- ►hematologylibrary.org - Free from Publisher F Braiteh, C Boxrud, B Esmaeli, R Kurzrock - Blood, 2005 - bloodjournal.hematologylibrary.org Erdheim-Chester disease is a rare non-Langerhans histiocytosis with multisystem
involvement. To date, there is no standard treatment for this disorder, and more
than half of the patients succumb within 3 years. Because interferon- ... Cited by 30 - Related articles - BL Direct - All 4 versions
J Haroche, Z Amoura, SG Trad, B Wechsler, P … - Arthritis Care & Research - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 23 - Related articles - BL Direct - All 3 versions
A Stoppacciaro, M Ferrarini, C Salmaggi, C … - Arthritis Care & Research - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 7 - Related articles - BL Direct - All 3 versions
- ►nih.gov JA Sivak-Callcott, J Rootman, SL Rasmussen, … - British Medical Journal, 2006 - bjo.bmj.com Results: 137 cases were compiled. There was no sex or age difference between
syndromes. AOX, AAPOX, NBX affect the anterior orbit, ECD tends to be diffuse
and intraconal. Skin lesions are found in all the syndromes. Immune ... Cited by 6 - Related articles - BL Direct - All 8 versions
RC Miller, S Villà, S Kamer, D Pasquier, P … - Radiotherapy and Oncology, 2006 - Elsevier Erdheim–Chester disease (ECD) is an uncommon non-Langerhans cell histiocytosis
characterized by symmetric sclerotic radiologic changes of the long bones and
histiocytic infiltration of several organ systems with lipid-laden ... Cited by 2 - Related articles - All 18 versions
MA Ozdemir, A Coşkun, YA Torun, O Canoz, A … - Journal of neuro-oncology, 2007 - ncbi.nlm.nih.gov Erdheim-Chester disease (ECD) is a systemic histiocytic disorder that occurs
mainly in adults and is rarely found in children. Age at diagnosis ranges from 7
to 84 years (mean age, 53 years) with a female-to-male ratio of 3:1. ECD is ... Cited by 1 - Related articles - All 2 versions
T Srikulmontree, HD Massey, WN Roberts - Rheumatology International, 2007 - Springer Abstract Erdheim–Chester disease (ECD) is a rare non-Langerhans cell
histiocytosis characterized by tis- sue inWltration of lipid-laden macrophages,
multinucle- ated giant cells, and inXammatory inWltrate of lymphocytes and ... Cited by 1 - Related articles - BL Direct - All 3 versions
A Mounach, A Nouijai, L Achemlal, A El … - Rheumatology International - Springer Abstract We report the case of a 42-year-old woman who was admitted in 2002 for
exploration of diffuse bone pain. She had medical history of pulmonary
tuberculosis. Her current symptoms had started 9 months earlier and ... Related articles - All 2 versions
AN Bugnone, HT Temple, S Humble - Clinical orthopaedics and related research, 2006 - journals.lww.com From the *Department of Radiology, the †Department of Orthopedics and
Rehabilitation, and the ‡Department of Pathology, University of Miami School
of Medicine, Miami, Florida. Each author certifies that he or she has no ... Related articles - BL Direct - All 3 versions
A Aouba, F Larousserie, V Le Guern, A Martin, … - Joint Bone Spine, 2009 - Elsevier A 27-year-old man consulted with clinical and radiological features of chronic
erosive oligoarthritis of large joints (hips and knee), associated with diffuse
lymph-node enlargement and diabetes insipidus. Lymph-node biopsy provided ... Related articles - All 2 versions