Department of Neurosurgery, New York Presbyterian Hospital, Weill Cornell Medical College, Box 99, 525 East 68th St., New York, NY, 10065, USA.
Department of Otolaryngology, New York Presbyterian Hospital, Weill Cornell Medical College, Box 99, 525 East 68th St., New York, NY, 10065, USA.
Pituitary. 2017 Dec;20(6):702-708. doi: 10.1007/s11102-017-0826-6.
Double adenomas in the pituitary gland are a rare occurrence. The ability to cure a hormone-producing adenoma with surgery is dependent on the ability to identify and completely remove the correct adenoma. The relative frequency of each subtype of hormone-secreting adenomas confirmed with magnetic resonance image (MRI), surgery and immunohistochemistry is not defined.
Following PRISMA guidelines, we performed a systematic review of PubMed Central, Google Scholar, Scopus Database, Cochrane database and Science Research, using the key-words: "double pituitary adenomas", "multiple pituitary adenomas" and only papers where multiple or truly separate double pituitary adenomas were identified pre-surgically by MRI and/or confirmed by pathology/immunohistochemistry staining were included.
We reviewed papers from 1975 to 2016 and found 17 cases with two pituitary adenomas and 1 with three pituitary adenomas. The ages ranged from 22 to 67 years old, and there were twelve females and five males. Immunohistochemical staining showed that the most common double pituitary adenomas were growth hormone (GH)- followed by adrenocorticotropic (ACTH)-secreting.
Double pituitary adenomas are rare but most commonly found with GH- or ACTH-producing tumors. It is critical to remove all identified possible adenomas to achieve biochemical cure and clinicians should have heightened sensitivity in patients with acromegaly or Cushing's Disease.
垂体双腺瘤是一种罕见的情况。通过手术治愈激素分泌腺瘤的能力取决于识别和完全切除正确腺瘤的能力。经磁共振成像(MRI)、手术和免疫组织化学证实的每种激素分泌腺瘤亚型的相对频率尚未确定。
我们遵循 PRISMA 指南,在 PubMed Central、Google Scholar、Scopus 数据库、Cochrane 数据库和科学研究中进行了系统评价,使用的关键词是:“垂体双腺瘤”、“多发性垂体腺瘤”,仅包括术前通过 MRI 识别出多个或真正独立的垂体双腺瘤,并通过病理/免疫组织化学染色证实的论文。
我们回顾了 1975 年至 2016 年的论文,发现有 17 例有两个垂体腺瘤,1 例有三个垂体腺瘤。年龄从 22 岁到 67 岁不等,其中女性 12 例,男性 5 例。免疫组织化学染色显示,最常见的垂体双腺瘤是生长激素(GH)-其次是促肾上腺皮质激素(ACTH)-分泌。
垂体双腺瘤虽然罕见,但最常见于 GH 或 ACTH 分泌性肿瘤。切除所有已识别的可能腺瘤对于实现生化治愈至关重要,临床医生应在患有肢端肥大症或库欣病的患者中提高敏感性。