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首页> 外文期刊>American journal of otolaryngology >Brown tumors of the jaws associated with primary or secondary hyperparathyroidism. A clinical study and review of the literature.
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Brown tumors of the jaws associated with primary or secondary hyperparathyroidism. A clinical study and review of the literature.

机译:与原发性或继发性甲状旁腺功能亢进有关的颌骨褐色瘤。临床研究和文献综述。

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摘要

PURPOSE: The aim of this article is to present the development of brown tumors in the jaws as a definite feature of hyperparathyroidism (HPT), whether primary or secondary. PATIENTS AND METHODS: The study included 2 cases of primary HPT and 3 cases of secondary HPT associated with brown tumors in the jaws. The patients presented in our clinic at the "G. Papanikolaou" Hospital in Thessaloniki for treatment of their disease. The patients were 4 women and 1 man, and patient's ages ranged from 21 to 76 years. Four cases of the brown tumors involved the mandible, and 1 case involved the maxilla and the maxillary sinus. The surgical excision of bone lesions and treatment of primary or secondary HPT were performed on the patients in our study. RESULTS: Patient 1 (primary HPT, caused by an adenoma of the right parathyroid glands) was treated with surgical removal of the maxillary lesion and excision of the adenoma. Three years later, the patient is free of the disease, with no recurrence of the brown tumor. Patient 2 (primary HPT, caused by an adenoma of the right parathyroid glands) was treated with excision of the adenoma. One year later, a second bone lesion developed in the mandible, and 3(1/2) of the fourth parathyroid (right) glands was removed. The patient is being observed. The other 3 patients with brown tumors associated with secondary HPT were treated with excision of the bone lesions; HPT was treated with hemodialysis (2 patients) and renal transplantation (1 patient). For the patients treated with hemodialysis, the disease is under control and there is no recurrence of the brown tumors. The patient who underwent transplantation is free of the disease 7 years later. CONCLUSIONS: Primary or secondary HPT may be recognized by the presence of an osteolytic lesion with giant cells, a condition referred as "brown tumor." The most useful therapy for patients with brown tumors is surgical excision of bone lesions and therapy (surgical or medical) for primary or secondary HPT.
机译:目的:本文的目的是介绍颌骨棕色肿瘤的发展,作为原发性或继发性甲状旁腺功能亢进症(HPT)的明确特征。患者与方法:该研究包括2例原发性HPT和3例继发性HPT与颌骨褐色肿瘤相关。这些患者在塞萨洛尼基的“ G. Papanikolaou”医院就诊,以治疗他们的疾病。患者为4名女性和1名男性,患者年龄为21至76岁。褐色肿瘤累及下颌4例,上颌骨及上颌窦1例。在本研究中,对患者进行了骨病变的手术切除以及原发性或继发性HPT的治疗。结果:患者1(原发性HPT,由右甲状旁腺腺瘤引起)接受了手术切除上颌病变并切除腺瘤的治疗。三年后,患者无疾病,褐色肿瘤未复发。患者2(原发性HPT,由右甲状旁腺腺瘤引起)经切除腺瘤治疗。一年后,下颌骨出现第二个骨病变,第四甲状旁腺(右)的3(1/2)个被切除。正在观察患者。其余3例伴有继发性HPT的褐色肿瘤患者,均经切除骨病变治疗。 HPT接受血液透析治疗(2例)和肾移植(1例)。对于接受血液透析治疗的患者,疾病得到了控制,褐色肿瘤没有复发。接受移植的患者在7年后没有疾病。结论:原发性或继发性HPT可通过存在巨细胞的溶骨性病变来识别,这种情况称为“棕色肿瘤”。对于患有褐色肿瘤的患者,最有用的治疗方法是手术切除骨病变以及对原发性或继发性HPT进行治疗(外科或医学)。

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