Literature DB >> 19851674

[Langerhans cell histiocytosis: Letterer-Siwe disease - the importance of dermatological diagnosis in two cases].

Leonardo Mello Ferreira1, Paulo Sergio Emerich, Lucia Martins Diniz, Luciene Lage, Isabella Redighieri.   

Abstract

Langerhans cell histiocytosis is defined as a clonal proliferation of Langerhans phenotypic-like cells. Letterer-Siwe disease is the most common and serious of these entities, affecting mainly infants up to two years of age. We present two cases of this rare disease, diagnosed after dermatological examination, highlighting its typical aspects.

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Year:  2009        PMID: 19851674     DOI: 10.1590/s0365-05962009000400013

Source DB:  PubMed          Journal:  An Bras Dermatol        ISSN: 0365-0596            Impact factor:   1.896


  4 in total

1.  Langerhans' cell histiocytosis with neurological injuries diagnosed from a single cutaneous lesion.

Authors:  Andréa Bauer Bannach; Maria Teresa Fernandes Castilho Garcia; Deusita Fernandes Gandia Soares; Antônio Luiz de Arruda Mattos; Tomás Zecchini Barrese; Marilda Aparecida Milanez Morgado de Abreu
Journal:  An Bras Dermatol       Date:  2017 Jul-Aug       Impact factor: 1.896

2.  Severe Langerhans cell histiocytosis in an infant: haemophagocytic syndrome association.

Authors:  Marta Isabel Póvoas; Pedro Pereira Luís; Isabel Esteves; Anabela Ferrão
Journal:  BMJ Case Rep       Date:  2014-10-21

3.  Congenital self-healing reticulohistiocytosis: An atypical presentation acquired in a 10-month-old.

Authors:  Christopher S Yuki; Patrick J Young; Steven Ohsie; Xuan Nguyen
Journal:  Clin Case Rep       Date:  2022-08-18

4.  Cytological diagnosis of Langerhans cell histiocytosis with cutaneous involvement.

Authors:  Sushama A Chandekar; Vinaya B Shah; Vikas Kavishwar
Journal:  J Cytol       Date:  2013-01       Impact factor: 1.000

  4 in total

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