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Complete laparoscopic excision of a giant retroperitoneal paraganglioma

机译:巨大腹膜后副神经节瘤的完全腹腔镜切除

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摘要

Paragangliomas (or ‘extra-adrenal phaeochromocytomas’) are rare tumours arising from neural crest cells. They occur most commonly in the abdomen along the paraspinal sympathetic ganglion. The malignancy rate can be up to 35% and surgical resection is the recommended treatment. While laparoscopic excision of phaeochromocytomas is now well established, the overall number of cases of paragangliomas reported is much smaller owing to their rarity (even more so for giant paragangliomas of ≥8cm) and controversy remains over the completeness of excision. Furthermore, the risk of malignancy and recurrence rate are higher in paragangliomas, with incomplete excision giving rise to recurrent endocrinopathy and carcinomatosis. We report the case of a 26-year-old woman who underwent laparoscopic excision of an 8.2cm functioning paraganglioma. Complete resection of the tumour was achieved and the patient’s symptoms resolved. Twelve months later, she remains well with no evidence of recurrence.
机译:神经节旁瘤(或“肾上腺外嗜铬细胞瘤”)是神经rest细胞引起的罕见肿瘤。它们最常发生在椎旁交感神经节的腹部。恶性率可高达35%,建议手术切除。腹腔镜下对嗜铬细胞瘤的切除术已经很成熟,但由于其稀有性,报告的副神经节瘤病例总数要少得多(对于≥8cm的巨大副神经节瘤病例更是如此),并且在切除术的完整性方面仍存在争议。此外,副神经节瘤中恶性肿瘤和复发率的风险更高,切除不完全会导致复发性内分泌病和癌变。我们报告了一例26岁的妇女,该妇女接受了8.2cm正常功能的副神经节瘤的腹腔镜切除。肿瘤已完全切除,患者的症状得到缓解。十二个月后,她仍然没有复发的迹象。

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