Korean J Otolaryngol-Head Neck Surg.  2001 Feb;44(2):206-208.

A case of Langerhans cell histiocytosis of bilateral temporal bone

Affiliations
  • 1Department of Otolaryngology, Medical School, Chonnam National University Kwangju, Korea.

Abstract

Langerhans cell histiocytosis refers to a group of disorders of the reticuloendothelial system which is characterized by a proliferation of histiocytes and includes eosinophilic granuloma, Letterer-Siwe diseases, and Hand-Schuller Christian disease. It may involve the femur, pelivis, scapulae, vertebrae, ribs, mandible, maxilla, skull including the temporal bone, and skin, lymph node, viscera. The severity of these diseases and their prognosis and treatments differ greatly. We have experienced a case of Langerhans cell histiocytosis in 2 year old male with bilateral temporal bone involvement. We report it with the review of literature.

Keyword

Langerhans cell histiocytosis; Temporal bone

MeSH Terms

Child, Preschool
Eosinophilic Granuloma
Femur
Histiocytes
Histiocytosis, Langerhans-Cell*
Humans
Lymph Nodes
Male
Mandible
Maxilla
Mononuclear Phagocyte System
Prognosis
Ribs
Scapula
Skin
Skull
Spine
Temporal Bone*
Viscera
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