Results 91 to 100 of about 25,388 (210)
An unusual timing for symptomatic chest pain in an adult chest wall myofibroma: a case report [PDF]
, 2014 INTRODUCTION: Myofibromas are benign mesenchymal neoplasms that can present as solitary and multicentric lesions. They can occur in several locations and can occur at any age from neonates to elderly patients.
Chin-Li Chen, Hung Chang
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Melorheostosis: Clinical, radiological, and histopathological features with a literature review
Physiological Reports, Volume 13, Issue 21, November 2025.Abstract Melorheostosis is a rare sclerosing bone dysplasia that can clinically and radiologically mimic common bone disorders, particularly in atypical presentations. Its heterogeneous manifestations and limited awareness among clinicians frequently contribute to diagnostic delays or misdiagnosis. We report the case of a 34‐year‐old woman with chronic
Elif Koca +5 more
wiley +1 more source
Tumor fibroso solitario de la region parotidea: Reporte de un caso y revisión de la literatura [PDF]
, 2004 El tumor fibroso solitario es una entidad bien establecida, comúnmente localizada en la pleura, aunque recientemente se ha descrito en otras localizaciones, incluyendo la región de cabeza y cuello, en donde se presenta como una lesión bien circunscrita y
Granados García, Martín +3 more
core +1 more source
Mucoepidermoid carcinoma associated with osteosarcoma in a true malignant mixed tumor of the submandibular region [PDF]
, 2015 True malignant mixed tumor, also known as carcinosarcoma, is a rare tumor of the salivary gland composed of both malignant epithelial and malignant mesenchymal elements.
Cerbelli, B +4 more
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Genes, Chromosomes and Cancer, Volume 64, Issue 10, October 2025.ABSTRACT EWSR1::CREM fusion positive intrabdominal sarcomas defines a rare emerging group of aggressive mesenchymal neoplasms with a predilection for the celomic cavity and often manifesting perplexing immunophenotypic profile. There is no specific standard of care therapeutic option though anecdotal reports response to pazopanib have been reported. We
Saba Shafi +6 more
wiley +1 more source
Journal of Orthopaedic Surgery, 2005 Benign fibrous histiocytoma is such a rare tumour that only a few cases have been reported in the literature. A patient with an apparently benign lesion of the distal radius, along with congenital dislocation of the radial head, was presented at St. John'
S Sanatkumar +5 more
doaj +1 more source
A clinicohistopathological analysis of cutaneous fibrous histiocytomas of the finger
Indian Journal of Dermatology, 2020 Background: Cutaneous fibrous histiocytoma (CFH) is a common, benign skin tumor predominantly occurring on the extremities or trunk. However, CFH on the finger is rare. Objective: This study was undertaken to examine the clinicohistopathological features
Kyung-Hwa Nam +2 more
doaj +1 more source
Pediatric Blood &Cancer, Volume 72, Issue 10, October 2025.ABSTRACT Background Bone sarcomas other than osteosarcoma, chondrosarcoma, and Ewing sarcoma represent a challenge in care because they are uncommon, especially in children, adolescents, and young adults (AYA). Methods We conducted a retrospective review of patients aged 0–25 years treated for non‐osteosarcoma, non‐chondrosarcoma, non‐Ewing (and ...
Rafael Moisan +16 more
wiley +1 more source
Solitary fibrous tumour of the submandibular region: a rare entity [PDF]
, 2016 Solitary fibrous tumours of the head and neck region are extremely rare. The clinical diagnosis is often difficult to establish, and this lesion may be indistinguishable from other soft tissue neoplasms.
Ishak, Noor Liza +4 more
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Retroperitoneal liposarcoma : current insights in diagnosis and treatment [PDF]
, 2015 Retroperitoneal liposarcoma (RLS) are rare, biologically heterogeneous tumors that present considerable challenges due to their size and deep location. As a consequence, the majority of patients with high grade RLS will develop locally recurrent disease ...
Ceelen, Wim +2 more
core +3 more sources