Author:
Bakhtiar Yuriz,Hirano Hirofumi,Arita Kazunori,Yunoue Shunji,Fujio Shingo,Tominaga Atsushi,Sakoguchi Tetsuhiko,Sugiyama Kazuhiko,Kurisu Kaoru,Yasufuku-Takano Junko,Takano Koji
Abstract
ObjectiveSomatotropinomae are classified as densely and sparsely granulated adenomae, which typically exhibit a perinuclear pattern (PP) and a dot pattern (DP) in cytokeratin (CK) immunostaining respectively. Some exhibit a mixed pattern (MP). We studied the relationship between these somatotropinoma subtypes and their clinico-pathological features.MethodsThe study population consisted of 141 Japanese acromegalic patients. We evaluated their clinical presentation and their response to provocation tests with TRH and LHRH and to suppression (octreotide) test. Tumour tissues were subjected to immunostaining for CAM-5.2, MIB-1, CD34, E-cadherin (CDH1) and p53 (TP53). In 43 cases (30 non-DP and 13 DP), we analysedgspmutations (constitutively activating mutations of the Gsα protein that is encoded byGNASgene).ResultsThe 141 adenomae were categorised into three subtypes based on their CK staining patterns; 30 (21.3%) exhibited DP, 83 (58.9%) exhibited PP, and 28 (19.9%) exhibited MP. Compared with the other subtypes, DP adenomae were significantly larger, and their E-cadherin expression and response to TRH, LHRH and octreotide challenge were lower. The postoperative cure rate tended to be lower in DP adenomae.gspmutations were detected in 25 of 43 cases examined (58.1%); 20 of the 30 non-DP (66.7%) and 5 of the 13 DP tumours (38.5%) were affected by the mutation.ConclusionDP somatotropinomae exhibit characteristic features. Compared with the non-DP subtypes, DP adenomae manifested a larger tumour size, a lower incidence of abnormal responses to TRH and LHRH challenge, a poor response to octreotide test and a lower expression of E-cadherin.gspmutation was not exclusive for non-DP somatotropinomae.
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
82 articles.
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