Histiocytosis, sickle cell anemia, and rhabdomyosarcoma

Romaine F Johnson, Shyan Vijayasekaran, Charles M. Myer

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Langerhans cell histiocytosis (LCH) is a hemopoietic disorder that can affect single or multiple sites simultaneously. It is a disorder that affects mostly children. The clinical course is variable and can range from isolated disease that resolves spontaneously to systemic disease that is rapidly progressive and lethal.

Original languageEnglish (US)
Title of host publicationHead and Neck Manifestations of Systemic Disease
PublisherCRC Press
Pages285-296
Number of pages12
ISBN (Electronic)9781420017564
ISBN (Print)9780849340505
StatePublished - Jan 1 2007

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Histiocytosis
Rhabdomyosarcoma
Sickle Cell Anemia
Langerhans Cell Histiocytosis

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Johnson, R. F., Vijayasekaran, S., & Myer, C. M. (2007). Histiocytosis, sickle cell anemia, and rhabdomyosarcoma. In Head and Neck Manifestations of Systemic Disease (pp. 285-296). CRC Press.

Histiocytosis, sickle cell anemia, and rhabdomyosarcoma. / Johnson, Romaine F; Vijayasekaran, Shyan; Myer, Charles M.

Head and Neck Manifestations of Systemic Disease. CRC Press, 2007. p. 285-296.

Research output: Chapter in Book/Report/Conference proceedingChapter

Johnson, RF, Vijayasekaran, S & Myer, CM 2007, Histiocytosis, sickle cell anemia, and rhabdomyosarcoma. in Head and Neck Manifestations of Systemic Disease. CRC Press, pp. 285-296.
Johnson RF, Vijayasekaran S, Myer CM. Histiocytosis, sickle cell anemia, and rhabdomyosarcoma. In Head and Neck Manifestations of Systemic Disease. CRC Press. 2007. p. 285-296
Johnson, Romaine F ; Vijayasekaran, Shyan ; Myer, Charles M. / Histiocytosis, sickle cell anemia, and rhabdomyosarcoma. Head and Neck Manifestations of Systemic Disease. CRC Press, 2007. pp. 285-296
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