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首页> 外文期刊>Medicine. >Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report
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Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report

机译:原发性甲状旁腺功能亢进相关的多发面骨褐色瘤:临床病例报告

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摘要

Rationale: Only 4.5% of brown tumors involve facial bones; of these, solitary bone involvement is usual. Brown tumors of multiple facial bones are extremely rare. Here, we report the case of a brown tumor of multiple facial bones initially misdiagnosed as an odontogenic cyst. Patient concerns: A pregnant 26-year-old woman was referred to our hospital with painful swelling of multiple facial bones, anemia, urinary calculi, marasmus, and a history of multiple bone fractures. Laboratory examination revealed an elevated serum calcium level of 3.09 mmol/L (normal range: 2.0–2.8 mmol/L) and a low phosphorus level of 0.62 mmol/L (normal range: 0.81–1.65 mmol/L). The serum alkaline phosphatase concentration was 397 IU/L (normal range: 24–82 IU/L) and parathyroid hormone level was 267 pg/mL (normal range: 14–72 pg/mL). Cone beam computed tomography revealed multiple ossifying fibromas of the maxilla and mandible. Incisional biopsy revealed abundant spindle cells with areas of hemorrhage and haphazardly arranged diffuse multinucleated giant cells. Diagnoses: The patient was diagnosed with primary hyperparathyroidism (HPT). Interventions: She was treated by parathyroidectomy. Outcomes: The multiple osteitis fibrosa cystica gradually resolved as bone re-mineralized. The patient has been followed up for 2 years without evidence of tumor recurrence. Lessons: As multiple osteolytic lesions of facial bones can be caused by primary HPT, serum calcium and parathyroid hormone assays should be performed routinely when investigating these lesions.
机译:理由:只有4.5%的棕色肿瘤累及面骨;其中,孤立骨受累很常见。多个面部骨骼的褐色肿瘤极为罕见。在这里,我们报道了最初被误诊为牙源性囊肿的多个面部骨骼的棕色肿瘤。患者担忧:一名26岁的孕妇因多面部骨头肿胀,贫血,尿路结石,马拉斯莫斯病和多处骨折史而被转诊到我们医院。实验室检查发现血清钙水平升高了3.09 mmol / L(正常范围:2.0–2.8 mmol / L),磷水平低了0.62 mmol / L(正常范围:0.81–1.65 mmol / L)。血清碱性磷酸酶浓度为397 IU / L(正常范围:24-82 IU / L),甲状旁腺激素水平为267 pg / mL(正常范围:14-72 pg / mL)。锥形束计算机断层扫描显示上颌骨和下颌骨有多个骨化性纤维瘤。切开活检显示纺锤体细胞丰富,有出血区域,并随意分布弥散的多核巨细胞。诊断:该患者被诊断为原发性甲状旁腺功能亢进症(HPT)。干预措施:她接受了甲状旁腺切除术治疗。结果:随着骨骼再矿化,多囊性纤维囊性骨炎逐渐解决。对该患者进行了2年的随访,没有肿瘤复发的迹象。经验教训:由于原发性HPT可能引起面部骨骼的多种溶骨性病变,因此在调查这些病变时应常规进行血清钙和甲状旁腺激素测定。

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