Zouraq Sara Azzabi, Haloua Meryem, Alami Badr, Lamrani Moulay Youssef Alaoui, Maaroufi Mustapha, Boubbou Meryem
Service de Radiologie, CHU HASSAN II de Fès, Fez, Morocco.
Faculté de médecine et de pharmacie de Fès, USMBA, Fez, Morocco.
Radiol Case Rep. 2022 May 6;17(7):2342-2345. doi: 10.1016/j.radcr.2022.03.112. eCollection 2022 Jul.
Pheochromocytomas arising from outside the adrenal glands are called paragangliomas and constitute a rare disease and can occur in the pelvic retroperitoneum. Symptoms of excess catecholamine production, as well as elevated urine vanillylmandelic acid levels and serum and urine norepinephrine levels, are highly diagnostic for paraganglioma. Imaging can be helpful for the diagnostic of these pelvic tumors, differentiating them from other pelvic masses. We hereby present a case of pelvic malignant paraganglioma.
起源于肾上腺外的嗜铬细胞瘤称为副神经节瘤,是一种罕见疾病,可发生于盆腔腹膜后。儿茶酚胺分泌过多的症状,以及尿香草扁桃酸水平、血清和尿去甲肾上腺素水平升高,对副神经节瘤具有高度诊断价值。影像学检查有助于诊断这些盆腔肿瘤,并将它们与其他盆腔肿块区分开来。我们在此报告一例盆腔恶性副神经节瘤病例。