Ogawa Yoshikazu, Tominaga Teiji
Department of Neurosurgery, Kohnan Hospital, 4-20-1 Nagamachiminami, Taihaku-ku, Sendai, Miyagi, 982-8523, Japan.
J Neurooncol. 2008 Mar;87(1):91-5. doi: 10.1007/s11060-007-9492-2. Epub 2007 Nov 7.
Thyrotroph cell adenoma accounts for only 1% of all pituitary adenomas. This tumor is tough and firm because of significant interstitial fibrosis, and is difficult to remove. Atypical adenoma has an aggressive biological character, invades the surrounding structures, and grows rapidly. Atypical thyrotroph cell adenoma is extremely rare.
A 32-year-old man presented with hyperthyroidism and bitemporal hemianopsia. Head magnetic resonance imaging revealed a large sellar tumor compressing the optic chiasma and invading the left cavernous sinus.
Transsphenoidal surgery was performed and subtotal removal was achieved. Histological examination showed atypical thyrotroph cell adenoma. Gamma knife surgery was planned, but the tumor re-grew within 3 months, and reattached to the optic chiasma. Second transcranial surgery failed to remove residual tumor behind the pituitary stalk. Conventional irradiation followed by octreotide administration resulted in decreased tumor size and stable euthyroidism. The tumor has been controlled for 22 months since first surgery and diagnosis.
Atypical thyrotroph cell adenoma has an aggressive biological character and grows rapidly. Multimodal treatment including medication and radiotherapy is required.
促甲状腺素细胞腺瘤仅占所有垂体腺瘤的1%。由于显著的间质纤维化,该肿瘤质地坚韧,难以切除。非典型腺瘤具有侵袭性生物学特性,侵犯周围结构且生长迅速。非典型促甲状腺素细胞腺瘤极为罕见。
一名32岁男性出现甲状腺功能亢进和双颞侧偏盲。头部磁共振成像显示鞍区有一巨大肿瘤,压迫视交叉并侵犯左侧海绵窦。
进行了经蝶窦手术,实现了次全切除。组织学检查显示为非典型促甲状腺素细胞腺瘤。计划进行伽玛刀手术,但肿瘤在3个月内复发,并重新附着于视交叉。第二次经颅手术未能切除垂体柄后方的残留肿瘤。常规放疗后给予奥曲肽,肿瘤体积减小,甲状腺功能正常状态稳定。自首次手术和诊断以来,肿瘤已得到控制22个月。
非典型促甲状腺素细胞腺瘤具有侵袭性生物学特性且生长迅速。需要包括药物治疗和放疗在内的多模式治疗。