Results 101 to 110 of about 25,388 (210)

A Young Man With Primary Pulmonary Myxoma

open access: yesClinical 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   +4 more
wiley   +1 more source

Clinical characteristics of the primary hepatic malignant fibrous histiocytoma in China: case report and review of the literature

open access: yesWorld Journal of Surgical Oncology, 2012
Background A malignant fibrous histiocytoma is a soft tissue tumor that most commonly occurs in the extremities, but rarely involves the liver. The clinical characteristics and therapeutic experiences of primary hepatic malignant fibrous histiocytoma are
Yao Dianbo, Dai Chaoliu
doaj   +1 more source

Soft tissue sarcomas with complex genomic profiles [PDF]

open access: yes, 2018
Soft tissue sarcomas (STS) with complex genomic profiles (50% of all STS) are predominantly composed of spindle cell/pleomorphic sarcomas, including leiomyosarcoma, myxofibrosarcoma, pleomorphic liposarcoma, pleomorphic rhabdomyosarcoma, malignant ...
Aurias, Alain, Guillou, Louis
core  

Solitary fibrous tumor of the parotid gland: case report [PDF]

open access: yes, 2013
Solitary fibrous tumor (SFT) is a rare spindle cell neoplasm that usually develops in the pleura and peritoneum. The head and neck region is involved in only 6% of the cases.
Gomez, Ricardo Santiago   +5 more
core   +1 more source

Clinical Outcomes and Prognosis in Atypical Fibroxanthoma: A Systematic Review and Meta‐Analysis

open access: yesInternational Journal of Dermatology, Volume 64, Issue 9, Page 1592-1598, September 2025.
ABSTRACT Atypical fibroxanthoma (AFX) is a rare dermal spindle‐cell tumor characterized by a generally benign clinical course. Despite recent advances, there are still challenges regarding its accurate diagnosis, prognostic indicators, and optimal management strategies.
Rebecca von Dannecker   +8 more
wiley   +1 more source

Benign fibrous histiocytoma of larynx: A rare cause of acute airway obstruction

open access: yesLung India, 2010
Fibrous histiocytoma of larynx is a rare entity. We herein present a 35-year-old femaleof benign fibrous histiocytoma of larynx with severe airway obstruction that requiring urgent endotracheal intubation followed by tracheostomy. We also report the good
Gupta Shiv, Singhal Sanjay
doaj  

Pseudoglandular Schwannoma With FUS::KLF17 Fusion: Broadening the Spectrum of FUS‐Associated Tumors

open access: yesGenes, Chromosomes and Cancer, Volume 64, Issue 8, August 2025.
ABSTRACT We present a case of a 51‐year‐old male with a pseudoglandular cellular schwannoma arising from the brachial plexus, which contains the expected molecular aberrations for a schwannoma (chromosome 22q loss encompassing the NF2 and LZTR1 genes) as well as a FUS::KLF17 rearrangement.
Jerome Givi   +4 more
wiley   +1 more source

Case of Monostotic Fibrous Dysplasia in the hand [PDF]

open access: yes, 2002
A case of monostotic fibrous dysplasia in the proximal phalanx of an otherwise healthy, twenty-five year old is discussed. Fibrous dysplasia in the hand is rarely seen. Our patient presented with a swelling in his proximal phalanx.
Attard, Gerhardt   +2 more
core  

Synergistic effects of targeted PI3K signaling inhibition and chemotherapy in liposarcoma. [PDF]

open access: yes, 2014
While liposarcoma is the second most common soft tissue malignant tumor, the molecular pathogenesis in this malignancy is poorly understood. Our goal was therefore to expand the understanding of molecular mechanisms that drive liposarcoma and identify ...
Borger, Darrell R   +12 more
core   +2 more sources

Soft tissue sarcomas at a glance: clinical, histological, and MR imaging features of malignant extremity soft tissue tumors [PDF]

open access: yes, 2009
Soft tissue sarcomas comprise approximately 1% of malignant tumors. There are more than 50 subtypes, but pleomorphic sarcoma, liposarcoma, leiomyosarcoma, synovial sarcoma, and malignant peripheral nerve sheath tumor account for 75%.
Dijke, C.F. (Cornelis) van   +3 more
core   +3 more sources

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