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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Malignant Paraganglioma (Pheochromocytoma) of the Urinary Bladder: Report of a Case and Review of the Literature
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Malignant Paraganglioma (Pheochromocytoma) of the Urinary Bladder: Report of a Case and Review of the Literature

机译:膀胱的恶性副神经节瘤(嗜铬细胞瘤):一例报告并文献复习

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摘要

A rare case of malignant paraganglioma of the urinary bladder with metastasis to a lymph node in a 12-year-old girl is reported, and eight other previously recorded cases are reviewed. Headache, fainting, and hypertention initiated by voiding were the most prominent clinical symptoms. Hematuria was Present in three cases and aided cystoscopy were most diagnostic. Cystography, pelvic angiogtaphy, and cystoscopy were most diagnostic. Segmental cystectomy, when feasible. was the preferred surgical treatment. The prognosis was slightly better than for other forms of extraadrenal pheochromocytomas.
机译:据报道,在一个12岁女孩中,罕见的膀胱恶性副神经节瘤转移至淋巴结转移,并回顾了其他八例先前记录的病例。排尿引起的头痛,昏厥和高血压是最突出的临床症状。 3例存在血尿,辅助膀胱镜检查最能诊断。膀胱造影,骨盆血管造影和膀胱镜检查最能诊断。可行时行节段性膀胱切除术。是首选的手术治疗方法。预后比其他形式的肾上腺嗜铬细胞瘤好一些。

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