Results 91 to 100 of about 29,620 (204)
Plexiform Neurofibroma of the Submandibular Salivary Gland in a Child
Plexiform neurofibromas in major salivary glands are rarely described. In the literature, most reported tumours have been present in the parotid gland region.
Jacqueline M Bourgeois +3 more
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Plexiform neurofibromas are benign tumors originating from subcutaneous or visceral peripheral nerves, which are usually associated with neurofibromatosis type 1.
Roberto Vélez +5 more
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Morphological spectrum of peripheral nerve sheath tumors: A series of 126 cases
By convention, soft tissue tumors include the peripheral nerve sheath tumor (PNST) although they arise from neuroectoderm. PNSTs display a wide spectrum of morphology and biological behavior.
Gabhane Sushma +2 more
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Pelvic neurofibroma arising from prostate in a case of neurofibromatosis-1
Pelvic neurofibroma is a rare condition and can be associated with neurofibromatosis-1 (NF-1). The diagnosis is primarily based on histopathology, though certain characteristic imaging features like the ′target sign′ on T2W MRI are highly suggestive of ...
Manisha Jana +3 more
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Neurofibromatosis type I (NF1) is an autosomal dominant genetic condition characterized by peripheral nervous system tumors (PNSTs), including plexiform neurofibromas (pNFs) that cause nerve dysfunction, deformity, pain damage to adjacent structures, and
M. Ferrer +15 more
semanticscholar +1 more source
A case of large diffuse cutaneous neurofibroma masquerading as plexiform variant: Diagnostic challenges [PDF]
Diffuse Cutaneous Neurofibroma (DCN) is an infrequently encountered clinical entity that can be challenging to diagnose due to its variable clinical presentation, radiological findings, and histopathological features.
Shivani S Rao , Ranjana S Ranade
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Plexiform neurofibroma in the hepatic hilum associated with neurofibromatosis type 1: case report
We present an extremely rare case of plexiform neurofibroma involving the hepatic hilum. A 24-year old woman who had been diagnosed with neurofibromatosis type 1 was referred to our hospital for evaluation of an abdominal mass found on computed ...
Sojun Hoshimoto +8 more
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Neurofibromatosis type (NF1) is an autosomal dominant inherited tumor-suppressor gene syndrome of significant phenotypic variability with probable complete penetrance of the disease. Skeletal malformations of the skull belong to the phenotype of NF1.
R. Friedrich, H. Scheuer
semanticscholar +1 more source
Secondary Hip Osteoarthritis due to Neurofibroma Treated with Total Hip Replacement
Background. Local plexiform neurofibroma can lead to deformity of the pelvis, valgus deformity of femoral neck, and joint capsule laxity. We report a case of secondary hip osteoarthritis with subluxation and coxa vara deformity resulting from an extra ...
Suksan Tangsataporn +5 more
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Facial plexiform neurofibroma in a 13-year-old girl with neurofibromatosis-1
Neurofbromatosis (NF) is an autosomal dominant disorder that affects the bone, the nervous system, soft tissue and the skin. NF is a neurocutaneous condition that can involve almost any organ system existing in two subtypes.
Satya Ranjan Misra +3 more
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