X-linked Rickets with Inflammatory Sacroiliitis-like Presentation: A Case Report and Literature Review

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Abstract

Background: Hypophosphatemic rickets can cause a variety of bone and joint symptoms, one of its rare presentations is sacroiliac joint involvement, which may be mistaken for inflammatory spondylitis. Discussion: Here, we report the case of a 31-year-old African American woman who presented with a 2-year history of lower back pain and morning stiffness initially suspected to be due to inflammatory spondyloarthritis. Laboratory tests revealed negative inflammatory markers, normal serum calcium, vitamin D3, and parathyroid hormone level: - However, alkaline phosphatase levels were elevated and serum phosphorus level was low. MRI of the lumbosacral spine revealed mild widening of the sacroiliac joint with periarticular sclerosis. Her condition was attributed to a known diagnosis of X-linked hypophosphatemic rickets affecting her sacroiliac joints. Her symptoms gradually improved after conservative treatment with physical therapy, NSAIDs, phosphate and vitamin D supplementations. Based on our literature review, we have come across only five rickets cases with similar presentations. Two paints previously undiagnosed hypophosphatemic rickets at 14 and 35 years, respectively. One case was related to vitamin D-deficient rickets, and the final two cases were adult-onset vitamin D-resistant rickets misdiagnosed as ankylosing spondylitis. Radiological signs of sacroiliac joint involvement in these cases include narrowing of the sacroiliac joints, fusion of the sacroiliac joints, subchondral hypointense signal changes, and chondral surface irregularities. Conclusion: Vitamin D supplementation significantly reduce the incidence of rickets; however, there are still cases of familial rickets that can present with a variety of symptoms, including signs and symptoms consistent with inflammatory spondylitis, which can be easily misdiagnosed or mistreated if this presentation is not recognized.
x连锁佝偻病伴炎性骶髂炎样表现:1例报告及文献回顾
背景:低磷血症佝偻病可引起多种骨和关节症状,其罕见的表现之一是骶髂关节受累,这可能被误认为是炎症性脊柱炎。讨论:在这里,我们报告一个31岁的非裔美国女性,她提出了2年的腰痛和晨僵病史,最初怀疑是由于炎症性脊柱炎。实验室检查显示炎症标志物阴性,血清钙、维生素D3和甲状旁腺激素水平正常:-然而,碱性磷酸酶水平升高,血清磷水平低。腰骶棘MRI显示骶髂关节轻度增宽伴关节周围硬化。她的病情是由于已知的x连锁低磷佝偻病影响她的骶髂关节。经物理治疗、非甾体抗炎药、补充磷酸盐及维生素D等保守治疗后症状逐渐好转。根据我们的文献综述,我们只遇到了5例类似的佝偻病病例。两名患者分别在14岁和35岁时患有先前未确诊的低磷血症佝偻病。1例与维生素d缺乏性佝偻病有关,最后2例为成人发病的维生素d抗性佝偻病,误诊为强直性脊柱炎。这些病例的骶髂关节受累的影像学征象包括骶髂关节狭窄、骶髂关节融合、软骨下低信号改变和软骨表面不规则。结论:补充维生素D可显著降低佝偻病的发病率;然而,仍然有一些家族性佝偻病的病例可以表现出各种各样的症状,包括与炎症性脊柱炎一致的体征和症状,如果这种表现不被识别,很容易被误诊或误治。
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