Hypothalamic hamartoma with neurofibrillary tangles

Seiji Yamada, Christopher P. Wood, Jawad A. Shah, Jonathan Vida, Joseph E. Parisi, Mark E. Jentoft

研究成果: Article査読

1 被引用数 (Scopus)

抄録

Hypothalamic hamartomas are rare tumors that typically present in childhood, often with gelastic seizures, precocious puberty, or as a manifestation of Pallister‑Hall syndrome. Neurofibrillary tangles are cytoplasmic aggregates of hyperphosphorylated tau that are best recognized in Alzheimer disease, other tau-associated neurodegenerative diseases, or as part of aging, but occasionally may be seen in low-grade neoplasms with a ganglion cell component as gangliocytoma or ganglioglioma. Herein, we report a case of hypothalamic hamartoma with neurofibrillary tangles.

本文言語English
ページ(範囲)480-484
ページ数5
ジャーナルNeuropathology
36
5
DOI
出版ステータスPublished - 01-10-2016
外部発表はい

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Clinical Neurology

フィンガープリント 「Hypothalamic hamartoma with neurofibrillary tangles」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル