Skeletal fluorosis secondary to methoxyflurane use for chronic pain

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM
JBMR Plus Pub Date : 2024-03-07 DOI:10.1093/jbmrpl/ziae032
Yeung-Ae Park, Walter E Plehwe, Kapilan Varatharajah, Sophie Hale, Michael Christie, Christopher J Yates
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Abstract

Skeletal fluorosis is rare and occurs secondary to chronic high amounts of fluoride consumption, manifesting as diffuse osteosclerosis, skeletal pain, connective tissue calcification, and increased fracture risk. Methoxyflurane is a volatile fluorinated hydrocarbon inhaled analgesic, and the maximum recommended dose is 15 mL (99.9 % w/w) per week. A rodent study found increased skeletal fluoride after methoxyflurane exposure. However, skeletal fluorosis secondary to methoxyflurane use in humans has rarely been reported. We present the case of a 47-year-old female with diffuse osteosclerosis secondary to fluorosis from methoxyflurane use for chronic pain presenting with three years of generalized bony pain and multiple fragility fractures. Lumbar spine bone mineral density was elevated. CT and radiographs demonstrated new-onset marked diffuse osteosclerosis, with calcification of interosseous membranes and ligaments and a bone scan demonstrated grossly increased uptake throughout the skeleton. Biochemistry revealed an elevated alkaline phosphatase and bone turnover markers, mild secondary hyperparathyroidism with vitamin D deficiency and mild renal impairment. Zoledronic acid, prescribed for presumed Paget’s disease, severely exacerbated bony pain. Urinary fluoride was elevated (7.3 mg/L; reference range <3.0 mg/L) and the patient revealed using methoxyflurane 9 mL per week for eight years for chronic pain. A decalcified bone biopsy revealed haphazardly arranged cement lines and osteocytes lacunae and canaliculi, consistent with an osteosclerotic process. Focal subtle basophilic stippling around osteocyte lacunae was suggestive of fluorosis. Although fluorosis is not a histological diagnosis, the presence of compatible histology features was supportive of the diagnosis in this case with clinical-radiological-pathological correlation. Skeletal fluorosis should be considered as a cause of acquired diffuse osteosclerosis. Methoxyflurane should not be recommended for chronic pain. The risk of repeated low-dose exposure to fluoride from methoxyflurane use as analgesia may be greater than expected, and the maximum recommended dose for methoxyflurane may require re-evaluation to minimize skeletal complications.
因使用甲氧氟醚治疗慢性疼痛而继发的骨骼氟中毒
骨骼氟中毒十分罕见,是由于长期大量摄入氟而继发的,表现为弥漫性骨硬化、骨骼疼痛、结缔组织钙化和骨折风险增加。甲氧氟醚是一种挥发性含氟碳氢化合物吸入镇痛剂,建议的最大剂量为每周 15 毫升(99.9% w/w)。一项啮齿动物研究发现,接触甲氧氟烷后骨骼氟化物增加。然而,人类因使用甲氧氟烷而继发骨骼氟中毒的报道却很少见。我们介绍了一例因使用甲氧氟烷治疗慢性疼痛而继发氟中毒的弥漫性骨硬化症患者,该患者 47 岁,三年来出现全身骨痛和多处脆性骨折。腰椎骨矿物质密度升高。CT和X光片显示新近出现明显的弥漫性骨硬化,骨间膜和韧带钙化,骨扫描显示整个骨骼的摄取量明显增加。生化检查显示碱性磷酸酶和骨转换标志物升高,继发性甲状旁腺功能亢进伴维生素 D 缺乏,肾功能轻度受损。唑来膦酸是治疗假定的帕吉特氏病的处方药,它严重加剧了骨痛。尿氟升高(7.3 毫克/升;参考值范围小于 3.0 毫克/升),患者透露因慢性疼痛每周使用 9 毫升甲氧氟烷,已持续八年。脱钙骨活检显示,骨水泥线和骨细胞裂隙及管状突起杂乱排列,与骨硬化过程一致。骨细胞裂隙周围的局部细微嗜碱性斑纹提示为氟中毒。虽然氟中毒不是一种组织学诊断,但该病例的组织学特征与临床、放射学和病理学的相关性支持了这一诊断。骨骼氟中毒应被视为获得性弥漫性骨硬化症的病因之一。慢性疼痛患者不宜使用甲氧氟醚。使用甲氧氟烷镇痛时反复低剂量接触氟化物的风险可能比预期的要大,因此可能需要重新评估甲氧氟烷的最大推荐剂量,以尽量减少骨骼并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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