PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Peripheral Nervous System Neoplasms”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 217 records · Page 12Linked to original sources
PubMed2005

Atypical midface tumor complicating nevus of ota.

In the differential diagnosis of midface masses, the nevus of Ota (also called oculodermal melanocytosis) is a rare entity. We present a case of a young white man, who lost his left eye function by progression of a melanocytotic lesion involving the ophthalmic (VI) and maxillary (VII) divisions of the trigeminal nerve. The time course, distribution along the trigeminal nerve, and characteristic MR signal intensities of the lesion, in correlation with the clinical, ophthalmological, and dermatological findings, point to the correct diagnosis.

Adolescent↗
PubMed1991

Vidian metastasis of adenoid cystic carcinoma.

Head and neck tumors may invade perineural space, especially the maxillary division of the trigeminal nerve and the pterygopalatine fossa (PPF). Computed tomography (CT) and magnetic resonance imaging (MRI) signs of perineural extension include essentially the obliteration of the PPF fatty content and the enlargement and erosion of neural foramina. We report a case of perividian metastasis studied with CT and MRI.

Aged↗
PubMedDate not supplied

Imaging features of peripheral neurogenic tumors.

Peripheral nerve sheath tumors (PNST) include schwannoma, neurofibroma and malignant peripheral sheath tumors. All neurogenic tumors share the same imaging characteristics, including fusiform shape, low attenuation on CT, fascicular sign, split fat sign and associated muscle atrophy. The aim of this article is to give a comprehensive overview of peripheral nerve tumors and to discuss the imaging characteristics that distinguish these masses.

Diagnosis, Differential↗
PubMedDate not supplied

Malignant pigmented spinal nerve root schwannoma metastasizing in the brain and viscera.

A 46-year-old woman suffered a meningococcal meningitis followed by a rapidly progressive lumbosacral pluriradicular syndrome. Myelography showed multiple nodules on the lumbar radices. A biopsy showed tissue with numerous Verocay-like bodies, spindle shaped and lymphocytoid cells which was diagnosed as schwannoma. There was a small group of polygonal cells with somewhat irregular and hyperchromatic nuclei. Postoperatively, she developed intracranial hypertension and died. CT scan and MRI revealed multiple occipital lesions consistent with metastases. At autopsy the cauda equina showed multiple nodular lesions with morphology comparable to the biopsy. However, pigment producing cells were also present. There were metastases with distinct morphological features in the brain, myocardium, thyroid gland and pancreas. Some consisted of pigmented, large, pleomorphic cells, others of non-pigmented, spindle-shaped and less pleomorphic cells. In this case, the diagnosis of metastasizing pigmented schwannoma is the most plausible hypothesis.

Brain Neoplasms↗