Histiocytosis X SOA Textbook (Visit this link)
Histiocytosis X (Lichtenstein 1977) or Langerhan's Cell histiocytosis (Bergholz 1979), is the currently favored term, for a spectrum of granulomatous conditions characterized by proliferating histiocytic cells admixed with eosinophils and other inflammatory cells.
The purpose of this chapter is to familiarize the reader with the spectrum of conditions encompassed under the broad designation of Histiocytosis X, with a recommended plan of management for each condition. Emphasis will be given to discussion and management of the condition most commonly referred to as Eosinophilic Granuloma.
John L. Eady, MD, FACS Courtney Gleason
University of South Carolina School of Medicine
Columbia, SC
Outline - I. Introduction
II. Historical Perspective
III. Anatomic and Physciologic Considerations
IV. Natural History and Classifications
V. Diagnosis and Recognition
Clinical Presentation
Radiographic Findings
Gross and Microscopic Appearance
Differential Diagnosis
VI. Treatment
Methods of Management
Spine
Pelvis
Sacral
Long Tubular Weight Bearing Bones (femur, tibia, humerus)
VII. Summary
X. References
XI. Patient Education Summary
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