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Urinary bladder malignant paraganglioma with vertebral metastasis: a case report with literature review

机译:伴有椎骨转移的膀胱恶性副神经节瘤1例并文献复习

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摘要

Paraganglioma is a rare neuroendocrine neoplasm observed in patients of all ages, with an estimated incidence of 3/1,000,000 population. It has long been recognized that some cases are familial. The majority of these tumors are benign, and the only absolute criterion for malignancy is the presence of metastases at sites where chromaffin tissue is not usually found. Some tumors show gross local invasion and recurrence, which may indeed kill the patient, but this does not necessarily associate with metastatic potential. Here, we report a case of vertebral metastatic paraganglioma that occurred 19 months after the patient had undergone partial cystectomy for urinary bladder paraganglioma. We believe this to be a rarely reported bone metastasis of paraganglioma arising originally within the urinary bladder. In this report, we also provide a summary of the general characteristics of this disease, together with progress in diagnosis, treatment, and prognosis.
机译:副神经节瘤是在所有年龄段的患者中观察到的罕见神经内分泌肿瘤,估计发病率为3 / 1,000,000人口。长期以来,人们已经认识到有些病例是家族性的。这些肿瘤大多数是良性的,并且唯一确定恶性肿瘤的标准是在通常不存在嗜铬组织的部位存在转移。一些肿瘤显示出明显的局部浸润和复发,可能确实杀死了患者,但这不一定与转移潜能有关。在这里,我们报告了一个椎管转移性副神经节瘤病例,该病例在患者因膀胱副神经节瘤进行了部分膀胱切除术后19个月发生。我们认为这是最初在膀胱内发生的副神经节瘤的骨转移很少报道。在本报告中,我们还概述了该疾病的一般特征,以及在诊断,治疗和预后方面的进展。

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