Homonymous hemianopia due to Erdheim-Chester disease.

Autor: Hills WL; Department of Neuro-Ophthalmology (WLH, JF), Casey Eye Institute, Oregon Health & Science University, Portland, Oregon; Departments of Neurology (WLH) and Ophthalmology (WLH, JF), Oregon Health & Science University, Portland, Oregon; Arab Organization for Industrialization Hospital (AN), Cairo, Egypt; Department of Neuropathology (MRG), Oregon Health & Science University, Portland, Oregon; University of Pennsylvania School of Medicine (SJM), Philadelphia, Pennsylvania; Department of Radiology, Ophthalmology, and Otolaryngology (JLW), Oregon Health & Science University, Portland, Oregon; Department of Pathology (SKM, MTC), Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania; Department of Neuro-Ophthalmology (MLM), Wills Eye Institute, Philadelphia, Pennsylvania; and Departments of Neurology (MLM) and Ophthalmology (MLM), Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania., Nassef AH, Grafe MR, Weissman JL, Moster SJ, Falardeau J, Mardekian SK, Curtis MT, Moster ML
Jazyk: angličtina
Zdroj: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society [J Neuroophthalmol] 2014 Sep; Vol. 34 (3), pp. 237-42.
DOI: 10.1097/WNO.0000000000000111
Abstrakt: Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis typically affecting multiple organ systems. We report 2 patients who presented with homonymous hemianopia and were ultimately diagnosed with biopsy-confirmed ECD. We review the spectrum of ECD and its treatment as well as histopathological and immunohistochemical differentiation from other histiocytic disorders.
Databáze: MEDLINE