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Published in: World Journal of Pediatrics 1/2020

01-02-2020 | Glucocorticoid | Original Article

Analysis of clinical manifestations and treatment in 26 children with fibrodysplasia ossificans progressiva in China

Authors: Jun-Mei Zhang, Cai-Feng Li, Shuang-Ying Ke, Yu-Rong Piao, Tong-Xin Han, Wei-Ying Kuang, Jiang Wang, Jiang-Hong Deng, Xiao-Hua Tan, Chao Li

Published in: World Journal of Pediatrics | Issue 1/2020

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Abstract

Background

Fibrodysplasia ossificans progressiva (FOP) is a rare and disabling heritable connective tissue disease that is difficult to treat. This study seeks to explore the clinical characteristics, clinical manifestations, treatment and prognosis of FOP to provide a clinical basis for its early diagnosis and treatment.

Methods

Twenty-six children with FOP were retrospectively analyzed in terms of their onset, clinical manifestations, auxiliary examinations and treatment.

Results

Among the 26 cases, the youngest age of manifestation of mass was 8 days after birth, and the average age was 3 years and 2 months. The peak age was 2–5 years old. Inflammatory mass and toe-finger deformity are the main early clinical manifestations of the disease. These inflammatory masses often lead to hard osteogenic deposits that initially mainly involve the central axis, such as the neck (22/26, 84.6%), back (20/26, 76.9%), and head (13/26, 50%). Toe-finger deformity mainly manifests as symmetrical great toe deformity, or short and deformed thumb and little finger. The diagnosis of FOP requires typical clinical manifestations or ACVR1 gene detection. The main therapeutic drugs for FOP include glucocorticoids and non-steroidal anti-inflammatory drugs. Although not compliant with the recommended medical management of FOP, in our clinical practice children with uncontrollable illness could be treated using a variety of immunosuppressive agents in combination.

Conclusions

FOP is a rare autosomal dominant heritable disease. The main clinical manifestations observed in this study were recurrent inflammatory mass and toe-finger deformity. If the diagnosis and treatment are not performed in a timely manner, serious complications are likely to affect the prognosis. Therefore, early diagnosis and active treatment should be performed.
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Metadata
Title
Analysis of clinical manifestations and treatment in 26 children with fibrodysplasia ossificans progressiva in China
Authors
Jun-Mei Zhang
Cai-Feng Li
Shuang-Ying Ke
Yu-Rong Piao
Tong-Xin Han
Wei-Ying Kuang
Jiang Wang
Jiang-Hong Deng
Xiao-Hua Tan
Chao Li
Publication date
01-02-2020
Publisher
Springer Singapore
Published in
World Journal of Pediatrics / Issue 1/2020
Print ISSN: 1708-8569
Electronic ISSN: 1867-0687
DOI
https://doi.org/10.1007/s12519-019-00302-x

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