Results 71 to 80 of about 6,761,428 (165)

Nasal spindle cell tumor with rhabdomyoblastic features: A rare and diagnostically difficult case

SAGE Open Medical Case Reports, 2020
Nasal spindle cell rhabdomyosarcoma is very rare. The tumor is sometimes confused with other spindle cell tumors. We herein report a case of nasal spindle cell tumor in a 62-year-old woman. The patient first presented herself to a medical doctor’s office
Kenichi Mizutani, Motona Kumagai, Akane Aikawa, Shintaro Terahata, Shin Ishizawa, Hiroshi Minato, Takayuki Nojima, Sohsuke Yamada   +7 more
doaj   +1 more source

Clinical features and ultrasound findings of a rare musculoskeletal system disease–neuromuscular choristoma

BMC Musculoskeletal Disorders, 2022
Background Neuromuscular choristomas (NMCs), are extremely rare developmental lesions that, have been previously established associated with recurrent fibromatosis after surgery, leading to several operations or even amputation.
Wen Guo, Hong Wang, Tao Chen, Wei Yang, Shu-Feng Wang, Shan-Lin Chen   +5 more
doaj   +1 more source

Cytologic and Histologic Findings of Extrapleural Solitary Fibrous Tumor: Report of Two Cases

Diagnostic Cytopathology, Volume 54, Issue 2, Page E46-E53, February 2026.
ABSTRACT Solitary fibrous tumors (SFT) are a rare neoplasm of mesenchymal origin. SFT was previously described primarily in the pleura and meninges; however, extrapleural and extra‐meningeal SFT have been reported in almost every anatomic site and account for up to 40% of cases.
Michael Tyler, Katsiaryna Khatskevich, Chadi Hajar, Jack Yang, Hao Liu   +4 more
wiley   +1 more source

Metachronous multifocal desmoid-type fibromatoses along the neuraxis with adenomatous polyposis syndrome

, 2010
Desmoid-type fibromatosis, aggressive fibromatosis, or desmoid tumor is an uncommon benign but locally aggressive fibroblastic lesion. Although intraabdominal desmoid-type fibromatoses are well described in association with adenomatous polyposis syndrome,
Brian K. Owler, K. H. Carlos Chung, Amanda Charlton, Raymond Chaseling, Susan Arbuckle   +4 more
core   +1 more source

APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis [PDF]

, 2018
Familial adenomatous polyposis (FAP) is usually caused by germline mutations in the adenomatous polyposis coli (APC) gene. The classic form is characterized by hundreds to thousands of adenomas in the colorectum and early onset colorectal cancer (CRC) if
Eli Marie Grindedal, Hølmebakk, Toto, Toto Hølmebakk, Norum, Ole-Jacob Anderssen, Åberg, Kristin, Astrid Tenden Stormorken, Stormorken, Astrid T., Kristin Aaberg, Berg, Thomas, Grindedal, Eli Marie, Steigen, Sonja Eriksson, Ole-Jacob Norum, Thomas Berg, Sonja E. Steigen   +13 more
core   +1 more source

Screening-detected desmoid tumor of the breast: findings at conventional imaging and digital breast tomosynthesis

Acta Radiologica Open, 2018
Desmoid tumor of the breast is a rare benign entity that usually is mistaken for carcinoma clinically and radiologically. We report two cases of desmoid tumor of the breast detected by mammography screening using digital breast tomosynthesis (DBT).
Tatjana Samardzic, Jon Lømo, Per Skaane
doaj   +1 more source

Small Nucleotide Variant Analysis Using RNA Fusion Panel (SMURF): Making the Most of RNAseq Data in Solid Tumours

Journal of Clinical Laboratory Analysis, Volume 40, Issue 4, February 2026.
RNA‐based fusion panels using targeted next‐generation sequencing of formalin‐fixed paraffin‐embedded (FFPE) tumour tissue specimens have been used for a few years from patients with various tumour types to detect rearrangements/fusions. Using the bioinformatic approaches the data obtained from RNA sequencing (RNAseq) can also be used for small ...
Pranav Dorwal, Julie Robin, Broden Krause, Patricia Pyrchla, Bin Yuan, Robert Quach, Anna Fong Na Goh, Pamela Htain, Noel Djitro, Amit Kumar, Liyan Song, Priscillia Siswara, Suzanne Svobodova, Peter Kaub, Beena Kumar   +14 more
wiley   +1 more source

Local recurrence after surgery for primary extra-abdominal desmoid-type fibromatosis

, 2013
Background: Desmoid-type fibromatosis is a locally aggressive soft tissue tumour with a biological behaviour that varies between relatively indolent and progressive growth.
Elias, S. G., Van Broekhoven, D. L.M., Van Gorp, J. M.H.H., Van Geel, B. A.N., Wijrdeman, H. K., Verhoef, C., Van Dalen, T., Witkamp, A. J.   +7 more
core   +1 more source

A Case of Rare Desmoid-Type Fibromatosis Presented as a Breast Lump [PDF]

, 2021
Desmoid-type fibromatosis (DF) is a benign but rare soft tissue tumour, occurring only in 2-4 persons in one million of the population . Its local invasiveness and high tendency to recur following resection contribute to its notorious reputation for ...
W Mustapha, Wan Irfan, Wahab, Nur Shahida, Haroon, Raihanah, Hassan, Radhiana   +3 more
core  

Children and Adolescents With Localised Non‐Rhabdomyosarcoma Soft Tissue Sarcoma: Results of the CWS‐96 and CWS‐2002P Prospective Trials With Reclassification of the Trial Data Incorporating the Recent Soft Tissue Sarcoma Registry

Pediatric Blood &Cancer, Volume 73, Issue 2, February 2026.
ABSTRACT Background Here we report the results of the first comprehensive European trials for all soft tissue sarcoma entities, which aimed to develop a new risk stratification system, limit radiotherapy and chemotherapy for low‐/standard‐risk patients, and evaluate different chemotherapy regimens for high‐risk patients.
Amadeus T. Heinz, Anton Schönstein, Ewa Koscielniak, Martin Ebinger, Jörg Fuchs, Semi Harrabi, Christian Vokuhl, Roland Imle, Sabine Stegmaier, Ines B. Brecht, Gustaf Ljungman, Hanna Juntti, Ruth Ladenstein, Bernarda Kazanowska, Thomas Klingebiel, Kristian W. Pajtler, Monika Sparber‐Sauer   +16 more
wiley   +1 more source