IJHSR

International Journal of Health Sciences and Research

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Case Report

Year: 2020 | Month: October | Volume: 10 | Issue: 10 | Pages: 102-104

Osteofibrous Dysplasia: A Rare Case Involving Humerus

Gargi Gupta1, Reeta Dhar2, Shilpi Sahu3

1Post-graduate Student, 2Professor, 3Professor and HOD,
Department of Pathology, MGM’s Medical College and Hospital, Navi Mumbai.

Corresponding Author: Reeta Dhar

ABSTRACT

Osteofibrous dysplasia (OFD) is a benign fibro-osseous lesion in cortical bone of anterior mid-shaft of the tibia of infancy and childhood. The lesion is characterized by slow growth and proliferation of fibrous cellular tissue, bone, cement or in combination. A 49 years old male came to tertiary care centre with history of swelling on left arm since one month associated with pain and was gradually progressive. History of intramuscular injection and diabetes was present. Clinical diagnosis of deltoid granuloma on left lateral aspect of deltoid on upper arm was made.
Case History: A 49 years old male came to tertiary care centre, Navi Mumbai with history of gradually progressive swelling on left arm since one month associated with pain. Patient gave history of intramuscular injection in the past. History of Diabetes was also there. Clinical diagnosis of deltoid granuloma was made.
Conclusion: We reported an extremely rare case of Osteofibrous dysplasia arising in an adult in humerus and cortical excision from left lateral aspect of upper arm was given. It is important to recognize OFD clinically for further timely and appropriate treatment.

Key words: Fibro-osseous lesion, deltoid, ossifying fibroma.

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