Erdheim-Chester Disease: Two Cases of Orbital Involvement.
- Author:
Yun Jeong KIM
1
;
Yoon Duck KIM
Author Information
1. Department of Ophthalmology, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul, Korea. ydkim@samsung.co.kr
- Publication Type:Case Report
- Keywords:
Erdheim-Chester disease;
Orbital mass;
Proptosis
- MeSH:
Aged;
Biopsy;
Cardiomyopathy, Dilated;
Diagnosis;
Erdheim-Chester Disease*;
Exophthalmos;
Female;
Giant Cells;
Heart;
Histiocytes;
Humans;
Kidney Failure, Chronic;
Lung;
Lung Diseases;
Middle Aged;
Orbit*;
Osteosclerosis;
Radiography;
Skin;
Steroids;
Tibia
- From:Journal of the Korean Ophthalmological Society
2002;43(7):1323-1329
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: ECD is a rare idiopathic condition characterized by infiltration of the bone, heart, lungs, retroperitoneum, skin, CNS and other tissues by a fibrosing process containing xanthomatous histiocytes and multinucleated giant cells of the Touton type. Orbital involvement of ECD is rare and we report two cases of Erdheim-Chester disease. METHODS: A 46-year-old man with dilated cardiomyopathy and chronic renal failure and a 70-year-old woman with pulmonary disease and intracranial mass visited our clinic because of bilateral proptosis. RESULTS: The systemic evaluation revealed multiple organ involvement, such as bone, heart, lung and retroperitoneum ,while radiography of the tibia showed symmetrical osteosclerosis. The biopsy of tibia revealed a diffuse infiltration of foamy histiocytes and multinucleated giant cells of the Touton type. Based on the diagnosis of ECD, the patients were treated with radiation and steroids. CONCLUSIONS: Although most patients with ECD do not have ocular involvement, the unusual occurrence of bilateral proptosis and diffuse infiltrative orbital masses are suggestive of ECD. These findings should alert the ophthalmologist to this potentially serious systemic disease and prompt an evaluation for systemic manifestations.
