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Hypothalamic hamartoma with neurofibrillary tangles
Yamada, Seiji , Wood, Christopher P. , Shah, Jawad , Vida, Jonathan, Parisi, Joseph E. , Jentoft, Mark E.

Mayo Clinic

Neuropathology | April 19, 2016 | Volume: 36 | Issue: 5 | Pages: 480-484

10.1111/neup.12296 | PMID 27090596 Get It

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.