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Xanthelasma and arginine vasopressin deficiency (central diabetes insipidus), think Erdheim Chester disease.
BMJ Case Rep
October 2024
Department of Medicine, Ottawa Hospital, Ottawa, Ontario, Canada
Genetic Aspects of Necrobiotic Xanthogranuloma.
JAMA Dermatol
October 2024
Department of Dermatology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
A Systematic Review of Clinical Features and Treatment Outcomes of Xanthoma Disseminatum.
J Cutan Med Surg
November 2024
Toronto Dermatology Centre, North York, ON, Canada.
Article Synopsis
- Xanthoma disseminatum (XD) is a rare skin condition within the group of non-Langerhans histiocytosis, presenting mainly as yellow-to-brown lesions on the face, flexures, trunk, and genital areas, and often associated with systemic issues.
- A comprehensive review of 151 studies revealed a total of 166 cases, predominantly in females with an average diagnosis age of 35.3 years, indicating the condition's extensive extracutaneous manifestations, including those affecting the pituitary gland and oropharynx.
- Despite various treatment options explored, including cladribine, systemic steroids, and others, there are low complete response rates, highlighting the need for further research to improve management strategies for
Eruptive xanthomas.
N Z Med J
August 2024
Professor, Department of Dermatology, St John's Medical College, Sarjapura Road, Bangalore 560034.
Diffuse planar xanthomatosis in the setting of monoclonal gammopathy of undetermined significance.
J Dermatol
October 2024
Department of Dermatology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
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