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  2. Ganglioneuroma - Wikipedia

    en.wikipedia.org/wiki/Ganglioneuroma

    A ganglioneuroma is typically asymptomatic, and is typically only discovered when being examined or treated for another condition. Any symptoms will depend upon the tumor's location and the nearby organs affected. [citation needed] For example, a tumor in the chest area may cause breathing difficulty, chest pain, and trachea compression.

  3. Ganglioneuroblastoma - Wikipedia

    en.wikipedia.org/wiki/Ganglioneuroblastoma

    Nodular ganglioneuroblastoma can be divided by prognosis. [2] ... Ganglioneuroma (benign) Ganglioneuroblastoma (intermediate). Neuroblastoma (aggressive) See also.

  4. Ganglioglioma - Wikipedia

    en.wikipedia.org/wiki/Ganglioglioma

    Definitive treatment for ganglioglioma requires gross total surgical resection, and a good prognosis is generally expected when this is achieved. However, indistinct tumor margins and the desire to preserve normal spinal cord tissue, motor and sensory function may preclude complete resection of tumor.

  5. Neuroma - Wikipedia

    en.wikipedia.org/wiki/Neuroma

    Ganglioneuroma - a tumor of the sympathetic nerve fibers arising from neural crest cells. [ 4 ] Pacinian neuroma - a very rare, painful, benign hyperplastic tumor of Pacinian corpuscles ( mechanoreceptors responsible for sensitivity to vibration and pressure ), sometimes linked to a history of local trauma .

  6. Ectomesenchymoma - Wikipedia

    en.wikipedia.org/wiki/Ectomesenchymoma

    Malignant ectomesenchymoma (MEM) is a rare tumor of soft tissues or the CNS, which is composed of both neuroectodermal elements [represented by ganglion cells and/or well-differentiated or poorly differentiated neuroblastic cells such as ganglioneuroma, ganglioneuroblastoma, neuroblastoma, peripheral primitive neuroectodermal tumors – PNET ...

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  8. Paraganglioma - Wikipedia

    en.wikipedia.org/wiki/Paraganglioma

    Most paragangliomas are asymptomatic, present as a painless mass, or create symptoms such as hypertension, tachycardia, headache, and palpitations. [3] While all contain neurosecretory granules, only in 1–3% of cases is secretion of hormones such as catecholamines abundant enough to be clinically significant; in that case manifestations often resemble those of pheochromocytomas (intra ...

  9. 29-Year-Old in ‘Catatonic State’ After Rare Disorder Causes ...

    www.aol.com/lifestyle/29-old-catatonic-state...

    A 29-year-old man’s debilitating night terrors were the first sign of rare autoimmune disorder that rapidly progressed, landing him in the intensive care unit in a “catatonic state.”