Results 91 to 100 of about 20,018 (209)
Gouty tophi presenting as multiple large periarticular masses could be mistaken for rheumatoid nodules, neoplasm, neurofibroma, or infection. Aspiration of synovial fluid from inflamed joints or examination of whitish material expressed though breaks in ...
Michael L. Brit +2 more
core +1 more source
Hypertrophic scars after therapy with CO2 laser for treatment of multiple cutaneous neurofibromas [PDF]
BACKGROUND. CO2 laser surgery is a treatment modality for cutaneous neurofibromas. OBJECTIVE. Hypertrophic and atrophic scars can result from treatment with CO2 laser surgery.
Neumann, H.A.M. (Martino) +2 more
core +3 more sources
Endobronchial neurofibroma [PDF]
N, Srivali, J M, Boland, J H, Ryu
openaire +2 more sources
Solitary eyelid neurofibroma presenting as tarsal cyst: Report of a case and review of literature
Purpose: To report a rare case of solitary eyelid neurofiboma presenting as tarsal cyst. Observation: A 64 year old male, presented with a painless, non progressive swelling in the right upper eye lid.
Nisar Sonam Poonam +3 more
doaj +1 more source
Neurofibroma é uma proliferação hamartomatosa de origem neuromesenquimal. Pode ser encontrado associado à neurofibromatose ou como tumor solitário, sendo sua apresentação subungueal solitária bastante rara.
Dionne de Almeida Stolarczuk +4 more
doaj +1 more source
Kamath, Sriganesh +3 more
openaire +2 more sources
Neurogenic tumors of the liver are very rare, irrespective of associated neurofibromatosis. We report here a well-documented case of benign schwannoma in a 56-year-old woman without neurofibromatosis, including imaging and pathological examinations ...
MORI, KEIICHIRO +4 more
core
Gorlin syndrome in a patient with skin type VI [PDF]
Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare autosomal dominant disorder that is characterized by multiple basal cell carcinomas developing at a young age, keratocystic odontogenic tumors of the jaw, palmar or plantar ...
Anderson, Kathryn L +3 more
core
Background: Neurofibroma type I (NF1) often presents with multiple clinical phenotypes due to mutations of NF1 gene. The aim of this study was to determine the phenotypic and therapeutic relevance of tumor microenvironment in NF1 patients. Methods: Tumor
Jingcun Shi +9 more
doaj +1 more source

