma.
Ocul Oncol Pathol
June 2018
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Purpose: Tumors previously diagnosed as solitary fibrous tumors (SFT) and hemangiopericytomas (HPC) are characterized by the fusion gene, leading to nuclear STAT6 expression, and are now considered part of one SFT/HPC tumor entity by the 2016 World Health Organization Classification of Tumors of the Central Nervous System. We present the first primary choroidal SFT/HPC with the diagnosis confirmed by STAT6 expression.
Procedures: A 51-year-old man underwent enucleation for a choroidal mass, which revealed a spindle cell neoplasm involving the optic nerve, without extrascleral extension.
Recurrent atypical fibroxanthoma with satellite metastasis.
J Cutan Pathol
January 2015
Department of Pathology, University of Tennessee Graduate School of Medicine, Knoxville, TN, USA.
Atypical fibroxanthoma (AFX) is a cutaneous neoplasm of uncertain etiology that develops on sun-exposed regions of elderly males. It is widely considered to act indolently, despite its highly malignant cytologic features. Reports of metastatic AFX are very rare, and recurrence is uncommon.
View Article and Find Full Text PDFSclerosing epithelioid fibrosarcomas involving the neuraxis: report of three cases.
Neurosurgery
October 2000
Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Objective And Importance: Sclerosing epithelioid fibrosarcoma (SEF) is a rare mesenchymal neoplasm composed of rounded, vimentin-immunoreactive tumor cells disposed in nests and cords within a hyalinized collagenous matrix. Most examples arise in the deep skeletal muscles of adults. The cases recorded to date have been characterized by protracted clinical evolutions with a tendency for stubborn local recurrence, followed by late metastasis.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!