Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification
Fibrodysplasia ossificans progressiva (FOP) is an exceptionally rare genetic disorder characterized by the progressive formation of heterotopic bone in soft tissues. Here, we present the radiological findings of an 18-year-old female diagnosed with FOP who had severe spinal and right-upper-limb abno...
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sg-ntu-dr.10356-1694922024-05-03T00:29:37Z Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification Mohammed Mostafa Kotb Omar, Usama Farghaly Kaliya-Perumal, Arun-Kumar Lee Kong Chian School of Medicine (LKCMedicine) Medicine, Health and Life Sciences Fibrodysplasia ossificans progressiva Heterotopic ossification Fibrodysplasia ossificans progressiva (FOP) is an exceptionally rare genetic disorder characterized by the progressive formation of heterotopic bone in soft tissues. Here, we present the radiological findings of an 18-year-old female diagnosed with FOP who had severe spinal and right-upper-limb abnormalities. Her SF-36 scores suggested significant impairment in physical function, affecting work and other regular daily activities. Radiographic evaluation with X-rays and CT scans revealed scoliosis and total fusion of almost all levels of the spine, with only a few disc spaces spared. A large mass of heterotopic bone was observed, corresponding to the location of the paraspinal muscles in the lumbar region, branching upwards and fusing with the scapulae on both sides. On the right side, this exuberant heterotopic bone mass fused with the humerus, resulting in a fixed right shoulder, while the rest of the upper and lower limbs are spared and have a range of motion. Our report highlights the extensive ossification that can manifest in patients with FOP, resulting in restricted mobility and a poor quality of life. While there is no definite treatment that can reverse the effects of the disease, preventing injuries and minimizing iatrogenic harm is of critical importance in this patient as inflammation is known to play a key role in triggering heterotopic bone. Meanwhile, ongoing research into therapeutic strategies holds the key to unlocking a potential cure for FOP in the future. Published version 2023-07-20T05:11:36Z 2023-07-20T05:11:36Z 2023 Journal Article Mohammed Mostafa Kotb, Usama Farghaly Omar & Arun-Kumar Kaliya-Perumal (2023). Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification. Diagnostics, 13(10), 1711-. https://dx.doi.org/10.3390/diagnostics13101711 2075-4418 https://hdl.handle.net/10356/169492 10.3390/diagnostics13101711 37238196 2-s2.0-85160512955 https://www.mdpi.com/2075-4418/13/10/1711 10 13 1711 en Diagnostics © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). application/pdf |
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Medicine, Health and Life Sciences Fibrodysplasia ossificans progressiva Heterotopic ossification Mohammed Mostafa Kotb Omar, Usama Farghaly Kaliya-Perumal, Arun-Kumar Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification |
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Fibrodysplasia ossificans progressiva (FOP) is an exceptionally rare genetic disorder characterized by the progressive formation of heterotopic bone in soft tissues. Here, we present the radiological findings of an 18-year-old female diagnosed with FOP who had severe spinal and right-upper-limb abnormalities. Her SF-36 scores suggested significant impairment in physical function, affecting work and other regular daily activities. Radiographic evaluation with X-rays and CT scans revealed scoliosis and total fusion of almost all levels of the spine, with only a few disc spaces spared. A large mass of heterotopic bone was observed, corresponding to the location of the paraspinal muscles in the lumbar region, branching upwards and fusing with the scapulae on both sides. On the right side, this exuberant heterotopic bone mass fused with the humerus, resulting in a fixed right shoulder, while the rest of the upper and lower limbs are spared and have a range of motion. Our report highlights the extensive ossification that can manifest in patients with FOP, resulting in restricted mobility and a poor quality of life. While there is no definite treatment that can reverse the effects of the disease, preventing injuries and minimizing iatrogenic harm is of critical importance in this patient as inflammation is known to play a key role in triggering heterotopic bone. Meanwhile, ongoing research into therapeutic strategies holds the key to unlocking a potential cure for FOP in the future. |
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Lee Kong Chian School of Medicine (LKCMedicine) |
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Lee Kong Chian School of Medicine (LKCMedicine) Mohammed Mostafa Kotb Omar, Usama Farghaly Kaliya-Perumal, Arun-Kumar |
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Article |
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Mohammed Mostafa Kotb Omar, Usama Farghaly Kaliya-Perumal, Arun-Kumar |
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Mohammed Mostafa Kotb |
title |
Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification |
title_short |
Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification |
title_full |
Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification |
title_fullStr |
Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification |
title_full_unstemmed |
Living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification |
title_sort |
living with fibrodysplasia ossificans progressiva: radiological images of a patient with extensive heterotopic ossification |
publishDate |
2023 |
url |
https://hdl.handle.net/10356/169492 https://www.mdpi.com/2075-4418/13/10/1711 |
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1814047299360260096 |