Results 1 to 10 of about 1,141 (148)
An 8‐year‐old Miniature Poodle presented with chronic sneezing and unilateral epistaxis. A left‐sided intranasal mass was identified on computed tomography.
Dohee Lee +11 more
doaj +2 more sources
Primary Intraosseous Malignant Nerve Sheath Tumor Of Humerus Presenting With Pathological Fracture: A Rare Case Report With Review Of Literature [PDF]
Introduction: Malignant peripheral nerve sheath tumors (MPNST) are rare, aggressive soft-tissue sarcomas arising from peripheral nerves, usually associated with neurofibromatosis Type-I.
Divesh Jalan +5 more
doaj +2 more sources
Gastrointestinal Stromal Tumor Associated with Neurofibromatosis Type 1 Simulating a Neurofibrosarcoma in a Black African Adult Patient [PDF]
Gastrointestinal stromal tumor (GIST) is the most prevalent mesenchymal tumor encountered in patients with neurofibromatosis type I (NF1). This association is rarely reported in black African adult patients.
Gnangoran Marcellin Koffi +3 more
doaj +2 more sources
Clinical Outcomes of Surgical Management of Primary Brachial Plexus Tumors [PDF]
Introduction This study evaluates the clinical presentation, tumor characteristics, and clinical outcomes of surgically treated benign and malignant brachial plexus tumors (BPTs).
Sunil Gaba +4 more
doaj +2 more sources
Neurofibrosarcoma of the mandible derived from neurofibromatosis [PDF]
Neurofibrosarcoma is a rare malignant neoplasm of the head and neck region and accounts for 8% to 16% of all cases. Its origin is varied and may stem from cells of the peripheral nerves, develop de novo, or result from malignant transformation of ...
Juliane Pirágine Araujo +3 more
doaj +2 more sources
Neurofibrosarcoma of lacrimal gland
A rare case of neurofibroma of lacrimal gland showing malignant transformation in a male patient eye 31 years is reported. There was no evidence of recurrence ′on a follow up study.
Pattanayak S +3 more
doaj +2 more sources
Case histories of 10 patients with neurofibrosarcoma, including 14 (70%) with neurofibromatosis, evaluated over 10 years were reviewed to determine the incidence of local and systemic recurrence and the most effective means of therapy for this rare neoplasm. Initial therapy resulted in complete local disease control in only 11 (55%) patients.
F K, Storm +3 more
openaire +3 more sources
Neurofibrosarcoma and the Sign of Leser-Trelat [PDF]
S R, Smalley, J, Rubin, K M, Leiferman
exaly +3 more sources
Peripheral Neural Sheath Breast Sarcoma: Case Report and Literature Review
Primary sarcomas of the breast are heterogeneous neoplasms derived from the non-epithelial elements of the mammary gland. Malignant peripheral nerve sheath tumors comprise 5–10% of all malignant soft tissue sarcomas.
Yency Johana Forero +4 more
doaj +1 more source

