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骨佩吉特病:沙特阿拉伯存在这种病吗?

Paget disease of the bone: does it exist in Saudi Arabia?

作者信息

Alshaikh Omalkhaire M, Almanea Hadeel, Alzahrani Ali S

机构信息

Department of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

出版信息

Ann Saudi Med. 2011 May-Jun;31(3):305-10. doi: 10.4103/0256-4947.75588.

Abstract

Paget disease of the bone is a chronic disease characterized by accelerated bone turnover with abnormal repair leading to expansion, pain and deformities. The disease is common in the West, but little if any information is available on its existence in the Arab world, including Saudi Arabia. We present four cases of Saudi patients with Paget disease with variable presentations. The first case, a 63-year-old woman with a history of papillary thyroid cancer, presented with bone, shoulder and chest wall pain and foci of uptake in the ribs and skull that were thought to be metastases, indicating the possibility of diagnostic difficulty in a patient with history of malignancy. Bone biopsy confirmed the diagnosis of Paget disease. The second case was a 47-year-old asymptomatic woman with an elevated alkaline phosphatase of 427 U/L, a common presentation but at an unusual age. Plain x-rays and bone scan confirmed the diagnosis. The third case was a 43-year-old man who presented with hearing impairment and right knee osteoarthritis, unusual presentations at a young age leading to a delay in diagnosis. The fourth case was a 45-year-old man who presented with sacroiliac pain and normal biochemical values, including a normal alkaline phosphatase. Bone biopsy unexpectedly revealed features of Paget disease, which evolved over time into a classical form. A common feature in all except the first case was the relatively young age. Paget disease does exist in Saudi Arabia, and it should be considered in the differential diagnosis of similar cases.

摘要

骨佩吉特病是一种慢性疾病,其特征为骨转换加速并伴有异常修复,进而导致骨质膨胀、疼痛和畸形。该病在西方较为常见,但关于其在阿拉伯世界(包括沙特阿拉伯)的存在情况,即便有相关信息也极为稀少。我们报告了4例沙特佩吉特病患者,其临床表现各异。首例患者为一名63岁女性,有乳头状甲状腺癌病史,表现为骨痛、肩部和胸壁疼痛,肋骨和颅骨有摄取灶,最初被认为是转移灶,这表明有恶性肿瘤病史的患者可能存在诊断困难。骨活检确诊为佩吉特病。第二例是一名47岁无症状女性,碱性磷酸酶升高至427 U/L,这是常见表现,但年龄不常见。X线平片和骨扫描确诊。第三例是一名43岁男性,表现为听力障碍和右膝骨关节炎,这些不常见的表现导致诊断延迟,当时患者年龄较轻。第四例是一名45岁男性,表现为骶髂关节疼痛,生化指标正常,包括碱性磷酸酶正常。骨活检意外发现佩吉特病特征,随时间推移发展为典型形式。除首例患者外,其他所有病例的一个共同特征是年龄相对较轻。沙特阿拉伯确实存在佩吉特病,在类似病例的鉴别诊断中应考虑该病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0261/3119975/e946b112de30/ASM-31-305-g001.jpg

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