Avinoach I, Robinson C R, Avinoah E, Peiser J
Institute of Pathology, Soroka Medical Centre, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Histopathology. 1989 Aug;15(2):195-6. doi: 10.1111/j.1365-2559.1989.tb03067.x.
We report a case of an adrenal lipoma, a very rare lesion first described in 1899 and of which a total of six cases have previously been reported (Lange 1966, Page, De Lellis & Hough 1986). Five of these cases were found incidentally at post mortem. In one case an acute hypertensive episode intra-operatively simulated the signs of phaeochromocytoma and contributed directly to the patient's death (Lange 1966). Intra-operative hypertension also occurred in our patient.
我们报告一例肾上腺脂肪瘤，这是一种非常罕见的病变，于1899年首次被描述，此前总共报告过6例（兰格，1966年；佩奇、德莱利斯和霍夫，1986年）。其中5例是在尸检时偶然发现的。在1例中，术中急性高血压发作模拟了嗜铬细胞瘤的症状，直接导致了患者死亡（兰格，1966年）。我们的患者术中也出现了高血压。
