Korean J Dermatol.  2000 Dec;38(12):1688-1690.

A Case of Letterer-Siwe Disease in Adult

Affiliations
  • 1Department of Dermatology, Inha University College of Medicine, Inchon, Korea.

Abstract

Letterer-Siwe disease is a one of Langerhans cell histiocytosis and characterized by proliferation of Langerhans cells. It's clinical features are onset of infancy, hemorrhagic crusted papules and petechiae, hepatomegaly, lymphadenopathy, localized bone defect, and fatal outcome. We report a 38-year-old woman with hepatomegaly, lymphadenopathy, scaly papules and petechiae on the trunk. The eletronmicroscopy showed a tennis racquet shaped Birbeck granules in cytoplasm of histiocyte. Systemic treatment with etoposide, cyclophosphamide, prednisone, and vincristine was effective.

Keyword

Letterer-Siwe disease; Langerhans cells; Adult

MeSH Terms

Adult*
Cyclophosphamide
Cytoplasm
Etoposide
Fatal Outcome
Female
Hepatomegaly
Histiocytes
Histiocytosis, Langerhans-Cell*
Humans
Langerhans Cells
Lymphatic Diseases
Prednisone
Purpura
Tennis
Vincristine
Cyclophosphamide
Etoposide
Prednisone
Vincristine
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