medigraphic.com
SPANISH

Revista Mexicana de Ortopedia Pediátrica

ISSN 2007-087X (Print)
Órgano Oficial de la Sociedad Mexicana de Ortopedia Pediátrica
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2010, Number 1

<< Back Next >>

Rev Mex Ortop Ped 2010; 12 (1)

Histiocitosis en cadera derecha, reporte de un caso

Macías-León JP, Meza-Vernis A, Isunza-Ramírez A
Full text How to cite this article

Language: Spanish
References: 15
Page: 43-47
PDF size: 226.24 Kb.


Key words:

Langerhans cell histiocytosis, hip.

ABSTRACT

Objective: Langerhans cells histiocytosis presents in the pelvis in 10% of all cases, in the hip there are only a few cases reported. Material and methods: A 7 year old girl, with a history of septic arthritis in the right hip presented with a limp, and shortening of the limb by 1cm Range of motion was limited and there was significant muscle wasting but otherwise shewas in good health. Results: Alkaline phosphatase was 481, radiologically with a subluxation of the right hip, the X rays had mirror image and mouse bite like images, which suggested osteoarticular granulomatose tuberculosis or a bone neoplasia. Biopsies where performed, and reported Langerhans cell histiocytosis. An adductor and psoas tenotomy was performed, and the limb length discrepancy was treated with a lift. The patient is currently asymptomatic. Conclusions: The incidence of Langerhans cell histiocytosis in the hip is very rare, but should be considered in the differential diagnosis of neoplastic disease of the hip.
Level of evidence: IV


REFERENCES

  1. Egeler RM, D’Angio GJ. Langerhans cell histiocytosis. J Pediatr 1995; 127: 1-11

  2. Favara BE, Feller AC, Pauli M. Contemporary classification of histiocytic disorders. Med Pediatr Oncol 1997; 29: 157-166.

  3. Berry DH, Gresik MV, Humphrey GB et al. Natural history of histiocytosis X: a pediatric oncology group study. Med Pediatr Oncol 1986; 14: 1-5.

  4. Meyer JS, Harty MP, Mahboubi S et al. Langerhans cell histiocytosis: presentation and evolution of radiologic findings with clinical correlation. Radiographics 1995; 15: 1135-1146.

  5. Chu T, Jaffe R. The normal Langerhans cell and the LCH cell. Br J Cancer 1994; 70 (suppl 23): S4-S10.

  6. Webb DKH. Histiocytic syndromes. En: Lilleyman J, Hann I, Blanchette V (eds) Pediatric Hematology, 2nd ed. Churchill Livingstone, London, 1999: 356-361.

  7. Willman CL. Detection of clonal histiocytes in Langerhans cell histiocytosis: biology and clinical significance. Br J Cancer 1994; 23: S29-S33.

  8. Stull MA, Kransdorf MJ, Devaney KO. Langerhans cell histiocytosis of bone. Radiographics 1992; 12: 801-823.

  9. Hutchinson RE, Uner AH. Pediatric neoplasia. Morphology and biology. In: Parham DM (ed). Tumors of the lymphoid organs. Lippincott - Raven, Philadelphia, 1996: 519-521.

  10. Azouz EM, Sargal G, Rodríguez MM, Podda A. Langerhans cell histiocytosis: pathology, imaging and treatment of skeletal involvement. Pediatr Radiol 2005; 35: 103-115.

  11. Fernandez-Latorre F, Menor-Serrano F, Alonso Charterina S, et al. Langerhans cell histiocytosis of the temporal bone in pediatric patients: imaging and follow-up. Am J Roentgenol AJR 2000; 174: 217-221.

  12. Ugarriza FL, Cabezudo JM, Porras LF et al. Solitary eosinophilic granuloma of the cervicothoracic junction causing neurological deficit. Br J Neurosurg 2003; 17: 178-181.

  13. Jabra AA, Fisherman EK. Eosinophilic granuloma simulating an aggressive rib neoplasm: CT evaluation. Pediatr Radiol 1992; 22: 447-448.

  14. Sartorio DJ, Parker BR. Histiocytosis X: rate and pattern of resolution of osseous lesions. Radiology 1984; 152: 679-684.

  15. Conway JJ. Commentary. Pediatr Radiol 1996; 26: 742-743.




2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Rev Mex Ortop Ped. 2010;12