FIBRODYSPLASIA OSSIFICANS PROGRESSIVA: CASE REPORT

Main Article Content

Ummara Siddique Umer
Zeeshan Khan
Aman Nawaz Khan
Shahjehan Alam
Syed Ghulam Ghaus
Seema Gul
Hina Gul
Rabia Afridi

Abstract

Fibrodysplasia ossificans progressiva is a very rare inherited connective tissue disease characterized by progressive heterotopic ossification in soft tissues of the trunk and extremities with associated congenital malformation of great toes and thumbs. Episodic flare-ups of pre-osseous soft tissue swelling usually begins during early childhood and progress throughout life causing progressive ankylosis of joints with resultant severe disability. Literature review reveals that there are more than 600 reported cases so far and presently there is no prevention or effective treatment for this disorder. Imaging plays a major role in the diagnosis to prevent unnecessary harmful biopsies. We present a case of a 2-year-old boy with extensive heterotopic ossification with classical radiological findings.

Article Details

How to Cite
1.
Siddique Umer U, Khan Z, Khan AN, Alam S, Ghaus SG, Gul S, Gul H, Afridi R. FIBRODYSPLASIA OSSIFICANS PROGRESSIVA: CASE REPORT. J Postgrad Med Inst [Internet]. 2018 Nov. 28 [cited 2021 Oct. 16];32(4). Available from: https://jpmi.org.pk/index.php/jpmi/article/view/2353
Section
Case Report
Author Biographies

Ummara Siddique Umer

Assistant Professor

Radiology Department

Rehman Medical Institute Peshawar

Zeeshan Khan, Rehman Medical Institute Peshawar

Orthopedic Surgeon RMI

Aman Nawaz Khan, Rehman Medical Institute Peshawar

Interventional Radiologist

Shahjehan Alam, Rehman Medical Institute Peshawar

Associate Professor Radiology

Syed Ghulam Ghaus, Rehman Medical Institute Peshawar

Associate Professor Radiology

Seema Gul, Rehman Medical Institute Peshawar

Associate Professor Radiology

Hina Gul, Khyber Teaching Hospital Peshawar

Associate Professor Radiology

Rabia Afridi, Rehman Medical Institute Peshawar

Senior Sonologist

Most read articles by the same author(s)

1 2 > >>