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Year Number of Results
1954 2
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1957 1
1959 1
1961 2
1963 1
1964 2
1965 1
1966 1
1967 2
1968 5
1969 5
1970 1
1971 2
1972 1
1973 3
1974 4
1975 2
1976 5
1977 5
1978 3
1979 4
1980 4
1981 3
1982 3
1983 3
1984 6
1985 1
1986 5
1987 4
1988 4
1989 2
1990 4
1991 2
1992 2
1993 3
1994 2
1995 2
1996 2
1997 4
1998 3
1999 2
2000 1
2001 3
2002 4
2003 5
2004 2
2005 4
2006 3
2007 4
2008 15
2009 15
2010 11
2011 12
2012 4
2013 10
2014 12
2015 10
2016 5
2017 12
2018 8
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2020 13
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2023 11
2024 3

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294 results

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Page 1
Malignant Atrophic Papulosis.
Rice AS, Zedek D. Rice AS, et al. 2023 Aug 7. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Aug 7. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 31335049 Free Books & Documents.
Malignant atrophic papulosis, otherwise known as Kohlmeier-Degos disease or Degos disease, is a rare disorder of thrombo-obliterative vasculopathy affecting the skin, gastrointestinal tract, and central nervous system. ...Subsequently, the disea
Malignant atrophic papulosis, otherwise known as Kohlmeier-Degos disease or Degos disease, is a rare diso
Atrophic Papulosis.
Robert M, Hot A. Robert M, et al. Dermatology. 2023;239(2):177-187. doi: 10.1159/000526789. Epub 2022 Nov 9. Dermatology. 2023. PMID: 36353773 Free article. Review.
Atrophic papulosis (Kohlmeier-Degos disease) in children and adolescents-A cross-sectional study and literature review.
Zouboulis CC, Kaleta KP, Broniatowska E, Jarienė V, Nikolakis G. Zouboulis CC, et al. J Eur Acad Dermatol Venereol. 2023 Apr;37(4):810-816. doi: 10.1111/jdv.18844. Epub 2023 Jan 14. J Eur Acad Dermatol Venereol. 2023. PMID: 36606530 Review.
BACKGROUND: Atrophic papulosis (Kohlmeier-Degos disease, Degos disease) is a rare thrombo-obliterative microangiopathy of unknown pathogenesis. ...
BACKGROUND: Atrophic papulosis (Kohlmeier-Degos disease, Degos disease) is a rare thrombo-obliterative microangiopathy of unkn …
Malignant atrophic papulosis (Kohlmeier-Degos disease) - a review.
Theodoridis A, Makrantonaki E, Zouboulis CC. Theodoridis A, et al. Orphanet J Rare Dis. 2013 Jan 14;8:10. doi: 10.1186/1750-1172-8-10. Orphanet J Rare Dis. 2013. PMID: 23316694 Free PMC article. Review.
DEFINITION OF THE DISEASE: Malignant atrophic papulosis (MAP), described independently by Kohlmeier and Degos et al., is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central porcelain-white atrophy and surround …
DEFINITION OF THE DISEASE: Malignant atrophic papulosis (MAP), described independently by Kohlmeier and Degos et al., i …
Atrophic papulosis (Kohlmeier-Degos disease) revisited: a cross-sectional study on 105 patients.
Kaleta KP, Jarienė V, Theodoridis A, Nikolakis G, Zouboulis CC. Kaleta KP, et al. J Eur Acad Dermatol Venereol. 2022 Nov;36(11):2190-2194. doi: 10.1111/jdv.18260. Epub 2022 Jun 7. J Eur Acad Dermatol Venereol. 2022. PMID: 35610757
The classification into a benign, merely cutaneous disease (benign atrophic papulosis), and malignant atrophic papulosis, associating cutaneous and visceral lesions was confirmed due to their striking prognostic difference. Benign atrophic papulosis was detec …
The classification into a benign, merely cutaneous disease (benign atrophic papulosis), and malignant atrophic papulosis
Malignant atrophic papulosis.
Scheinfeld N. Scheinfeld N. Clin Exp Dermatol. 2007 Sep;32(5):483-7. doi: 10.1111/j.1365-2230.2007.02497.x. Clin Exp Dermatol. 2007. PMID: 17692056 Review.
Malignant atrophic papulosis (MAP; also known as Degos' disease) has a purely cutaneous variant and a systemic variant with cutaneous manifestations. ...
Malignant atrophic papulosis (MAP; also known as Degos' disease) has a purely cutaneous variant and a systemic variant
Malignant Atrophic Papulosis.
Mareschal A, Razanamahery J, Aubin F. Mareschal A, et al. JAMA Dermatol. 2020 Feb 1;156(2):204. doi: 10.1001/jamadermatol.2019.3726. JAMA Dermatol. 2020. PMID: 31799991 No abstract available.
Malignant atrophic papulosis.
Degos R. Degos R. Br J Dermatol. 1979 Jan;100(1):21-35. doi: 10.1111/j.1365-2133.1979.tb03566.x. Br J Dermatol. 1979. PMID: 371654 Review.
The lethal intestino-cutaneous syndrome which we described in 1942 as malignant atrophic papulosis (MAP) has gained various other visceral sites. ...
The lethal intestino-cutaneous syndrome which we described in 1942 as malignant atrophic papulosis (MAP) has gained var …
Malignant and benign forms of atrophic papulosis (Kohlmeier-Degos disease): systemic involvement determines the prognosis.
Theodoridis A, Konstantinidou A, Makrantonaki E, Zouboulis CC. Theodoridis A, et al. Br J Dermatol. 2014 Jan;170(1):110-5. doi: 10.1111/bjd.12642. Br J Dermatol. 2014. PMID: 24116834
BACKGROUND: Atrophic papulosis (Kohlmeier-Degos disease) is a rare disease of unknown aetiology. The cutaneous signs--papular skin lesions with central porcelain-white atrophy and surrounding telangiectatic rim--are almost pathognomonic. ...The cumulative 5-year sur …
BACKGROUND: Atrophic papulosis (Kohlmeier-Degos disease) is a rare disease of unknown aetiology. The cutaneous signs--papular …
Malignant atrophic papulosis (Degos disease).
Xu Q, Lin M, Zhang L, Chen S, Gong T, Cheng B, Ji C. Xu Q, et al. Australas J Dermatol. 2021 Nov;62(4):e586-e588. doi: 10.1111/ajd.13722. Epub 2021 Sep 27. Australas J Dermatol. 2021. PMID: 34570365
Malignant atrophic papulosis (Degos disease) is a rare syndrome of multiple-system vascular diseases with unknown etiology. ...Based on the clinical manifestations, skin biopsy and colonoscopy, a diagnosis of malignant atrophic papulosis
Malignant atrophic papulosis (Degos disease) is a rare syndrome of multiple-system vascular diseases with unknown etiol
294 results