scholarly journals Fibrocartilaginous Dysplasia of the Bone: A Rare Variant of Fibrous Dysplasia

Cureus ◽  
2016 ◽  
Author(s):  
Raju Vaishya ◽  
Amit Kumar Agarwal ◽  
Nishint Gupta ◽  
Vipul Vijay
2021 ◽  
Vol 6 (3) ◽  
pp. 222-224
Author(s):  
Shilpa Mishra ◽  
Rakesh Rajiv Patkar ◽  
Amrita Neelakantan

Fibrocartilaginous dysplasia (FCD) or massive cartilaginous differentiation in fibrous dysplasia are interchangeably used terms. It is a rare variant of fibrous dysplasia (FD) which is benign, lytic, and expansile bone lesion and causes progressive deformity in the bones and may lead to pathological fracture. Radiologically, FCD may confused with cartilaginous benign and malignant bone tumours. FCD usually shows calcification in imaging. Surgical curettage or corrective osteotomy and histopathological examination of these lesions is necessary to differentiate it from other cartilaginous tumours. Here we report case of fibrocartilaginous dysplasia of distal femur in a 4-year-old male child.


2016 ◽  
Vol 9 (1) ◽  
pp. 126-133 ◽  
Author(s):  
Hideo Morioka ◽  
Yasuhiro Kamata ◽  
Kazumasa Nishimoto ◽  
Michiro Susa ◽  
Kazutaka Kikuta ◽  
...  

Fibrous dysplasia (FD) is a monostotic or polyostotic benign bone lesion with spindle-cell proliferation in woven bone and stroma. Rarely, cartilaginous differentiation can be seen in the lesions of FD. FD with massive cartilaginous differentiation is called fibrocartilaginous dysplasia (FCD) and is considered a rare variant of FD. Although pathological findings of FD show irregular immature bone formation without osteoblastic rimming in fibrous tissue, and rarely show very small amounts of cartilage, histological images of FCD are said to show that cartilage with a relatively high cell density is present in the majority and that FD-like findings are seen in parts of it. The most characteristic feature of FCD on images is calcification in the lesions reflecting cartilaginous tissue. On the other hand, typical radiographic findings of FD include shadows with a ground-glass appearance and thinning and bulging of the cortical bone, the observation if calcification is not usual. Therefore, in the diagnosis of FCD, differentiation from multiple enchondromatosis, Ollier disease, chondrosarcoma, and chondrosarcoma secondary to FD is necessary, and it seems important to make a careful diagnosis based not only on the pathological findings but also on imaging and clinical findings. Herein, we report on a case of FD of the proximal femur associated with intralesional extensive cartilaginous differentiation in which a pathological fracture occurred during follow-up, with a review of the literature.


2014 ◽  
Vol 15 (1) ◽  
pp. 156 ◽  
Author(s):  
Manzoor Ahmed ◽  
Phillip Daniel Knott

2007 ◽  
Vol 36 (6) ◽  
pp. 523-529 ◽  
Author(s):  
Makoto Endo ◽  
Akira Kawai ◽  
Eisuke Kobayashi ◽  
Yuki Morimoto ◽  
Umio Yamaguchi ◽  
...  

2015 ◽  
Vol 3 (1) ◽  
pp. 37
Author(s):  
HL Kishan Prasad ◽  
Netra Sajjan ◽  
Lawrence Mathias ◽  
KJayaprakash Shetty ◽  
Chandrika Rao ◽  
...  

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