Ollier Disease: A Case Report and Literature Review
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Abstract
Ollier disease is an uncommon disease characterized by several enchondromas and an asymmetric distribution of cartilage lesions, which can vary significantly in size, location, age, and gender. The primary symptom of this condition is a nonossifying chondrocyte mass or hamartomatous chondrocyte growth in the metaphysis of a short or long bone. Specific cases can progress to chondrosarcoma or osteosarcoma. X-ray is the most fundamental diagnostic technique for skeletal illnesses. In this article, we present a case of Ollier disease from Mother and Child Hospital IBN SINA, Rabat, Morocco.
References
1.
Murphey M, Flemming D, Boyea S, Bojescul J, Sweet D, Temple H
. Enchondroma versus chondrosarcoma in the appendicular skeleton: differentiating features. Radiographics. 1998; 18(5):1213-37; quiz 1244-5.
DOI: 10.1148/radiographics.18.5.9747616.
View
2.
Amary M, Damato S, Halai D, Eskandarpour M, Berisha F, Bonar F
. Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2. Nat Genet. 2011; 43(12):1262-5.
DOI: 10.1038/ng.994.
View
3.
Kumar A, Jain V, Bharadwaj M, Arya R
. Ollier Disease: Pathogenesis, Diagnosis, and Management. Orthopedics. 2015; 38(6):e497-506.
DOI: 10.3928/01477447-20150603-58.
View
4.
Jacobi C, Hiranya E, Gay A, Holzmann D, Kollias S, Soyka M
. Enchondroma of the nasal septum due to Ollier disease: a case report and review of the literature. Head Neck. 2014; 37(3):E30-3.
DOI: 10.1002/hed.23783.
View
5.
El Abiad J, Robbins S, Cohen B, Levin A, Valle D, Morris C
. Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature. Am J Med Genet A. 2020; 182(5):1093-1103.
PMC: 8164175.
DOI: 10.1002/ajmg.a.61530.
View