Sano Futoshi, Fujikawa Naoya, Hirai Kotaro, Ueki Teiichiro, Kitami Kazuo
Department of Urology, Fujisawa City Hospital.
Hinyokika Kiyo. 2006 Jan;52(1):15-7.
The presentation of pheochromocytoma is quite variable. We report a case of previously undiscovered pheochromocytoma which was manifested by traumatic retroperitoneal hemorrhage. A 79-year-old man fell from his bicycle and was admitted to the emergency room complaining of right flank pain. Enhanced computed tomography (CT) revealed hemorrhage around the right adrenal gland. Since the plasma catecholamine levels were elevated, we suspected the presence of pheochromocytoma. After absorption of the hematoma, the tumor appeared clearly. The diagnosis of pheochromocytoma was confirmed through urine catecholamine testing and 131I-MIBG scintigraphy. Six months after the injury, the tumor was surgically resected. Traumatic hemorrhage of pheochromocytoma is extremely rare; only 3 cases have been reported in the literature.
嗜铬细胞瘤的临床表现差异很大。我们报告一例此前未被发现的嗜铬细胞瘤,其表现为创伤性腹膜后出血。一名79岁男性从自行车上摔倒,因右侧胁腹疼痛被送入急诊室。增强计算机断层扫描(CT)显示右肾上腺周围出血。由于血浆儿茶酚胺水平升高,我们怀疑存在嗜铬细胞瘤。血肿吸收后,肿瘤清晰显现。通过尿儿茶酚胺检测和131I-间碘苄胍闪烁扫描术确诊为嗜铬细胞瘤。受伤6个月后,肿瘤被手术切除。嗜铬细胞瘤创伤性出血极为罕见;文献中仅报道过3例。