2018
DOI: 10.1016/j.jdcr.2018.05.025
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Rare presentation of erythema elevatum diutinum

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Cited by 9 publications
(20 citation statements)
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References 9 publications
(9 reference statements)
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“…EED has been associated with a variety of systemic disorders, including autoimmune, inflammatory, infectious and haematological diseases. EED manifesting as palmoplantar nodules has been reported in association with multiple myeloma, paraproteinaemias, HIV, and hepatitis B and C infections 2 . An annular plaque‐like morphology has been described in association with HIV and IgA gammopathy 3 .…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…EED has been associated with a variety of systemic disorders, including autoimmune, inflammatory, infectious and haematological diseases. EED manifesting as palmoplantar nodules has been reported in association with multiple myeloma, paraproteinaemias, HIV, and hepatitis B and C infections 2 . An annular plaque‐like morphology has been described in association with HIV and IgA gammopathy 3 .…”
Section: Discussionmentioning
confidence: 99%
“…palmoplantar nodules has been reported in association with multiple myeloma, paraproteinaemias, HIV, and hepatitis B and C infections. 2 An annular plaque-like morphology has been described in association with HIV and IgA gammopathy. 3 However, many cases do not have any systemic association.…”
Section: P Dmentioning
confidence: 99%
“…Clinically, it consists of symmetrical erythematous to purple nodules and plaques with a predilection for the extensor surfaces overlying joints, particularly hands, feet, elbows, and knees. To date, palmar involvement has been reported only in a few patients 1–5 . Lesions are mostly asymptomatic, although some patients can experience pruritus, tenderness, and a burning sensation after the onset of new lesions 1 …”
Section: Discussionmentioning
confidence: 99%
“…This fibrosis may display a storiform or concentric appearance, and progression of the lesion is hypothesized to be due to continued foci of leukocytoclastic vasculitis. 3 , 4 Central zone of brightly eosinophilic fibrin surrounded by a palisaded layer of histiocytes and granulation tissue – Incorrect. This histology is characteristic of rheumatoid nodules.…”
Section: Case Reportmentioning
confidence: 99%
“…This fibrosis may display a storiform or concentric appearance, and progression of the lesion is hypothesized to be due to continued foci of leukocytoclastic vasculitis. 3 , 4 …”
Section: Case Reportmentioning
confidence: 99%