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Two rare manifestations of primary hyperparathyroidism: paralysis and peptic ulcer bleeding

机译:原发性甲状旁腺功能亢进症的两种罕见表现:麻痹和消化性溃疡出血

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摘要

Primary hyperparathyroidism revealed by thoracic spine brown tumor and peptic ulcer bleeding is rare. We presented a case of 33-year-old male patient who was admitted with paraplegia. Thoracic spine magnetic resonance imaging (MRI) showed extradural lesion at T4 level. He underwent surgical decompression in T4. According to histopathologic finding and elevated serum parathormone (PTH) and hypercalcemia (total serum calcium 12.1 mg/dL), the diagnosis of brown tumor was down. Ultrasonography of his neck showed a well-defined lesion of 26 × 14 × 6 mm. The day after surgery, he experienced 2 episodes of melena. Bedside upper gastrointestinal endoscopy showed gastric peptic ulcer with visible vessel. Treatment with intragastric local instillation of epinephrine and argon plasma coagulation was done to stop bleeding. After stabilization of the patient, parathyroidectomy was performed. Histologic study showed the parathyroid adenoma without any manifestation of malignancy. At discharge, serum calcium was normal (8.6 mg/dL). On 40th day of discharge, standing and walking status was normal.Learning points: class="unordered" style="list-style-type:disc">Thoracic spine involvement is a very rare presentation of primary hyperparathyroidism.The issue of whether primary hyperparathyroidism increases the risk of peptic ulcer disease remains controversial. However, gastrointestinal involvement has been reported in association with classic severe primary hyperparathyroidism.The treatment of brown tumor varies from case to case. class="head no_bottom_margin" id="__sec2title">BackgroundBrown tumor (also called ‘osteoclastoma’) is a benign lytic bone lesion due to primary or secondary hyperparathyroidism. Brown color of this tumor is due to the accumulation of osteoclast, blood and fibrous tissue (). It is found in up to 3% of hyperparathyroidism (). This tumor-like lesion may be presented as a solitary or multiple mass that involve bone and adjacent tissues. It rarely locates in the spine (). To our best knowledge, the case reports of thoracic spine brown tumor due to primary hyperparathyroidism were very rare. Spinal involvement by brown tumor occasionally causes acute neurological deterioration (). We present a case of paralysis due to brown tumor involving the thoracic spine in a patient with primary hyperparathyroidism.
机译:胸椎棕色肿瘤和消化性溃疡出血所揭示的原发性甲状旁腺功能亢进很少见。我们介绍了一例33岁男性患者,该患者被截瘫。胸椎磁共振成像(MRI)显示T4水平的硬膜外病变。他在T4接受了手术减压。根据组织病理学发现以及血清副甲状腺激素(PTH)升高和高钙血症(血清总钙12.1 mg / dL),诊断为棕色肿瘤。颈部超声检查显示病灶清晰,为26×14×6 mm。手术的第二天,他经历了两次黑斑病。床旁上消化道内镜检查可见胃消化性溃疡,血管可见。进行胃内局部滴注肾上腺素和氩气血浆凝结治疗以止血。患者稳定后,进行甲状旁腺切除术。组织学研究显示甲状旁腺腺瘤无任何恶性表现。出院时血钙正常(8.6μmg/ dL)。出院第40天,站立和行走状态正常。学习要点: class =“ unordered” style =“ list-style-type:disc”> <!-list-behavior = unordered prefix-word = mark- type = disc max-label-size = 0-> 胸椎受累是原发性甲状旁腺功能亢进症的一种非常罕见的表现。 原发性甲状旁腺功能亢进是否会增加消化性溃疡疾病的风险仍然存在争议。但是,据报道胃肠道受累伴有典型的严重原发性甲状旁腺功能亢进症。 棕色瘤的治疗因情况而异。 class =“ head no_bottom_margin” id =“ __ sec2title”>背景棕色肿瘤(也称为“破骨细胞瘤”)是由于原发性或继发性甲状旁腺功能亢进引起的良性溶解性骨病变。该肿瘤的褐色是由于破骨细胞,血液和纤维组织的积累所致。最多可发现3%的甲状旁腺功能亢进()。该肿瘤样病变可表现为累及骨和邻近组织的单个或多个肿块。它很少位于脊柱()中。据我们所知,由原发性甲状旁腺功能亢进引起的胸椎棕色肿瘤的病例报道非常罕见。棕色肿瘤累及脊髓有时会导致急性神经系统恶化()。我们在原发性甲状旁腺功能亢进症患者中出现一例因涉及胸椎的棕色肿瘤而麻痹的病例。

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