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Article

Avoid a rash diagnosis: Cytophagic histiocytic panniculitis is a distinct clinical entity

2020-08-27

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Cytophagic histiocytic panniculitis (CHP) is a rare autoimmune disease that can mimic both lupus panniculitis (LP) and subcutaneous panniculitis-like T cell lymphoma (SPTL). Diagnosis is challenging due to overlapping histologic characteristics of these entities. It has historically been considered a pre-malignant lesion, with few case reports detailing CHP as i...

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Literature Corpus work
383af524-367a-56b1-94d5-5cd9b62e2b33
DOI
10.21203/rs.3.rs-64101/v1
Open publication

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Avoid a rash diagnosis: Cytophagic histiocytic panniculitis is a distinct clinical entityDOI 10.21203/rs.3.rs-64101/v1
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