Hypothalamic hamartoma with neurofibrillary tangles

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

doi:10.1111/neup.12296

Hypothalamic hamartoma with neurofibrillary tangles

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

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Abstract

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.

Original language	English
Pages (from-to)	480-484
Number of pages	5
Journal	Neuropathology
Volume	36
Issue number	5
DOIs	https://doi.org/10.1111/neup.12296
Publication status	Published - 01-10-2016
Externally published	Yes

All Science Journal Classification (ASJC) codes

Pathology and Forensic Medicine
Clinical Neurology

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10.1111/neup.12296

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title = "Hypothalamic hamartoma with neurofibrillary tangles",

abstract = "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.",

author = "Seiji Yamada and Wood, \{Christopher P.\} and Shah, \{Jawad A.\} and Jonathan Vida and Parisi, \{Joseph E.\} and Jentoft, \{Mark E.\}",

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AU - Yamada, Seiji

AU - Wood, Christopher P.

AU - Shah, Jawad A.

AU - Vida, Jonathan

AU - Parisi, Joseph E.

AU - Jentoft, Mark E.

PY - 2016/10/1

Y1 - 2016/10/1

N2 - 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.

AB - 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.

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EP - 484

JO - Neuropathology

JF - Neuropathology

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Hypothalamic hamartoma with neurofibrillary tangles

Abstract

All Science Journal Classification (ASJC) codes

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