Brown tumor of the mandible - a possible clinical manifestation of primary hyperparathyreoidism

IF 0.2 4区 医学 Q4 MEDICINE, GENERAL & INTERNAL Vojnosanitetski pregled Pub Date : 2023-01-01 DOI:10.2298/vsp220809004m
Andrijana Milankov, M. Mitrović, T. Icin, B. Bajkin, Vukadin Milankov
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Abstract

Introduction. One of possible manifestations of primary hyperparathyroidism (PHPT) is the appearance of a benign bone tumor. We hereby present a case of a young woman whose first clinical manifestation of PHPT was a brown tumor of the mandible. Case report. A female patient was hospitalized in the Clinic of Endocrinology, Diabetes and Metabolic Disease due to the problems occurring in the form of nausea, exhaustion, feeling of suffocation, dysphagia, pain in the right ear and the right half of the cheeks, who was under suspicion of primary hyperparathyroidism (PHPT). Initial laboratory findings pointed out the high levels of parathyroid hormone (PTH) and Ca2+ ions, low levels of vitamin D and increased parameters of bone metabolism with signs of osteopenia. Cone beam computed tomography (CBCT) revealed a presence of bilateral radiolucent lesions of the mandible. Scintigraphy showed a retrosternal hot focus consistent with parathyroid adenoma. Parathyroidectomy was performed with following normalization of PTH values, bone metabolism parameters, and normalization of the Ca2+ ion values. Four months after parathyroidectomy, there was a complete resolution of clinical and radiological findings of initial tumefaction of the mandible. Conclusion. Brown tumors are rare first clinical manifestation of PHPT. Because of their histological similarities with other giant-cell lesions (GCL), definitive diagnosis is sometimes difficult, and is based on correlation with radiological and laboratory findings. Due to spontaneous regression of bone lesions after treatment of the basic cause of PHPT, brown tumors should be considered in the differential diagnosis of any giant-cell tumor lesions in order to avoid unnecessary surgical procedure.
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下颌骨棕色肿瘤-原发性甲状旁腺功能亢进的一种可能临床表现
介绍。原发性甲状旁腺功能亢进(PHPT)的可能表现之一是出现良性骨肿瘤。我们在此提出一个病例的年轻女性,其PHPT的第一个临床表现是一个棕色肿瘤的下颌骨。病例报告。1例女性患者因出现恶心、乏力、窒息感、吞咽困难、右耳及右半颊疼痛等症状,怀疑为原发性甲状旁腺功能亢进(PHPT),在内分泌、糖尿病及代谢疾病门诊就诊。最初的实验室结果指出,甲状旁腺激素(PTH)和Ca2+离子水平高,维生素D水平低,骨代谢参数增加,伴有骨质减少的迹象。圆锥束计算机断层扫描(CBCT)显示双侧下颌骨的放射性病变。显像显示胸骨后热灶与甲状旁腺瘤一致。甲状旁腺切除术后,PTH值正常化,骨代谢参数和Ca2+离子值正常化。甲状旁腺切除术后4个月,有一个完全解决的临床和影像学表现,最初的下颌骨肿胀。结论。褐色肿瘤是PHPT罕见的首发临床表现。由于其与其他巨细胞病变(GCL)的组织学相似,明确的诊断有时是困难的,并基于放射学和实验室结果的相关性。由于PHPT的基本病因治疗后,骨病变会自发消退,因此在鉴别诊断巨细胞肿瘤病变时应考虑棕色肿瘤,以避免不必要的手术治疗。
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来源期刊
Vojnosanitetski pregled
Vojnosanitetski pregled MEDICINE, GENERAL & INTERNAL-
CiteScore
0.50
自引率
0.00%
发文量
161
审稿时长
3-8 weeks
期刊介绍: Vojnosanitetski pregled (VSP) is a leading medical journal of physicians and pharmacists of the Serbian Army. The Journal is published monthly.
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