scholarly journals Osteofibrous dysplasia-like adamantinoma versus osteofibrous dysplasia in children: A case report of challenging diagnosis

2021 ◽  
Vol 80 ◽  
pp. 105599
Author(s):  
Achmad Fauzi Kamal ◽  
Fahmi Anshori ◽  
Evelina Kodrat
2021 ◽  
Vol 28 ◽  
pp. 221049172110258
Author(s):  
Weiguo Li ◽  
Ka-Lok Mak ◽  
Tsz W Yau ◽  
Tit L Lam ◽  
Chak L Chan ◽  
...  

A five-year-old boy presented with left tibial swelling; there was a typical radiological feature of osteofibrous dysplasia. He was observed until the age of 14 years; there was development of aggressive radiological features. Biopsy revealed chondroblastic osteosarcoma. It was excised and the histology revealed chondroblastic osteosarcoma. A small lesion distal to the main tumour revealed adamantinoma within a background of feature of osteofibrous dysplasia. Proximally, feature of osteofibrous dysplasia was identified focally. The finding of adamantinoma over the distal part of the lesion supports that feature of osteofibrous dysplasia may be a precursor of adamantinoma. They may be a spectrum of diseases with multistep neoplastic transformation. The osteosarcoma may be a result of de-differentiation from adamantinoma. This case is remarkable as the patient was only 14 years old and the tumour showed typical features of osteosarcoma, with feature of osteofibrous dysplasia and adamantinoma found in the same specimen. Feature of osteofibrous dysplasia may be a precursor of adamantinoma, and adamantinoma may dedifferentiate into osteosarcoma.


2016 ◽  
Vol 146 (suppl_1) ◽  
Author(s):  
Arslan Ahmad ◽  
Chuanyong Lu ◽  
Carmencita Yudis ◽  
Vincent Vigorita

1984 ◽  
Vol 82 (4) ◽  
pp. 470-474 ◽  
Author(s):  
Antonio Alguacil-Garcia ◽  
Ana Alonso ◽  
Norman M. Pettigrew

2015 ◽  
Vol 2 (31) ◽  
pp. 4663-4665
Author(s):  
Sujata S Giriyan ◽  
Parvathi S Jigalur ◽  
Anita Karani

Sarcoma ◽  
2004 ◽  
Vol 8 (1) ◽  
pp. 51-56 ◽  
Author(s):  
Eitan Segev ◽  
Josephine Issakov ◽  
Eli Ezra ◽  
Shlomo Wientroub ◽  
Itzchak Meller

We present a case of giant osteofibrous dysplasia (OFB) of the proximal tibia with 15 years of follow-up. The tumor recurred after first biopsy and curettage done at the age of 6 years and, again, 4 years later. Following recurrence, the option of amputation was suggested. Staged treatment of curettage, cryosurgery, bone cement as a temporary spacer with internal fixation at age 12 years, followed by bone grafting at age 14 years, led to complete healing. The staged protocol for treatment is proposed as an alternative to more radical solutions. It is suggested to postpone surgical treatment towards skeletal maturity.


2020 ◽  
Vol 8 (10) ◽  
pp. 901-903
Author(s):  
Jalal H ◽  
Mortaji H ◽  
Alami Y ◽  
Basraoui D ◽  
Mouhtadi A ◽  
...  

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