Results 71 to 80 of about 8,902 (199)

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, Şeyhmus Kavak, Bilal Demir, Nil Comunoglu, Fatih Kantarci, Oguzhan Koca   +5 more
wiley   +1 more source

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
core   +2 more sources

Durable Response to Pazopanib (Tyrosine Kinase Inhibitor) in a Patient With EWSR1::CREM Gene Fusion Positive Intra‐Abdominal Unclassified Epithelioid Sarcoma

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, Dan Jones, Xiaokang Pan, Marium Husain, Alan Rogers, Steve Oghumu, O. Hans Iwenofu   +6 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, Meneses García, Abelardo, Ruíz Godoy Rivera, Luz María, Suárez Roa, María de Lourdes   +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, de Vincentiis, M, Iannella, G, Magliulo, G, Marcotullio, D   +4 more
core   +3 more sources

Benign Fibrous Histiocytoma of the Distal Radius with Congenital Dislocation of the Radial Head: A Case Report

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, N Rajagopalan, B Mallikarjunaswamy, S Srinivasalu, NP Sudhir, K Usha   +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, Sang-Woo Park, Seok-Kweon Yun   +2 more
doaj   +1 more source

Insights Into Non‐Classic Primary Bone Sarcomas in Children, Adolescents, and Young Adults: A French Descriptive Study

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, Jennifer Wallet, Sébastien Aubert, Pascaline Boudou‐Rouquette, Nathalie Gaspar, Perrine Marec‐Bérard, Estelle Thebaud, Emmanuelle Bompas, Gonzague de Pinieux, Jean‐Luc Jouve, Antoine Italiano, Christine Chevreau, Jean‐Yves Blay, Cyril Lervat, the GSF‐GETO, ResOs, and NETSARC+ networks   +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, Md Pauzi, Suria Hayati, Mohamad Yunus, Mohd Razif, Mohamed Rose, Isa, Sabir Husin Athar, Primuharsa Putra   +4 more
core  

A Young Man With Primary Pulmonary Myxoma

Clinical Case Reports, Volume 13, Issue 9, September 2025.
ABSTRACT Primary pulmonary myxoma is a rare tumor and is usually diagnosed incidentally in clinically asymptomatic patients as a well‐defined lung mass without metastasizing. It should also be considered that diagnostic methods such as bronchoscopy or transthoracic aspiration may be nondiagnostic.
Masoud Aliyali, Parnaz Rajabi, Gholamali Godazandeh, Siavash Abedi, Anahita Nosrati   +4 more
wiley   +1 more source