Sclerosing bone dys-plasias: Review and differentiation from other causes of osteosclerosis

Radiographics

Volumn 31, Issue 7, 2011, Pages 1865-1882

  Ihde, Lauren L ^a   Forrester, Deborah M ^a   Gottsegen, Christopher J ^a   Masih, Sulabha ^b   Patel, Dakshesh B ^a   Vachon, Linda A ^a   White, Eric A ^a   Matcuk, George R ^a  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE DYSPLASIA; DIAGNOSTIC IMAGING; DIFFERENTIAL DIAGNOSIS; HUMAN; METHODOLOGY; OSTEOSCLEROSIS; REVIEW;

BONE DISEASES, DEVELOPMENTAL; DIAGNOSIS, DIFFERENTIAL; DIAGNOSTIC IMAGING; HUMANS; OSTEOSCLEROSIS;

EID: 81255136563     PISSN: 02715333     EISSN: 15271323     Source Type: Journal    
DOI: 10.1148/rg.317115093     Document Type: Article

References (21)

1. Vanhoenacker FM, De Beuckeleer LH, Van Hul W, et al. Sclerosing bone dysplasias: genetic and radio-clinical features. Eur Radiol 2000;10(9):1423-1433.
2. Greenspan A. Sclerosing bone dysplasias: a target-site approach. Skeletal Radiol 1991;20(8):561-583.
3. de Vernejoul MC. Sclerosing bone disorders. Best Pract Res Clin Rheumatol 2008;22(1):71-83.
4. Van Hul W. Lessons from sclerosing bone dysplasias. Horm Res 2007;68(suppl 5):37-39.
5. Beighton P, Hamersma H. The orthopaedic implications of the sclerosing bone dysplasias. S Afr Med J 1980;58(15):600-604.
6. Viot G, Lacombe D, David A, et al. Osteopathia striata cranial sclerosis: non-random X-inactivation suggestive of X-linked dominant inheritance. Am J Med Genet 2002;107(1):1-4.
7. Kinoshita A, Saito T, Tomita H, et al. Domain-specifc mutations in TGFB1 result in Camurati-Engelmann disease. Nat Genet 2000;26(1):19-20.
8. Janssens K, Gershoni-Baruch R, Guañabens N, et al. Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-En-gelmann disease. Nat Genet 2000;26(3):273-275.
9. Janssens K, ten Dijke P, Ralston SH, Bergmann C, Van Hul W. Transforming growth factor-beta 1 mutations in Camurati-Engelmann disease lead to increased signaling by altering either activation or secretion of the mutant protein. J Biol Chem 2003; 278(9):7718-7724.
10. Naveh Y, Kaftori JK, Alon U, Ben-David J, Berant M. Progressive diaphyseal dysplasia: genetics and clinical and radiologic manifestations. Pediatrics 1984;74(3):399-405.
11. Neuhauser EB, Shwachman H, Wittenborg M, et al. Progressive diaphyseal dysplasia. Radiology 1948;51 (1):11-22.
12. Hundley JD, Wilson FC. Progessive diaphyseal dys-plasia: review of the literature and report of seven cases in one family. J Bone Joint Surg Am 1973;55 (3):461-474.
13. Seeger LL, Hewel KC, Yao L, et al. Ribbing disease (multiple diaphyseal sclerosis): imaging and differential diagnosis. AJR Am J Roentgenol 1996;167(3): 689-694.
14. Makita Y, Nishimura G, Ikegawa S, Ishii T, Ito Y, Okuno A. Intrafamilial phenotypic variability in Engelmann disease (ED): are ED and Ribbing disease the same entity? Am J Med Genet 2000;91(2): 153-156.
15. Ribbing S. Hereditary, multiple, diaphyseal sclerosis. Acta Radiol 1949;31(5-6):522-536.
16. Paul LW. Hereditary multiple diaphyseal sclerosis (ribbing). Radiology 1953;60(3):412-416.
17. Chanchairujira K, Chung CB, Lai YM, Haghighi P, Resnick D. Intramedullary osteosclerosis: imaging features in nine patients. Radiology 2001;220(1): 225-230.
18. Smith SE, Murphey MD, Motamedi K, Mulligan ME, Resnik CS, Gannon FH. Radiologic spectrum of Paget disease of bone and its complications with pathologic correlation. RadioGraphics 2002;22(5): 1191-1216.
19. Dion E, Graef C, Miquel A, et al. Bone involvement in Erdheim-Chester disease: imaging fndings including periostitis and partial epiphyseal involvement. Radiology 2006;238(2):632-639.
20. Guermazi A, de Kerviler E, Cazals-Hatem D, Zag-danski AM, Frija J. Imaging fndings in patients with myelofbrosis. Eur Radiol 1999;9(7):1366-1375.
21. Ejindu VC, Hine AL, Mashayekhi M, Shorvon PJ, Misra RR. Musculoskeletal manifestations of sickle cell disease. RadioGraphics 2007;27(4):1005-1021.