Langerhans cell histiocytosis.

Authors

  • Ana Milena Toro
  • Rodrigo Restrepo
  • Amparo Ochoa

Keywords:

Histiocytosis, Langerhans cells, eosinophilic granuloma, skin manifestations

Abstract

Langerhans cell histiocytosis is a clonal anormal proliferation of cells with a positive immunophenotype for S- 100 and CD1a and intracytoplasmic Birbeck granules. It is characterized by variable clinical manifestations from an acute multisystemic disease with high mortality to chronic form with a more bening course.
A review about physiopathology, clinical findings and some important concepts about the diagnosis and treatment is presented.

Author Biographies

Ana Milena Toro

Dermatóloga. Universidad Pontificia Bolivariana. UPB.

Rodrigo Restrepo

Patólogo. Instructor asociado de patología y dermatopatología. UPB

Amparo Ochoa

Dermatóloga y docente de dermatología pediátrica. Universidad de Antioquia.

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How to Cite

1.
Toro AM, Restrepo R, Ochoa A. Langerhans cell histiocytosis. rev. asoc. colomb. dermatol. cir. dematol. [Internet]. 2019 Feb. 12 [cited 2024 Jul. 3];17(1):34-4. Available from: https://revista.asocolderma.org.co/index.php/asocolderma/article/view/148

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Published

2019-02-12

How to Cite

1.
Toro AM, Restrepo R, Ochoa A. Langerhans cell histiocytosis. rev. asoc. colomb. dermatol. cir. dematol. [Internet]. 2019 Feb. 12 [cited 2024 Jul. 3];17(1):34-4. Available from: https://revista.asocolderma.org.co/index.php/asocolderma/article/view/148

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