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Lichtenstein, L. (1953) Histiocytosis X: Integration of eosinophilic granuloma of bone, letterer-siwe disease and schuller-christian disease as related manifestations of a single nosologic entity. AMA Archives of Pathology, 56, 84-102.

has been cited by the following article:

• TITLE: Thymic langerhans cell histiocytosis in children: A case report

  AUTHORS: Marie Poncelet, Camille Chabert, Jean Pierre Pracros, Perrine Marec Berard

  KEYWORDS: Langerhans Cell Histiocytosis; Children; Thymus

  JOURNAL NAME: Open Journal of Pediatrics, Vol.2 No.4, December 13, 2012

  ABSTRACT: Langerhans cell histiocytosis has long been described as a rare systemic disorder involving the proliferation of Langerhans cells with formation of granuloma. The disease may be localised or diffuse. Typical forms of the disease involving the bone, the skin or the pituitary gland have been well described whereas others, such as thymic histiocytosis, are still poorly understood. Here, we report a case of isolated Langerhans cell histiocytosis of the thymus in an infant with non-specific symptoms. We provide a description of the disease and discuss patient management.