Park Yeung-Ae, Plehwe Walter E, Varatharajah Kapilan, Hale Sophie, Christie Michael, Yates Christopher J
Department of Diabetes & Endocrinology, Royal Melbourne Hospital, Melbourne, Victoria 3052, Australia.
The Epworth Centre, Richmond, Victoria 3121, Australia.
JBMR Plus. 2024 Mar 7;8(5):ziae032. doi: 10.1093/jbmrpl/ziae032. eCollection 2024 May.
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 wk. 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-yr-old female with diffuse osteosclerosis secondary to fluorosis from methoxyflurane use for chronic pain, presenting with 3 yr of generalized bony pain and multiple fragility fractures. Lumbar spine BMD was elevated. CT and radiographs demonstrated new-onset marked diffuse osteosclerosis, with calcification of interosseous membranes and ligaments, and a bone scan demonstrated a 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 wk for 8 yr for chronic pain. A decalcified bone biopsy revealed haphazardly arranged cement lines and osteocytes lacunae and canaliculi, which was 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.
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. We present the case of a 47-yr-old female with skeletal fluorosis secondary to long-term methoxyflurane for chronic pain. The risk of repeated low-dose exposure to fluoride from methoxyflurane use for analgesia may be greater than expected, and the maximum recommended dose for methoxyflurane may require re-evaluation to minimize skeletal complications.
骨氟中毒较为罕见,继发于长期大量摄入氟化物,表现为弥漫性骨硬化、骨骼疼痛、结缔组织钙化以及骨折风险增加。甲氧氟烷是一种挥发性含氟烃类吸入性镇痛药,最大推荐剂量为每周15毫升(99.9%重量/重量)。一项啮齿动物研究发现,接触甲氧氟烷后骨骼中的氟含量增加。然而,人类使用甲氧氟烷继发骨氟中毒的情况鲜有报道。我们报告一例47岁女性病例,因使用甲氧氟烷治疗慢性疼痛继发氟中毒,出现弥漫性骨硬化,伴有3年的全身性骨痛和多处脆性骨折。腰椎骨密度升高。CT和X线片显示新发明显弥漫性骨硬化,骨间膜和韧带钙化,骨扫描显示全身摄取明显增加。生化检查显示碱性磷酸酶和骨转换标志物升高,伴有维生素D缺乏的轻度继发性甲状旁腺功能亢进以及轻度肾功能损害。因疑似佩吉特病而开具的唑来膦酸严重加剧了骨痛。尿氟升高(7.3毫克/升;参考范围<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,持续8年。脱钙骨活检显示骨水泥线、骨细胞陷窝和小管排列紊乱,符合骨硬化过程。骨细胞陷窝周围局灶性细微嗜碱性点彩提示氟中毒。虽然氟中毒不是组织学诊断,但在该病例中,具有相符的组织学特征并结合临床-放射-病理相关性支持了诊断。骨氟中毒应被视为获得性弥漫性骨硬化的一个病因。不建议将甲氧氟烷用于慢性疼痛。反复低剂量接触甲氧氟烷用作镇痛剂所产生的氟化物风险可能比预期的更大,甲氧氟烷的最大推荐剂量可能需要重新评估,以尽量减少骨骼并发症。
骨氟中毒较为罕见,继发于长期大量摄入氟化物,表现为弥漫性骨硬化、骨骼疼痛、结缔组织钙化以及骨折风险增加。我们报告一例47岁女性病例,因长期使用甲氧氟烷治疗慢性疼痛继发骨氟中毒。反复低剂量接触甲氧氟烷用作镇痛剂所产生的氟化物风险可能比预期的更大,甲氧氟烷的最大推荐剂量可能需要重新评估,以尽量减少骨骼并发症。