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首页> 外文期刊>National Journal of Maxillofacial Surgery >Osteitis fibrosa cystica of mandible in hyperparathyroidism-jaw tumor syndrome: A rare presentation and review of literature
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Osteitis fibrosa cystica of mandible in hyperparathyroidism-jaw tumor syndrome: A rare presentation and review of literature

机译:甲状旁腺功能亢进-下颌肿瘤综合征下颌骨纤维性膀胱炎:一种罕见的表现和文献复习

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摘要

Brown's tumor, also referred as osteitis fibrosa cystica is a rare nonneoplastic diagnostically challenging consequence of hyperparathyroidism (HPT) which occurs due to increased parathormone secretions in blood, causing excessive calcium resorption from kidneys, bone resorption, and phosphaturia. Brown's tumor is a misnomer, presenting as cystic expansile lesions in bone, often misdiagnosed as neoplastic lesion or granuloma or abscess in bones. It can affect long bones, clavicle, ribs, and pelvis. According to literature, skeletal manifestations of Brown tumor is relatively rare and occurs in <2% of the cases of HPT. We present a case of a female 15-year-old patient who presented with bleeding gums and an expansile lesion in mandible whose previous investigations elsewhere suggested a malignant lesion. However, further investigations revealed it to be Brown's tumor with primary HPT which is a rare genetic disorder, known as HPT-Jaw Tumor Syndrome (HPT-JT).
机译:布朗氏肿瘤(也称为纤维囊性囊炎)是甲状旁腺功能亢进症(HPT)罕见的非肿瘤诊断挑战性结果,其发生原因是血液中副甲状腺激素分泌增加,导致肾脏中钙的过度吸收,骨吸收和血尿。布朗氏肿瘤是一种误称,表现为骨骼中的囊性扩张性病变,通常被误诊为骨骼中的肿瘤性病变或肉芽肿或脓肿。它会影响长骨,锁骨,肋骨和骨盆。根据文献,布朗肿瘤的骨骼表现相对罕见,发生在HPT病例的2%以下。我们提供了一个女性15岁患者的案例,该患者出现牙龈出血和下颌骨扩张性病变,其先前在其他地方的研究表明存在恶性病变。但是,进一步的研究表明,它是原发性HPT的布朗氏肿瘤,这是一种罕见的遗传疾病,称为HPT-Jaw肿瘤综合征(HPT-JT)。

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