A 48-Year-Old Man With a Hip Fracture and Skin Rash: A Case Report

J. Anthony Parker MD , Runhua Hou MD
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Abstract

Background/Objective

Patients with systemic mastocytosis are at high risk of developing osteoporosis and fractures. Herein, we report a case of hip fragility fracture in a patient with indolent systemic mastocytosis and normal bone density.

Case Report

A 48-year-old man experienced a left femoral neck fracture after a fall. After a dose of oxycodone/hydromorphone postoperatively, he developed an anaphylactic reaction. Previously, he experienced a few other episodes of flushing, dizziness, and syncope precipitated by stress and alcohol. His examination was notable for pink and brown macules on his chest, back, arms, and legs. His laboratory test revealed a markedly elevated tryptase level of 171 ng/mL (<11 ng/mL). Treatment including cetirizine, montelukast, and ranitidine controlled his symptoms. His bone density test result was normal. Ten months after hip surgery, his c-terminal telopeptide of collagen type 1 and bone-specific alkaline phosphatase levels significantly increased. The bone scan demonstrated diffusely increased radiotracer uptake throughout the osseous structures. Given high bone turnover and the prior hip fracture, he received zoledronic acid yearly for 3 years, and no further fractures have occurred.

Discussion

The case is unusual as the fracture occurred despite normal bone density and significant osteosclerosis, which was previously considered protective against fractures. Additionally, rather than the spine, the fracture occurred in the hip, which is an uncommon site for mastocytosis-induced fractures.

Conclusion

Mastocytosis is a rare cause of osteoporosis, and it is important to keep this condition in the differential diagnosis of osteoporosis, particularly when the fracture presentation is atypical.

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一名髋部骨折并伴有皮疹的 48 岁男子:病例报告
背景/目的全身性肥大细胞增多症患者是骨质疏松症和骨折的高危人群。在此,我们报告了一例髋关节脆性骨折病例,患者患有懒惰型系统性肥大细胞增多症,骨密度正常。病例报告一名 48 岁的男子在一次跌倒后发生左股骨颈骨折。术后服用了一剂羟考酮/氢吗啡酮后,他出现了过敏反应。在此之前,他曾因压力和酒精而出现过几次潮红、头晕和晕厥。检查结果显示,他的胸部、背部、手臂和腿部出现粉红色和棕色斑丘疹。化验结果显示,他的胰蛋白酶水平明显升高,达到 171 纳克/毫升(11 纳克/毫升)。包括西替利嗪、孟鲁司特和雷尼替丁在内的治疗控制了他的症状。他的骨密度检测结果正常。髋关节手术后十个月,他的1型胶原蛋白c端端肽和骨特异性碱性磷酸酶水平明显升高。骨扫描显示,整个骨结构的放射性示踪剂摄取弥漫性增加。鉴于骨转换率高和之前的髋部骨折,他每年接受唑来膦酸治疗,持续了 3 年,没有再发生骨折。讨论该病例不同寻常,因为尽管骨密度正常且骨硬化明显,但还是发生了骨折,而骨硬化以前被认为对骨折具有保护作用。此外,骨折发生在髋部而非脊柱,这在肥大细胞增多症引起的骨折中并不常见。结论肥大细胞增多症是骨质疏松症的罕见病因,因此在骨质疏松症的鉴别诊断中保留这一病症非常重要,尤其是当骨折表现不典型时。
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来源期刊
AACE Clinical Case Reports
AACE Clinical Case Reports Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.30
自引率
0.00%
发文量
61
审稿时长
55 days
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