Year: 2024
Type: article
Study design: Case Report
Abstract: A 14-year-old boy was brought to the rheumatology clinic with a two-year history of pain in the bilateral hip. The hip pain emerged after walking and subsided upon taking a break. There had been no preceding trauma or fever or history of receiving glucocorticoids. Physical examination showed no limitation in hip range of motion. The patient had no low back pain. Laboratory tests revealed normal levels of erythrocyte sedimentation rate, C-reactive protein, interferon-γ release assay, and endocrine hormones. His HLA-B27 was negative. (A) Pelvic X-ray and (B and C) computed tomography revealed a focal area of collapse in the bilateral femoral head (arrow). (D) Magnetic resonance imaging showed rough articular surface, (E) bone marrow edema and synovitis, and (F) “double-line sign” (arrow). These findings indicated an avascular necrosis of the femoral head (ANFH). His parents and sister were in good health. Nevertheless, the peripheral blood samples were collected from the patient and his family members, and the patient's blood sample was analyzed via the whole-exome sequencing. (G) It identified a de novo COL2A1: 3508G>T, p.Gly1170Cys heterozygous mutation in the patient and this gene in the patient's pedigree of the family was tested wild type confirmed by Sanger sequencing. A diagnosis of Legg–Calvé–Perthes disease (LCPD) was made. LCPD is an idiopathic ANFH in preadolescent children. Pain is primarily localized in the hip, occasionally accompanied by leg and knee pain, and most of the patients show limited hip internal rotation.1 Its incidence ranges from 0.4 of 100,000 to 29.0 of 100,000 in children younger than 15 years old.1 The cause of LCPD remains unknown. Mutations in the type II collagen, which are encoded by the COL2A1 gene, are associated with type II collagenopathies, including LCPD and ANFH. A heterozygous mutation (c.1888G>A, p.Gly630Ser) in exon 29 of COL2A1 leading to LCPD and ANFH had been reported in a Chinese family.2 Our patient demonstrates a novel heterozygous mutation in the COL2A1 gene that causes LCPD. The patient received a conservative treatment regimen of diclofenac sodium for pain relief and a brace to reduce pressure on the hip. Consent was obtained directly from the patient and parents. T1WI, T1-weighted imaging; T2WI, T2-weighted imaging. Supported by the Shanghai Jiao Tong University School of Medicine Affiliated Sixth People's Hospital (grant ynhg202115). The data underlying this article are available in the article. Disclosure form Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Source: ACR Open Rheumatology
DOI: 10.1002/acr2.11762
Authors: Ran Cui, Xin‐Yu Song, Hong Zhang, Sheng‐Ming Dai
Language: English
Topic: Bone and Joint Diseases
Subfield: Orthopedics and Sports Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,230
OpenAlex ID: W4403566580