Yamaguchi Suguru, Sasajima Toshio, Takahashi Masataka, Kinouchi Hiroyuki, Suzuki Akira, Yoshioka Naomi, Itoh Seiki, Mizoi Kazuo
Department of Neurosurgery, Akita University School of Medicine, 1-1-1 Hondo, Akita-shi, Akita 010-8567, Japan.
No Shinkei Geka. 2004 Sep;32(9):961-7.
We reported a rare case of pleomorphic TSH-producing pituitary adenoma with calcification and reviewed the literature. A 25-year-old female was admitted to our hospital with a complaint of anterior neck swelling. An endocrinological examination demonstrated elevated serum levels of free triiodothyronine (FT3: 5.6 pg/ml), free thyroxin (FT4: 2.2 ng/dl), TSH (5.85 microIU/ml), and TSH a-subunit (5.9 ng/ml), whereas a physical examination revealed no goiter. CT scan showed a suprasellar isodensity mass with dense calcification. Contrast-enhanced T1-weighted images revealed a less enhancing tumor extending from the left upper portion of pituitary fossa into suprasellar cistern. The patient underwent gross total removal of the tumor via the right pterional approach. Microscopically, medium-sized to enlarged tumor cells with marked pleomorphism and prominent calcification were observed. The tumor cells displayed positive reaction for TSH (beta-subunit). The MIB-1 index averaged 2.9%. The histological diagnosis was a pleomorphic TSH-producing pituitary adenoma. Postoperatively, the serum levels of FT3, FT4, TSH, and TSH alpha-subunit decreased to normal range. Follow-up MR images showed no evidence of recurrent tumor 3 years after the resection. All of six patients with densely calcified TSH-producing pituitary adenoma, previously reported in the literature, remained well without tumor recurrence. We suggest that this type of TSH-producing pituitary adenoma may be associated with favorable prognosis despite histologically pleomorphic appearance.
我们报告了一例罕见的伴有钙化的多形性促甲状腺激素分泌型垂体腺瘤病例,并对相关文献进行了回顾。一名25岁女性因前颈部肿胀主诉入院。内分泌检查显示血清游离三碘甲状腺原氨酸(FT3:5.6 pg/ml)、游离甲状腺素(FT4:2.2 ng/dl)、促甲状腺激素(TSH:5.85 μIU/ml)和促甲状腺激素α亚基(5.9 ng/ml)水平升高,而体格检查未发现甲状腺肿大。CT扫描显示鞍上等密度肿块伴致密钙化。增强T1加权图像显示肿瘤强化程度较低,从垂体窝左上部延伸至鞍上池。患者通过右侧翼点入路接受了肿瘤全切术。显微镜下,观察到中等大小至增大的肿瘤细胞,具有明显的多形性和显著钙化。肿瘤细胞对促甲状腺激素(β亚基)呈阳性反应。MIB-1指数平均为2.9%。组织学诊断为多形性促甲状腺激素分泌型垂体腺瘤。术后,FT3、FT4、TSH和促甲状腺激素α亚基的血清水平降至正常范围。随访磁共振图像显示切除术后3年无肿瘤复发迹象。文献中先前报道的所有6例伴有致密钙化的促甲状腺激素分泌型垂体腺瘤患者均情况良好,无肿瘤复发。我们认为,尽管这种促甲状腺激素分泌型垂体腺瘤在组织学上具有多形性外观,但可能与良好的预后相关。