Neuroendocrine cancer blurred vision
Chordomas are slow growing neoplasms arising from notochordal remnants of the axial skeleton.
The second most common site for chordomas, after the sacrococcygeal region, is the base of the skull. Neuroendocrine cancer blurred vision base chordomas commonly result in cranial nerve deficits, such as blurred vision, facial weakness and swallowing difficulty.
Occasionally, chordomas localized in the hypothalamic or pituitary region may lead to pituitary stalk disjunction, pituitary insufficiency and diabetes insipidus.
Studies show selectați semnele specifice viermilor early diagnosis, combined with aggressive surgical resection, offers the best chance for long-term survival. Although optimal treatment consists of wide excision with adjuvant radiotherapy, skull base chordomas are rarely amenable to complete surgical removal.
Traditionally, postoperative irradiation is delivered to doses of cGy; however this approach controls the chordoma only for a neuroendocrine cancer blurred vision years. Prognosis depends on the histological grade of neuroendocrine cancer blurred vision tumor, atypical chordomas showing the lowest survival rate.
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