Nishioka H, Akada K, Akimoto J, Ito H
Department of Neurosurgery, Tokyo Medical College, Japan.
No To Shinkei. 1993 Nov;45(11):1019-25.
We compared clinical features, including endocrinological and radiological findings, histological features and the proliferative parameters (PCNA, MIB-1 and AgNORs) with immunohistochemical features in growth hormone (GH) secreting pituitary adenomas. 18 cases were divided into two groups based on immunohistochemical intracytoplasmic stainings for cytokeratin: a prominent dot-like pattern (group I, 6 cases) and a diffuse perinuclear pattern (group II, 12 cases). Patients in group I (6 females, m = 37.6 years old) were younger, showed female predominance and had a shorter history of acromegaly compared with patients in group II (7 males, 5 females, m = 44.9 years old). Although the size of the adenomas tend to be larger in group I, no difference was recognized in plasma GH levels between the two groups. Increased serum prolactin (PRL) levels were accompanied more common in group I. Abnormal GH responses to TRH and LHRH injection and GH suppressions to bromocriptine administration were more frequently noted in group II than group I. Surgical approaches were transcranial in most cases of group I and transphenoidal in group II. There was no difference in surgical results as to the correction rate of GH levels between the two groups. Histopathologically, group I adenomas were mostly chromophobic, weakly positive for GH, and were generally negative for PRL and alpha-subunit. On the other hand, group II adenomas were mostly acidophilic, diffusely stained for GH, and were often positive for PRL and alpha-subunit. However, there was no significant difference in proliferating parameters between the two groups.(ABSTRACT TRUNCATED AT 250 WORDS)
我们比较了生长激素(GH)分泌型垂体腺瘤的临床特征(包括内分泌和放射学检查结果)、组织学特征以及增殖参数(增殖细胞核抗原、MIB-1和核仁组成区嗜银蛋白)与免疫组化特征。18例患者根据细胞角蛋白免疫组化胞浆染色分为两组:显著点状模式(I组,6例)和弥漫性核周模式(II组,12例)。与II组患者(7例男性,5例女性,平均年龄44.9岁)相比,I组患者(6例女性,平均年龄37.6岁)更年轻,以女性为主,肢端肥大症病史更短。虽然I组腺瘤的大小往往更大,但两组间血浆GH水平无差异。I组血清催乳素(PRL)水平升高更为常见。II组比I组更频繁地出现GH对促甲状腺激素释放激素(TRH)和促黄体生成素释放激素(LHRH)注射反应异常以及对溴隐亭给药的GH抑制。I组大多数病例采用经颅手术入路,II组采用经蝶手术入路。两组间GH水平校正率的手术结果无差异。组织病理学上,I组腺瘤大多为嫌色性,GH弱阳性,PRL和α亚单位通常为阴性。另一方面,II组腺瘤大多为嗜酸性,GH弥漫性染色,PRL和α亚单位常为阳性。然而,两组间增殖参数无显著差异。(摘要截断于250字)