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青春期晚期多发棕色瘤酷似骨转移:一例具有挑战性的病例报告。

Multiple brown tumor in late adolescence mimicking bone metastasis: A challenging case report.

作者信息

Paramita Ratri Dinar, Rahardjo Paulus

机构信息

Department of Radiology, Dr. Soetomo General Academic Hospital, Surabaya.

Department of Radiology, Faculty of Medicine - Universitas Airlangga, Surabaya.

出版信息

Radiol Case Rep. 2024 Jul 24;19(10):4266-4272. doi: 10.1016/j.radcr.2024.07.008. eCollection 2024 Oct.

Abstract

Brown tumors, resulting from elevated osteoclast activity, are uncommon skeletal symptoms of hyperparathyroidism. Because of their similar characteristics, it is challenging to differentiate these tumors from multiple myeloma or osteolytic metastases. A 24-year-old female with a painful lump in her left thigh and arm in the past 10 months. The patient reported a history of left femoral bone fracture over a year ago due to low-impact trauma. Plain radiograph images and chest MSCT showed osteolytic lesions at the skull, ribs, and extremities, followed by increased Tc99 bone scan image uptake. Thyroid ultrasound and cervical MSCT showed parathyroid mass. Biochemical and pathologic examination supported the diagnosis of brown tumor. A multidisciplinary approach, including clinical evaluation, biochemical assessment, pathological examination, and advanced imaging modalities such as CT scan, MRI, and bone scintigraphy, is necessary for the differential diagnosis of brown tumors from bone metastasis. Medical history, PTH, calcium levels in the blood, and additional systemic symptoms can all be used to help distinguish between the 2 disorders. The clinical presentation and imaging findings of brown tumors may mimic bone metastasis, necessitating comprehensive evaluation. Multidisciplinary collaboration plays a vital role in reaching an accurate diagnosis. Increased awareness of brown tumors as a potential mimic of bone metastasis may help prevent misdiagnosis and ensure optimal care for patients presenting with osteolytic bone lesions associated with hyperparathyroidism.

摘要

棕色瘤是由破骨细胞活性升高引起的,是甲状旁腺功能亢进症罕见的骨骼症状。由于其相似的特征,将这些肿瘤与多发性骨髓瘤或溶骨性转移瘤区分开来具有挑战性。一名24岁女性在过去10个月中左大腿和手臂出现疼痛性肿块。患者报告一年多前因低冲击力创伤导致左股骨骨折。X线平片和胸部MSCT显示颅骨、肋骨和四肢有溶骨性病变,随后Tc99骨扫描图像摄取增加。甲状腺超声和颈部MSCT显示甲状旁腺肿块。生化和病理检查支持棕色瘤的诊断。多学科方法,包括临床评估、生化评估、病理检查以及CT扫描、MRI和骨闪烁显像等先进成像方式,对于棕色瘤与骨转移的鉴别诊断是必要的。病史、甲状旁腺激素、血液中的钙水平以及其他全身症状都可用于帮助区分这两种疾病。棕色瘤的临床表现和影像学表现可能与骨转移相似,需要进行全面评估。多学科协作在做出准确诊断方面起着至关重要的作用。提高对棕色瘤可能模拟骨转移的认识,可能有助于防止误诊,并确保为患有与甲状旁腺功能亢进相关的溶骨性骨病变的患者提供最佳治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7612/11318562/e323735bd405/gr1.jpg

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