Degos’ disease: a rare condition simulating rheumatic diseases
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Rheumatology
Link
http://link.springer.com/content/pdf/10.1007/s10067-009-1164-5.pdf
Reference13 articles.
1. Degos R, Delort J, Tricot R (1942) Dermatits papulosquameuse atrophiante. Bull Soc Franc Derm Syph 49:148–150
2. Dubertret L (1993) Malignant atrophic papulosis (Degos’ disease). Dermatology in general medicine. McGraw-Hill, New York
3. Lankish MR, Johst P, Scolapio JS et al (1999) Acute abdominal pain as a leading symptom for Degos disease. Am J Gastroenterol 94:1098–1099
4. Fruhwirth J (1997) Kohlmeier–Degos’ disease with primary intestinal manifestations. Scand J Gastroenterol 32:1066–1070
5. Degos R (1979) Malignant atrophic papulosis. Br J Dermatol 100:21–35
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2. Clinical manifestations and treatment outcomes in degos disease: a systematic review;Journal of the European Academy of Dermatology and Venereology;2021-05-16
3. Benign Atrophic Papulosis (Degos Disease) With Lymphocytic Vasculitis and Lichen Sclerosus-Like Features;The American Journal of Dermatopathology;2018-04
4. Degos disease with an intestinal perforation: a case report;International Journal of Dermatology;2014-02-14
5. Cutaneous Vascular Diseases;Andrews' Diseases of the Skin;2011
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