Yamada S, Aiba T, Sano T, Kovacs K, Shishiba Y, Sawano S, Takada K
Department of Neurosurgery, Toranomon Hospital, Tokyo.
Neurosurgery. 1993 Jul;33(1):20-7. doi: 10.1227/00006123-199307000-00003.
In this study, we compared the clinical and endocrinological characteristics, neuroimaging findings, surgical outcome, and conventional histological findings (including immunohistochemistry) with the electron microscopic appearance of 31 growth hormone (GH)-producing adenomas. By electron microscopy, these 31 tumors were divided into 23 densely granulated somatotroph adenomas (DG adenomas) and 8 sparsely granulated somatotroph adenomas (SG adenomas). SG adenomas more frequently affected younger women, but no significant correlation was found between the adenoma type and the characteristic signs and symptoms of acromegaly, the incidence of diabetes mellitus or hypertension, or the basal serum GH and insulin-like growth factor I levels. A distinct response of GH to thyrotropin-releasing hormone, bromocriptine, or GH-releasing hormone was significantly more common in patients with DG adenomas than in those with SG adenomas, whereas the incidence of a response to gonadotropin-releasing hormone or oral glucose was not significantly different between the two groups. An analysis of neuroimaging findings and surgical results indicated that SG adenomas were more likely to be macroadenomas with suprasellar extension or invasive tumors and had a lower surgical cure rate. However, postoperative radiotherapy seemed to be similarly effective in both types of adenoma to prevent a tumor recurrence and to reduce postoperative GH basal level in serum. Light microscopy showed that DG adenomas were mainly acidophilic and were immunopositive not only for GH but also for prolactin (43%), the beta subunit of thyroid-stimulating hormone (26%), and the alpha subunit of glycoprotein hormone (87%), whereas SG adenomas were almost all chromophobic and only revealed immunopositivity for GH.(ABSTRACT TRUNCATED AT 250 WORDS)
在本研究中,我们将31例生长激素(GH)分泌型腺瘤的临床和内分泌学特征、神经影像学表现、手术结果以及传统组织学检查结果(包括免疫组化)与电镜下表现进行了比较。通过电镜检查,这31个肿瘤被分为23个密集颗粒型生长激素细胞腺瘤(DG腺瘤)和8个稀疏颗粒型生长激素细胞腺瘤(SG腺瘤)。SG腺瘤更常累及年轻女性,但腺瘤类型与肢端肥大症的特征性体征和症状、糖尿病或高血压的发病率,或基础血清GH和胰岛素样生长因子I水平之间未发现显著相关性。与SG腺瘤患者相比,DG腺瘤患者中GH对促甲状腺激素释放激素、溴隐亭或生长激素释放激素的明显反应更为常见,而两组对促性腺激素释放激素或口服葡萄糖反应的发生率无显著差异。神经影像学表现和手术结果分析表明,SG腺瘤更可能是具有鞍上扩展的大腺瘤或侵袭性肿瘤,手术治愈率较低。然而,术后放疗在预防两种类型腺瘤的肿瘤复发以及降低血清术后GH基础水平方面似乎同样有效。光镜检查显示,DG腺瘤主要为嗜酸性,不仅对GH免疫阳性,对催乳素(43%)、促甲状腺激素β亚基(26%)和糖蛋白激素α亚基(87%)也免疫阳性,而SG腺瘤几乎均为嫌色性,仅对GH显示免疫阳性。(摘要截断于250字)