腹腔镜治疗6厘米的囊性嗜铬细胞瘤：一个具有挑战性的病例。

Bouassida Mehdi, Samet Ahmed, Mseddi Mohamed Amine, Smaoui Walid, Slimèn Mourad Hadj, Mhiri Mohamed Nabil

Urology Department, Academic Hospital Habib Bourguiba. Sfax, Tunisia.

Urol Case Rep. 2019 Jul 26;26:100978. doi: 10.1016/j.eucr.2019.100978. eCollection 2019 Sep.

Cystic pheochromocytoma is a very rare entity.Preoperative diagnosis is difficult because clinical, biochemical and radiologic findings are usually not consistent with a pheochromocytoma.Open surgery is traditionally the gold standard to avoid cyst rupture.we present a case of a 6 cm cystic pheochromocytoma treated by laparoscopy.

囊性嗜铬细胞瘤是一种非常罕见的疾病。术前诊断困难，因为临床、生化和影像学表现通常与嗜铬细胞瘤不符。传统上，开放手术是避免囊肿破裂的金标准。我们报告一例通过腹腔镜治疗的6厘米囊性嗜铬细胞瘤病例。