Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Photophobia

Excessive sensitivity to light with the sensation of discomfort or pain in the eyes due to exposure to bright light.

合計: 1

（表示件数）

PMID (PMCID)
21168078	MALE	Child
	Langerhans cell histiocytosis of the uvea with neovascular glaucoma: diagnosis by fine-needle aspiration biopsy and management with intraocular bevacizumab and brachytherapy.
	Shields CL, Hogarty MD, Kligman BE, Christian C, Ehya H, Shields JA. J AAPOS. 2010;14(6):534-7.
	A 6-year-old boy with known multisystem Langerhans cell histiocytosis developed photophobia, conjunctival injection, iris neovascularization, and an iridociliochoroidal mass.