腹膜后副神经节瘤1例,表现为顽固性便秘伴麻痹性肠梗阻及高血糖加重

S. Hwang, Mikwang Kwon, S. Chon
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引用次数: 0

摘要

副神经节瘤是肾上腺外嗜铬细胞瘤,起源于特化的神经嵴细胞。它们分布在从上颈部到骨盆底的任何地方,并根据它们的解剖起源进行分类。功能性副神经节瘤可引起与嗜铬细胞瘤相同的临床表现,如高血压、糖尿病、肾上腺素能亢进症等。我们报告了一例66岁男性顽固性便秘患者的腹膜后副神经节瘤,其便秘是由麻痹性肠梗阻和未控制的高血糖引起的。确诊后,切除副神经节瘤,其临床症状及持续高血糖均成功消除
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A Case of Retroperitoneal Paraganglioma Manifested as Intractable Constipation with Paralytic Ileus and Aggravated Hyperglycemia
Paragangliomas are extra-adrenal pheochromocytomas that arise from specialized neural crest cells. They are distributed anywhere from the upper neck to the pelvic floor, a nd they are classified on the basis of their anatomic origin. Functioning paragangliomas can cause the same clinical manifestations as pheochromocytoma, such as hypertension, diabetes mellitus, hyperadrenergic spells and so on. We experienced a retroperitoneal paraganglioma that was found in 66 year-old male who suffered from intractable constipation, and his constipation was caused by paralytic ileus and uncontrolled hyperglycemia. After he was diagnosed, removal of the paraganglioma was done and his clinical symptoms and sustained hyperglycemia were successfully
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