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Diffuse xanthogranulomatous dermatitis and systemic Langerhans cell histiocytosis: A novel case that demonstrates bridging between non-Langerhans cell histiocytosis and Langerhans cell histiocytosis.

Abstract：

:The advent of electron microscopy and immunohistochemical stains allowed for reclassification of the histiocytoses based on the predominant cell in the infiltrate. Although the current schema simplicity provides a good foundation, some patients display overlapping clinical and immunohistochemical features that defy classification. The patient herein illustrates bridging between histiocytic disorders. Through this case we review the various conditions classified under the non-Langerhans cell histiocytosis and Langerhans cell histiocytosis rubric.

journal_name

J Am Acad Dermatol

journal_title

Journal of the American Academy of Dermatology

authors

Satter EK,Gendernalik SB,Galeckas KJ

doi

10.1016/j.jaad.2008.10.001

subject

Has Abstract

pub_date

2009-05-01 00:00:00

pages

841-8

issue

5

eissn

0190-9622

issn

1097-6787

pii

S0190-9622(08)01226-7

journal_volume

60

pub_type

杂志文章

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