National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Necrobiotic xanthogranuloma



Other Names:
NXG
Categories:
This disease is grouped under:

Necrobiotic xanthogranuloma (NXG) is a rare, chronic form of non-Langerhans histiocytosis usually found in older adults.[1][2][3] Xanthogranulomas are lesions made of immune cells known as a histiocytes.[4] The term necrobiotic refers to the buildup of broken down collagen fibers that can be seen under a microscope.[1][2] The typical lesion is a yellow, thickened, or raised lesion (plaque) located around the eyes. In most cases the lesions are associated with conditions in which abnormal proteins are found in the blood (monoclonal gammopathies). NXG is also sometimes associated with blood cancers or lymphoproliferative disorders. [1][2][3] As these blood disorders may arise years after the first NXG lesions appear, lifelong follow-up may be recommended.[2] Approximately 50% of people with NXG have problems with their eyes, such as burning or itching, blurred vision, double vision, bulging of the eyeball, drooping of the eyelid, and restricted eye movement. [2] In most cases, other parts of the body, such as the trunk, legs, face, and arms, are also involved. Internal organs may sometimes be affected.[3] Treatment of NXG can be challenging, but is usually necessary to minimize the risk of skin ulcers and scarring. First-line therapy may include drugs used to treat cancer (such as chlorambucil and melphalan). Additional treatment options include corticosteroids, intravenous immunoglobulin, lenalidomide, interferon, radiation therapy, and surgery. In some cases, the symptoms of NXG may return after treatment. If NXG is associated with a blood cancer or a lymphoproliferative disorder, treatment focuses on the blood disorder.[2][3]
Last updated: 11/13/2017

These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

Where to Start

  • DermNet NZ is an online resource about skin diseases developed by the New Zealand Dermatological Society Incorporated. DermNet NZ provides information about this condition.

In-Depth Information

  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Necrobiotic xanthogranuloma. Click on the link to view a sample search on this topic.

Questions sent to GARD may be posted here if the information could be helpful to others. We remove all identifying information when posting a question to protect your privacy. If you do not want your question posted, please let us know.


  1. Cheng, Harriet. Necrobiotic xanthogranuloma pathology. DermNet New Zealand. 2013; https://www.dermnetnz.org/topics/necrobiotic-xanthogranuloma-pathology.
  2. Girisha BS, Holla AP, Fernandes M, Noronha TM. Necrobiotic Xanthogranuloma. Journal of Cutaneous and Aesthetic Surgery. 2012; 5(1):43-45. .https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339130.
  3. Schadt C. and Jacobsen E. Necrobiotic xanthogranuloma. UpToDate. May, 2016; https://www.uptodate.com/contents/necrobiotic-xanthogranuloma.
  4. Achar A, Naskar B, Mondal PC, Pal M. Multiple Generalized Xanthogranuloma In Adult: Case Report And Treatment. Indian Journal of Dermatology. 2011; 56(2):197-99. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108521.