Takizawa H, Narisawa R, Asakura H
The Third Department of Internal Medicine, Niigata University School of Medicine, Japan.
Am J Med Sci. 1999 Jan;317(1):63-6. doi: 10.1097/00000441-199901000-00011.
The authors discuss a case of pheochromocytoma in a 20-year-old man referred for anemia due to gastrointestinal bleeding. Pheochromocytoma uncommonly presents with gastrointestinal bleeding, and a pathologic diagnosis is rarely made without resection of the tumor. Imaging studies demonstrated a mass on the left kidney with metastases to the liver, and high levels of catecholamines in plasma and urine were suggestive of pheochromocytoma. Endoscopic examination of the gastrointestinal tract demonstrated a mass in the proximal jejunum near the ligament of Treitz and a mass with central ulceration in the upper jejunum; biopsy confirmed the pathologic diagnosis of malignant pheochromocytoma with jejunal invasion and metastases to the liver. Gastrointestinal bleeding is one of the manifestations of pheochromocytoma. This is the first case in which endoscopic biopsy determined a pathologic diagnosis of pheochromocytoma.
作者讨论了一例20岁男性嗜铬细胞瘤病例,该患者因胃肠道出血导致贫血前来就诊。嗜铬细胞瘤很少表现为胃肠道出血,若不切除肿瘤,很少能做出病理诊断。影像学检查显示左肾有一肿块并伴有肝转移,血浆和尿液中儿茶酚胺水平升高提示嗜铬细胞瘤。胃肠道内镜检查显示在Treitz韧带附近的空肠近端有一肿块,在上段空肠有一中央溃疡的肿块;活检证实为恶性嗜铬细胞瘤伴空肠侵犯和肝转移的病理诊断。胃肠道出血是嗜铬细胞瘤的表现之一。这是首例通过内镜活检确定嗜铬细胞瘤病理诊断的病例。