Korean J Dermatol.
2000 Feb;38(2):191-197.
Langerhans Cell Histiocytosis in Children: Report of six cases with
clinicopathological observation
- Affiliations
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- 1Department of Dermatology, Yonsei University College of Medicine, Seoul, Korea.
- 2Department of Pathology, Yonsei University College of Medicine, Seoul, Korea.
Abstract
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BACKGROUND: Langerhans cell histiocytosis (LCH) is a broad spectrum of clinical diseases
having proliferation of Langerhans cells in common. LCH may be manifested in a variety of
ways, ranging from a spontaneously regressing skin lesion to a multisystemic life-threatening
disorder. Congenital self-healing reticulohistiocytosis is widely regarded as a limited form
of LCH. It is present at birth or shortly thereafter and involute spontaneously.
OBJECTIVE
Our purpose was to investigate the relationship between clinicopathologic
characteristics and prognosis of LCH in children.
METHODS
Six children with LCH were investigated clinically and histopathologically.
Immunostains were performed with CD1a and S100 antibodies in 5 cases using paraffin-embedded
sections and an electron microscopic examination was done in 1 case.
RESULTS
Among the 6 cases of LCH, 4 cases were confined to the skin, and 2 cases showed
internal organ involvement. All LCH confined to the skin showed resolution of the skin lesion
in 1 year, and 2 cases involving internal organ showed bad prognosis.
Histopathological findings showed large histiocytes with eosinophilic cytoplasm in common.
Immunohistochemical stains (5 cases) showed positive reactions with CD1a and S-100, and
electron- microscopical observation in one case demonstrated laminated dense bodies. There
was no significant histopathological or immunohistochemical difference between LCH confined
to the skin which showed resolution of lesions and LCH involving internal organs with grave
prognosis.
CONCLUSIONS
Clinical types of Langerhans cell histiocytosis could not be differentiated
only from the histopathological findings of the skin. The distinction between Langerhans
cell histiocytosis confined to the skin showing spontaneous resolution and congenital
self-healing reticulohistiocytosis remains to be clarified.