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Soft Tissue Neoplasms (Fat, Muscle) [PDF]

, 2013
Clinical: Asymptomatic, solitary, slow-growing, rubbery, mobile subcutaneous nodules usually
Martin C. Mihm, Cary Chisholm, Chad Jessup, Clay J. Cockerell, Margaret Merola, Brian J. Hall   +5 more
openaire   +2 more sources

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CT of soft-tissue neoplasms

American Journal of Roentgenology, 1985
The computed tomographic scans (CT) of 84 patients with untreated soft-tissue neoplasms were studied, 75 with primary and nine with secondary lesions. Each scan was evaluated using several criteria: homogeneity and density, presence and type of calcification, presence of bony destruction, involvement of multiple muscle groups, definition of adjacent ...
HM Reiman, DJ Pritchard, Richard A. McLeod, RG Weekes   +3 more
openaire   +4 more sources

Mimics of Bone and Soft Tissue Neoplasms

Radiologic Clinics of North America, 2011
Many benign nonneoplastic entities can mimic bone and soft tissue tumors on imaging examinations. Distinguishing between neoplastic and nonneoplastic entities depends on history and physical examination findings and imaging findings, and is an important early step in the patient's overall workup and treatment plan.
G. Scott Stacy, Avnit Kapur
openaire   +4 more sources

Sox10 and S100 in the Diagnosis of Soft-tissue Neoplasms

Applied Immunohistochemistry & Molecular Morphology, 2012
Despite a well-characterized lack of specificity, pathologists routinely employ S100 in the diagnosis of neural crest-derived tumors. Recent studies have shown that Sox10 is a reliable marker of neural crest differentiation that is consistently expressed in schwannian and melanocytic tumors.
Matt van de Rijn, Robert B. West, Jason Karamchandani, Torsten O. Nielsen   +3 more
openaire   +3 more sources

Distinctive Head and Neck Bone and Soft Tissue Neoplasms

Surgical Pathology Clinics, 2017
Benign and malignant primary bone and soft tissue lesions of the head and neck are rare. The uncommon nature of these tumors, combined with the complex anatomy of the head and neck, pose diagnostic challenges to pathologists. This article describes the pertinent clinical, radiographic, and pathologic features of selected bone and soft tissue tumors ...
Chi K. Lai, Bibianna Purgina
openaire   +3 more sources

Soft-Tissue Neoplasms Associated with Congenital Neurofibromatosis

The Journal of Bone & Joint Surgery, 1956
Soft-tissue neoplasms are not infrequently encountered as one of the clinical manifestations of congenital neurofibromatosis. In those patients in whom diffuse soft-tissue hypertrophy remains relatively isolated and in whom it is limited to a portion of one extremity, radical excision of the hypertrophied subcutaneous tissue and the involved peripheral
H. Mccarroll
openaire   +4 more sources

Undifferentiated and dedifferentiated soft tissue neoplasms: Immunohistochemical surrogates for differential diagnosis.

Seminars in diagnostic pathology, 2021
Undifferentiated soft tissue sarcomas (USTS) are described in the current World Health Organization Classification of Soft Tissue and Bone Tumours as those showing no identifiable line of differentiation when analyzed by presently available technologies.
K. Thway, C. Fisher
semanticscholar   +1 more source

Clinicopathological and molecular characterisation of USP6‐rearranged soft tissue neoplasms: the evidence of genetic relatedness indicates an expanding family with variable bone‐forming capacity

Histopathology, 2020
USP6 rearrangement underpins self‐limiting fibroblastic/myofibroblastic neoplasms, including nodular fasciitis (NF), myositis ossificans (MO), aneurysmal bone cyst (ABC), and related variants.
Jui‐Chu Wang, Wan-Shan Li, Yu-Chien Kao, Jen-Chieh Lee, Pei-Hang Lee, Shih-Chiang Huang, Jen‐Wei Tsai, Chien-Chin Chen, Ching-Di Chang, Shih‐Chen Yu, Hsuan-Ying Huang   +10 more
semanticscholar   +1 more source