Article Text

Download PDFPDF
Answers to Dermatophile
  1. Vânia Oliveira Carvalho,
  2. Renata Robl,
  3. Marjorie Uber,
  4. Kerstin Taniguchi Abagge,
  5. Leide Parolin Marinoni,
  6. Juliana Gomes Loyola Presa
  1. Division of Pediatric Dermatology, Department of Pediatrics, Federal University of Paraná, Hospital de Clínicas da UFPR, Curitiba, Paraná, Brazil
  1. Correspondence to Vânia Oliveira Carvalho, Department of Pediatric Dermatology, Hospital de Clinicas – UFPR, Rua Richard Strauss 62—Vista Alegre, Curitiba/Paraná; CEP 80-820-110, Brazil; rcarvalho50{at}hotmail.com

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Answers

From the questions on page 185.

Answer to question 1

B—Langerhans cell histiocytosis (LCH): Abnormal clonal proliferation of histiocytes, resembling Langerhans cells, and its accumulation in different tissues and organs. LCH exhibits heterogeneous clinical pictures and evolution—it varies from the isolated cutaneous lesion with spontaneous resolution to severe cases involving the liver, spleen, lung and haematopoietic system.1 The most common skin lesion is similar to seborrhoeic dermatitis, but exhibits petechiae and purpura, and affects the scalp, eyebrows, ears and intertriginous areas.2 Seborrhoeic-like plaques resistant to conventional therapy, no improvement until 8 months of age (both facts described in case number 1), as well as the presence of hepatosplenomegaly should indicate the hypothesis of LCH and, therefore, skin biopsy …

View Full Text

Footnotes

  • Competing interests None.

  • Patient consent Obtained.

  • Ethics approval Comite de Ética do Hospital de Clinicas da UFPR.

  • Provenance and peer review Not commissioned; internally peer reviewed.