Yamakita N, Kikuchi M, Minamori Y, Goshima E, Murase H, Murayama M, Yasuda K, Miura K, Imaeda T, Sugiyama K
Nihon Naibunpi Gakkai Zasshi. 1985 Jun 20;61(6):677-89. doi: 10.1507/endocrine1927.61.6_677.
The image diagnoses of a case of so-called "nonfunctioning" adrenal adenoma, weak mineralocorticoids producing adrenal carcinoma, congenital adrenogenital syndrome due to 21-hydroxylase deficiency--simple virilizing form--, and 5 cases of pheochromocytoma were studied. In a patient with so-called "nonfunctioning" adrenal adenoma (2.3 X 3.0 X 3.3 cm), in which steroids biosynthesis was confirmed, computed tomography (CT) delineated the tumor shadow with extremely low density, and ultrasonography (US) demonstrated the round tumor echo with homogenous and low echogenicity at the superior region of the right renal pole. Adrenal scintigraphy also showed the tumor image. A weak mineralocorticoids-producing left adrenal carcinoma (3.5 X 3.5 X 3.0 cm) was shown as a heterogenous round tumor at the left lateral portion of the vertebra by CT. On adrenal scintigraphy under dexamethasone pretreatment, there was good uptake in the tumor and disappearance of the contralateral. Both bilateral adrenal images on CT in a patient with congenital adrenogenital syndrome were linear-shaped and markedly enlarged. The enlarged right adrenal was clearly demonstrated by US with an electronic sector scanner but not with an electronic linear scanner, although the left one was hardly shown by either US instruments. Three of 4 patients with pheochromocytomas examined by US were correctly detected, while in the remaining one the tumor image was judged to be a retroperitoneal tumor. CT also correctly demonstrated the former 3 pheochromocytomas, but misjudged the latter one as a pancreatic cancer. Good uptake of Adosterol by bilateral adrenals was shown in a case of extra-adrenal pheochromocytoma. Three of 4 cases of adrenal pheochromocytoma showed the isotope uptake of the contralateral normal adrenal alone. In another case of right adrenal pheochromocytoma, isotope accumulation in the colon obscured whether the isotope uptake in the right adrenal was shown or not.
对1例所谓“无功能”肾上腺腺瘤、1例分泌弱盐皮质激素的肾上腺皮质癌、1例因21-羟化酶缺乏所致先天性肾上腺皮质增生症(单纯男性化型)以及5例嗜铬细胞瘤的影像诊断进行了研究。在1例所谓“无功能”肾上腺腺瘤患者(肿瘤大小为2.3×3.0×3.3cm)中,已证实存在类固醇生物合成,计算机断层扫描(CT)显示肿瘤阴影密度极低,超声检查(US)显示右肾极上方区域有圆形肿瘤回声,回声均匀且低。肾上腺闪烁显像也显示了肿瘤影像。1例分泌弱盐皮质激素的左肾上腺皮质癌(3.5×3.5×3.0cm)在CT上表现为位于椎体左侧的不均匀圆形肿瘤。在用地塞米松预处理后的肾上腺闪烁显像中,肿瘤摄取良好,对侧影像消失。先天性肾上腺皮质增生症患者的CT双侧肾上腺影像均呈线性且明显增大。用电子扇形扫描仪的超声检查能清晰显示增大的右肾上腺,而用电子线阵扫描仪则不能,尽管两种超声仪器对左肾上腺均显示不清。4例接受超声检查的嗜铬细胞瘤患者中,3例被正确检测到,而在其余1例中,肿瘤影像被判定为腹膜后肿瘤。CT也正确显示了前3例嗜铬细胞瘤,但将后1例误诊为胰腺癌。1例肾上腺外嗜铬细胞瘤患者双侧肾上腺对Adosterol摄取良好。4例肾上腺嗜铬细胞瘤中有3例仅显示对侧正常肾上腺的同位素摄取。在另一例右肾上腺嗜铬细胞瘤中,结肠内的同位素积聚使右肾上腺是否有同位素摄取难以判断。