The langerhans cell histiocytosis X files revealed

British Journal of Haematology

Volumn 116, Issue 1, 2002, Pages 3-9

  Coppes Zantinga, Arty ^a   Egeler, R Maarten ^a,b  

^a UNIVERSITY OF CALGARY   (Canada)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Histiocytosis X; History; Langerhans cell histiocytosis

Indexed keywords

ABT LETTERER SIWE DISEASE; CELL PROLIFERATION; CLINICAL FEATURE; DISEASE COURSE; EOSINOPHILIC GRANULOMA; HISTIOCYTOSIS X; HUMAN; LANGERHANS CELL; LIFE EVENT; MEDICAL INFORMATION; PHYSICIAN; PRIORITY JOURNAL; PUBLICATION; REVIEW;

HISTIOCYTOSIS, LANGERHANS-CELL; HISTORY, 19TH CENTURY; HISTORY, 20TH CENTURY; HUMANS; PORTRAITS;

EID: 0036164540     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2002.03232.x     Document Type: Review

References (47)

1. Letterer-Siwe's disease; splenohepatomegaly, associated with widespread hyperplasia of non lipoid-storing macrophages; discussion of the so-called reticuloendotheliosis
2. Familial clustering of Langerhans cell histiocytosis
3. Das reticulo-endotheliale system
4. Cytogenetic abnormalities in Langerhans cell histiocytosis
5. An electron microscope study of basal melanocytes and high-level clear cells (Langerhans cells) in vitiligo
6. Histiocytosis syndromes in children: II. Approach to the clinical and laboratory evaluation of children with Langerhans cell histiocytosis
7. Defects in membranous bones, exophthalmos and diabetes insipidus: An unusual syndrome of dyspituitarism
8. Histiocytosis syndromes in children
9. The primary reticulo-endothelial granulomas with report of an atypical case of Letterer-Siwe's disease
10. Medical Progress: Langerhans cell histiocytosis
11. Langerhans cell histiocytosis and other disorders of monocyte-histiocyte lineage
12. Paul Langerhans Jr (1847-1888): A short life, yet two eponymic legacies
13. Differential in situ cytokine profiles of Langerhans-like cells and T-cells in Langerhans cell histiocytosis: Abundant expression of cytokines relevant to disease and treatment
14. Abundant expression of CD40 and CD40-ligand (CD154) in paediatric Langerhans cell histiocytosis lesions
15. The nature of "Solitary or Eosinophilic Granuloma" of bone
16. Skeletal lipoid granulomatosis (Hand-Schüller-Christian's disease)
17. A randomized trial of treatment for multisystem Langerhans' cell histiocytosis
18. Differentiation of Langerhans cells in Langerhans cell histiocytosis
19. 'Eosinophilic or Solitary Ganuloma' of bone
20. Polyuria and tuberculosis
21. Defects of membranous bones, exophthalmos and polyuria in childhood: Is it dyspituitarism?
22. Paul Langerhans, Life and Work Part I, II, III
23. Eosinophilic granuloma of bone. A condition affecting one, several or many bones, but apparently limited to the skeleton, and representing the mildest clinical expression of the peculiar inflammatory histiocytosis also underlying Letterer-Siwe disease and Schuller-Christian disease
24. Acquired hydrocephalus with atrophic bone changes, exophthalmos, and polyuria (with presentation of the patient)
25. Historical perspectives of Langerhans cell histiocytosis
26. A randomized trial of etoposide vs. vinblastine in disseminated Langerhans cell histiocytosis
27. Uber die nerven der menslichen haut
28. Berichtingungen (u.a. zu den nervenenden der haut, und nervenfasern im rete)
29. Aleukamische retikulose (ein beitrag zu den proliferativen erkrankungen des retikuloendothelialapparates)
30. Histiocytosis X: Integration of eosinophilic granuloma of bone, Letterer-Siwe disease and Schuller-Christian disease as related manifestations of a single nosologic entity
31. Histiocytosis X (eosinophilic granuloma of bone, Letterer-Siwe disease, and Schuller-Christian disease
32. Eosinophilic granuloma of bone
33. Ein granulationstumor des stirnbeins
34. Lichtenstein L.
35. Langerhans cell histiocytosis research. Past, present, and future
36. Histiocytosis X: Histogenic arguments for a Langerhans' cell orgin
37. Solitary granuloma of bone, simulating primary neoplasm
38. Reticulogranuloma: Report of a case of eosinophilic granuloma of bone associated with nonlipid reticulosis of skin and oral mucosa under the clinical picture of Hand-Schuller-Christian disease
39. Histiocytosis X (Langerhans' cell histiocytosis). Prognostic role of histopathology
40. Cytogenetic abnormalities in PHA-stimulated lymphocytes from patients with Langerhans cell histocytosis
41. Uber eigenartige schadeldefekte im jugendalter
42. Die reticuloendotheliose - Ein neues krankheitsbild unter den hepatosplenomegalien
43. Skull cap showing congenital deficiency of bone
44. Evidence that Langerhans cells in adult pulmonary Langerhans cell histiocytosis are mature dendritic cells: Importance of the cytokine microenvironment
45. Langerhans' cell histiocytosis (histiocytosis X) - Aclonal proliferatice disease