Literature DB >> 26990538

Langerhans cell histiocytosis mimicking lichen nitidus with bone involvement.

Belén Lozano Masdemont1, Laura Gómez-Recuero Muñoz1, Ana Villanueva Álvarez-Santullano1, Verónica Parra Blanco2, Minia Campos Domínguez1.   

Abstract

We report the case of a 6-month-old Hispanic boy with a 4-month history of widespread pruritic hypopigmented papules mimicking lichen nitidus. The final diagnosis was multisystem non-risk-organ Langerhans cell histiocytosis (LCH), with cutaneous and multiple bone involvement. With this patient and others previously reported in the literature, we suggest an early biopsy of the hypopigmented rash in children.
© 2016 The Australasian College of Dermatologists.

Entities:  

Keywords:  Langerhans cell histiocytosis; bone involvement; hypopigmentation; lichen nitidus

Mesh:

Year:  2016        PMID: 26990538     DOI: 10.1111/ajd.12467

Source DB:  PubMed          Journal:  Australas J Dermatol        ISSN: 0004-8380            Impact factor:   2.875


  2 in total

1.  Langerhans cell histiocytosis in an adult female with atypical swellings.

Authors:  Prakriti Shukla; Parul Verma; Rashmi Kushwaha; Shailendra Verma; Geeta Yadav; Aftab Hasan Nazar
Journal:  Indian J Dermatol Venereol Leprol       Date:  2021 Mar-Apr       Impact factor: 2.545

Review 2.  Childhood Langerhans cell histiocytosis: a disease with many faces.

Authors:  Alexander K C Leung; Joseph M Lam; Kin Fon Leong
Journal:  World J Pediatr       Date:  2019-08-28       Impact factor: 2.764

  2 in total

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