Results 61 to 70 of about 168,404 (247)
Intercalary bone allografts 23 tumor cases followed for 3 years [PDF]
, 1994 From 1987 to 1991, 26 patients with malignant bone tumors (osteosarcoma, Ewing's sarcoma, chondrosarcoma and malignant fibrous histiocytoma) in the diaphysis or metaphysis of long bones have been treated by chemotherapy, radiotherapy and intercalary bone
Cara, J.A. (José Antonio) +2 more
core +1 more source
Storiform-Pleomorphic Type of Multifocal Malignant Fibrous Histiocytoma of the Lumbar Spine
The American journal of case reports, 2014 Patient: Male, 67 Final Diagnosis: Malignant fibrous histiocytoma Symptoms: Back pain • leg weakness • weight loss Medication: — Clinical Procedure: — Specialty: — Objective: Rare disease Background: We present the extremely rare case of a 67-year-old ...
Aykut Akpınar +3 more
semanticscholar +1 more source
Immunity, Inflammation and Disease, Volume 14, Issue 1, January 2026.ABSTRACT Background Chronic expanding hematoma is defined as a progressively enlarging soft tissue mass persisting beyond 1 month, typically resulting from prior trauma or surgical procedures. Although the condition is rare, its occurrence within deep musculature—particularly with bilateral involvement of the gluteus maximus—is exceedingly uncommon. No
Xi‐Qing Pan +6 more
wiley +1 more source
Deep benign fibrous peritoneal histiocytoma in a 14 month-old child. Case report
Iatreia, 2015 Benign fibrous histiocytoma is very rare in children, and more frequent in adults. It is commonly found in the skin, especially in the limbs. Usually it is small.
Herrera-Toro, Natalia +1 more
doaj +1 more source
Istiocitoma fibroso maligno mediastino-polmonare. Aspetti clinici, istiopatologici, terapeutici. Contributo casistico [PDF]
, 1983 no ...
Fontana, G +5 more
core
ALK Expression in Nerve Sheath Myxoma: A Potential Diagnostic Pitfall
Journal of Cutaneous Pathology, EarlyView.
Daniel Cole +6 more
wiley +1 more source
Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.LFS with TP53 disease‐causing mutations may be potential beneficiaries of immune checkpoint inhibitors and targeted therapies. Therefore, NGS and PD‐L1 testing should be performed in all LFS patients. ABSTRACT Background Li‐Fraumeni syndrome is a rare autosomal dominant disorder caused by a pathogenic mutation of the tumor suppressor gene TP53.
Keyu Chen +6 more
wiley +1 more source
Malignant fibrohistiocytoma of the parotid region : report of a case [PDF]
, 2008 Most salivary gland tumors are benign, malignant lesions accounting for 15-30% of the total. The most frequent site of salivary gland neoplasms is the parotid gland (80% of all cases).
Alba García, José Ramón +4 more
core
Commentary on "a case of paratesticular leiomyosarcoma successfully treated with orchiectomy and chemotherapy" [PDF]
, 2015 We have read with great interest the article written by Ko and colleagues on a particularly rare type of malignant mesenchymal tumor that is paratesticular leiomyosarcoma and we did appreciate the argumentation on the utility of adjuvant chemotherapy as ...
Marchetti, Paolo +3 more
core +1 more source
Recurrent aneurysmal fibrous histiocytoma [PDF]
Journal of Clinical Pathology, 2004 Aneurysmal fibrous histiocytoma is a rare variant of cutaneous fibrous histiocytoma that results from blood vessel proliferation and haemorrhage into a fibrous histiocytoma. The resulting lesion has a very different clinical appearance, hence the potential confusion with other skin lesions.
K M, Sheehan +4 more
openaire +2 more sources