手术及病理均证实为左卵巢肾上腺样瘤。
目的：探讨肾上腺髓样脂肪瘤的临床、影像学及病理特点。
Objective: To investigate the clinical characteristics, imaging and pathological features of adrenal myelolipoma.
大鼠肾上腺嗜铬细胞瘤细胞PC12具有神经元样分化的潜能，在PC12细胞中转染并过量表达NECL2能够诱导细胞发生神经元样分化。
NECL2 distributed in cell body and protuberance of primary culture neuron. The rat adrenal gland tumor cell line PC12 can be induced into neuronal differentiation.
结论肾上腺髓样脂肪瘤的CT、MRI表现较具特征性，一般可在术前作出诊断。
Conclusion the ct and MRI manifestations of adrenal myelolipoma were characteristic features and the diagnosis can be reached before operation.
结论CT对肾上腺髓样脂肪瘤具有重要的诊断价值，可以首选检查方法。
Conclusion CT of adrenal myelolipoma has important diagnostic value, and can be the preferred screening method.
结果皮质腺瘤12例，皮质腺癌5例，嗜铬细胞瘤3例，髓样脂肪瘤4例，转移瘤6例，肾上腺节细胞神经瘤1例。
Results Of 31 cases, there were 12 adenomas, 5 adenocarcinomas, 3 pheochromocytomas, 4 myelolipomas, 6 metastatic tumor and 1 adrenal ganglioneuroma.
方法收集10例肾上腺髓样脂肪瘤的CT、MRI及临床、病理资料。
Methods Ten cases of adrenal myelolipoma were examined by CT and MRI.
方法收集10例肾上腺髓样脂肪瘤的CT、MRI及临床、病理资料。
Methods Ten cases of adrenal myelolipoma were examined by CT and MRI.
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