We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
A Rare Co-existence of Langerhans Cell Histiocytosis and Lichen Planus.
- Authors
Salunke, Aarti S.; Gosavi, Anil P.; Chavan, Ravindranath B.; Patil, Pallavi Prataprao
- Abstract
Langerhans cell histiocytosis (LCH) is the commonest of the histiocytic disorders. Owing to the relative rarity of the condition, it remains a disease in which the diagnosis is often delayed or missed. Commonly seen in infancy or early childhood, the disorder is characterized by proliferation of abnormal and clonal Langerhans cells in skin, bone, lymph nodes, lungs, liver, spleen, and bone marrow. Lichen planus presents as purple, polygonal, pruritic, papular eruption of unknown etiology affecting skin, mucous membranes and nails. Despite of thourough literature search, we could not find any association of lichen planus with LCH. Hereby, we report a case of five year old child with acute onset of polymorphic eruptions all over the body which on histopathology and Immunohistochemistry showed features of Langerhans cell histiocytosis and lichen planus on bilateral lower limb.
- Subjects
LANGERHANS-cell histiocytosis; LICHEN planus; RARE diseases
- Publication
Indian Journal of Paediatric Dermatology, 2018, Vol 19, Issue 1, p74
- ISSN
2319-7250
- Publication type
Article
- DOI
10.4103/ijpd.IJPD_147_16