Results 31 to 40 of about 95,132 (93)

Factors Contributing to the False Diagnosis of Misleading Dermatofibromas

open access: yesCancer Reports, Volume 8, Issue 2, February 2025.
ABSTRACT Background and Objectives Dermatofibromas (DFs) are common benign skin lesions with unclear etiology, possibly reactive or tumoral. This study aims to evaluate the incidence of DF misdiagnosis and to correlate histopathological findings with clinical interpretations.
Nicholas Florin Kormos   +2 more
wiley   +1 more source

Cervical Angiomatoid Fibrous Histiocytoma [PDF]

open access: yes, 2012
Background: Angiomatoid fibrous histiocytoma (AFH) is a rare type of sarcoma with low-grade malignancy thatusually occurs in young subjects. AFH is uncommon in the head and neck region.Methods: We describe an exceptional case of localization in the neck.
Arnaud, Sebestian; Head and Neck Surgery Department University Hospital of Montpellier Montpellier France   +3 more
core  

Malignant Fibrous Histiocytoma of the Sinonasal Tract.

open access: yes, 2009
BACKGROUND: Sinonasal malignant fibrous histiocytoma (MFH) is rare. METHODS: Twenty-five patients were registered with a diagnosis of sinonasal MFH at our hospital in the past 30 years. Clinical data were retrospectively reviewed.
WANG, CHENG-PING;CHANG, YIH-LEONG;TING, LAI-LEI;YANG, TSUNG-LIN;KO, JENQ-YUH;LOU, PEI-JEN   +1 more
core   +1 more source

Chondroblastoma‐Like Chondroma of Soft Tissue Arising at the Outer Canthus: A Case Report

open access: yesCase Reports in Ophthalmological Medicine, Volume 2025, Issue 1, 2025.
Chondroblastoma‐like chondroma is a rare variant of soft tissue chondroma that can mimic bone‐origin chondroblastoma histologically. Its occurrence in the periocular region is extremely rare. We report a 31‐year‐old woman with a painless, slowly enlarging nodule at the right outer canthus.
Dejan M. Rašić   +3 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.
Sciberras, Carmel   +2 more
core  

Atypical Cutaneous Fibrous Histiocytoma: An Unusual and Misleading Variant of Fibrous Histiocytoma [PDF]

open access: yes, 2011
Atypical fibrous histiocytoma is a distinctive variant of cutaneous fibrous histiocytoma, which is often mistaken histologically for sarcoma and which have a tendency to recur locally and a capacity to metastasize, although very rarely.
Moncef Mokni   +7 more
core   +1 more source

Comprehensive clinicopathological, molecular, and methylation analysis of mesenchymal tumors with NTRK and other kinase gene aberrations

open access: yesThe Journal of Pathology, Volume 263, Issue 1, Page 61-73, May 2024.
Abstract Alterations in kinase genes such as NTRK1/2/3, RET, and BRAF underlie infantile fibrosarcoma (IFS), the emerging entity ‘NTRK‐rearranged spindle cell neoplasms’ included in the latest WHO classification, and a growing set of tumors with overlapping clinical and pathological features.
Natálie Klubíčková   +26 more
wiley   +1 more source

Angiomatoid Fibrous Histiocytoma [PDF]

open access: yes, 2014
Anjiomatoid fibröz histiositom nadir görülen bir yumuşak doku tümörüdür. Düşük grade malign potansiyele sahiptir. En sık görülme yerleri alt ve üst ekstremitelerdir. Ekstremiteleri gövde, boyun ve nazolabial bölge takip eder.
Reşorlu, Mustafa   +5 more
core   +1 more source

Aneurysmal Benign Fibrous Histiocytoma with Atrophic Features [PDF]

open access: yes, 2009
Aneurysmal benign fibrous histiocytoma is an uncommon pathologic variant of dermatofibroma. In addition to the features of atypical dermatofibroma, it has large cleft-like or cavernous blood-filled spaces with numerous hemosiderin pigments.
Cho, Soyun   +6 more
core  

Prolonged generalized osteomalacia associated with a sinonasal cavity phosphaturic mesenchymal tumor: A case report

open access: yesClinical Case Reports, Volume 12, Issue 2, February 2024.
Key Clinical Message Phosphaturic mesenchymal tumor (PMT) is a rare disorder primarily affecting the extremities. It is notable for its correlation with hypophosphatemic osteomalacia and high FGF23 serum levels, which results in renal phosphate wasting and clinical symptoms associated with low serum phosphorus.
Mehdi Montazer   +5 more
wiley   +1 more source

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