Akkus Gamze, Odabaş Fulya, Sözütok Sinan, Sert Murat, Ak Numan Emre, Evran Mehtap, Tetiker Tamer
Division of Endocrinology, Cukurova University, Adana, Turkey.
Division of Radiology, Cukurova University, Adana, Turkey.
Horm Metab Res. 2022 Jan;54(1):37-41. doi: 10.1055/a-1685-0655. Epub 2021 Nov 29.
According to the recent studies, immunohistochemical subtypes of growth hormone (GH) secreting adenomas have been considered as a predictive factor in determining the clinical outcomes including biochemical, radiologic, and endocrine remission. In a 20 year-of time period, acromegaly patients who were treated and followed at the Endocrinology Department of our University Hospital were screened for the study. Of total 98 patients, 65 patients who had been operated by transsphenoidal surgery and having postoperative specimens were included. Postoperative specimens of the surgery of the patients were classified into 3 groups based on the histochemical characteristics (densely, sparsely, and mixed). Parasellar extensions of pituitary tumors were classified into the five grades according to Knosp classification. The patients were investigated and evaluated for postoperative clinical progress, remission rates, comorbidities regarding with the histopathological patterns. Of total 65 patients, 31 were classified as densely granulated (group 1), 32 were classified as sparsely granulated (group 2), and 2 patients were assessed as mixed granulated (group 3). There was no difference between groups for age and gender. Pre-treatment of adenoma size in all groups was correlated with each other and the frequency of macroadenoma (1 vs. 2, 77.4 vs. 84.3%) was higher in two groups. Although mean initial GH levels in group 1 was higher than the other groups (p=0.03), IGF1 levels (age and gender matched) were similar in each group. Adenomas in all groups demonstrated noninvasive radiological characteristics (Knosp grade 0-1-2). Ki-67 proliferation index of both groups (64.5 vs. 50%) was predominantly 1%. With a similar follow-up period, the endocrine remission rates (GH<1 μg/l) in groups were 64 vs. 69%, respectively. In conclusion, classification according to immunohistochemical subtypes of growth hormone secreting adenomas may not be a qualified parameter to evaluate patients with patterns of aggressiveness, clinical outcomes, or treatment response.
根据最近的研究,生长激素(GH)分泌性腺瘤的免疫组织化学亚型已被视为决定包括生化、放射学和内分泌缓解在内的临床结果的一个预测因素。在20年的时间段内,对在我们大学医院内分泌科接受治疗和随访的肢端肥大症患者进行了研究筛选。在总共98例患者中,纳入了65例接受经蝶窦手术且有术后标本的患者。根据组织化学特征(密集型、稀疏型和混合型)将患者手术的术后标本分为3组。垂体肿瘤的鞍旁扩展根据Knosp分类分为五个等级。对患者的术后临床进展、缓解率、与组织病理学模式相关的合并症进行了调查和评估。在总共65例患者中,31例被分类为密集颗粒型(第1组),32例被分类为稀疏颗粒型(第2组),2例被评估为混合颗粒型(第3组)。各组之间在年龄和性别方面没有差异。所有组腺瘤大小的预处理相互关联,两组中巨大腺瘤的发生率较高(1级对2级,77.4%对84.3%)。虽然第1组的平均初始GH水平高于其他组(p = 0.03),但各组中(年龄和性别匹配的)IGF1水平相似。所有组的腺瘤均表现出非侵袭性放射学特征(Knosp 0 - 1 - 2级)。两组的Ki - 67增殖指数(64.5%对50%)主要为1%。在相似的随访期内,各组的内分泌缓解率(GH < 1μg/l)分别为64%和69%。总之,根据生长激素分泌性腺瘤的免疫组织化学亚型进行分类可能不是评估具有侵袭性模式、临床结果或治疗反应的患者的一个合格参数。