"Dermatitis, Exfoliative" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The widespread involvement of the skin by a scaly, erythematous dermatitis occurring either as a secondary or reactive process to an underlying cutaneous disorder (e.g., atopic dermatitis, psoriasis, etc.), or as a primary or idiopathic disease. It is often associated with the loss of hair and nails, hyperkeratosis of the palms and soles, and pruritus. (From Dorland, 27th ed)
Descriptor ID |
D003873
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MeSH Number(s) |
C17.800.174.318 C17.800.815.318
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Concept/Terms |
Dermatitis, Exfoliative- Dermatitis, Exfoliative
- Dermatitides, Exfoliative
- Exfoliative Dermatitides
- Exfoliative Dermatitis
- Dermatitis Exfoliativa
- Erythroderma
- Erythrodermas
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Below are MeSH descriptors whose meaning is more general than "Dermatitis, Exfoliative".
Below are MeSH descriptors whose meaning is more specific than "Dermatitis, Exfoliative".
This graph shows the total number of publications written about "Dermatitis, Exfoliative" by people in this website by year, and whether "Dermatitis, Exfoliative" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2010 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Dermatitis, Exfoliative" by people in Profiles.
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Mohamad J, Nanda A, Pavlovsky M, Peled A, Malchin N, Malovitski K, Pramanik R, Weissglas-Volkov D, Shomron N, McGrath J, Sprecher E, Sarig O. Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis. Exp Dermatol. 2020 08; 29(8):742-748.
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Wolf R, Parish LC, Parish JL. Commentary: The rash from nuisance to life-threatening. Clin Dermatol. 2019 Mar - Apr; 37(2):85-87.
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Krunic AL, Stone KL, Simpson MA, McGrath JA. Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A. Pediatr Dermatol. 2013 Sep-Oct; 30(5):e87-8.
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Pavlovic S, Krunic AL, Bulj TK, Medenica MM, Fong K, Arita K, McGrath JA. Acral peeling skin syndrome: a clinically and genetically heterogeneous disorder. Pediatr Dermatol. 2012 May-Jun; 29(3):258-63.
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Trufant JW, Christensen SR, McNiff JM, Choi JN. Erythroderma and spontaneous blistering in a 49-year-old man. Arch Dermatol. 2010 Dec; 146(12):1419-24.