Necrobiotic Xanthogranuloma of the Eyelid
- 1 January 1983
- journal article
- case report
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 101 (1), 60-63
- https://doi.org/10.1001/archopht.1983.01040010062009
Abstract
• Necrobiotic xanthogranuloma with paraproteinemia is characterized by multiple nodules or plaques that involve the periorbital area along with other parts of the body. A dysproteinemia due to an IgG paraprotein is associated with the condition; low serum complement, cryoglobulinemia, leukopenia, and hyperlipemia are also sometimes seen. Multiple myeloma is present in some cases. Two cases of necrobiotic xanthogranuloma with IgG monoclonal gammopathy were seen. Both initially had ocular symptoms and in the second case, the ocular manifestations have dominated the clinical picture. Histologically, these granulomas are characterized by collagen necrobiosis and by the presence of many foamy histiocytes and Touton giant cells. Because necrobiotic xanthogranuloma with monoclonal gammopathy frequently has prominent manifestations in the orbital region, may result in dysfunction of the eyelids or extraocular muscles, and is associated with potentially life-threatening systemic conditions, its recognition by the ophthalmologist is important.Keywords
This publication has 2 references indexed in Scilit:
- Necrobiotic xanthogranuloma with paraproteinemiaJournal of the American Academy of Dermatology, 1980
- Atypical (annular) Necrobiosis Lipoidica of the Face and ScalpDermatology, 1967