Kessler L, Legaludec V, Dietemann J L, Maitrot D, Pinget M
Service d'Endocrinologie et Maladies Métaboliques, Hôpital Central, Strasbourg, France.
Neurosurg Rev. 1999 Dec;22(4):222-5. doi: 10.1007/s101430050021.
This report concerns one case of a sphenoid sinus mucocele occurring 17 years after transsphenoidal surgery for acromegaly. In 1979, a 51-year-old man was successfully operated by the transnasal transsphenoidal approach for a growth hormone (GH) adenoma 1 cm in diameter. In 1996, the patient was hospitalized for headaches and diplopia. He presented a loss of right visual acuity with paralysis of the right oculomotor nerve. The basal GH level was normal with a satisfactory decrease after oral glucose ingestion. Pituitary sellar radiography showed a disappearance of the posterior clinoid while magnetic resonance imaging revealed the existence of a bilocular, circular, homogeneous lesion of the sphenoid sinus 3 cm in diameter with a posterior and lateral extension. The diagnosis of mucocele was confirmed by surgical treatment, allowing drainage of the mucocele through a transsphenoidal approach. The drained material was composed of sinus epithelium containing many polynuclear and resorptive cells. Postoperatively, the symptoms decreased dramatically, leading to full recovery of visual function and disappearance of the headaches. Apart from the tumor recurrence, the mucocele of the sphenoid sinus can be evoked as a possible long term complication of transsphenoidal surgery for pituitary adenoma.
本报告涉及1例垂体瘤经蝶窦手术后17年发生的蝶窦黏液囊肿。1979年,一名51岁男性经鼻蝶窦入路成功切除直径为1 cm的生长激素(GH)腺瘤。1996年,该患者因头痛和复视住院。他出现右眼视力丧失及右侧动眼神经麻痹。基础GH水平正常,口服葡萄糖后下降良好。垂体蝶鞍部X线片显示后床突消失,而磁共振成像显示蝶窦存在一个直径3 cm的双腔、圆形、均匀性病变,向后外侧延伸。黏液囊肿的诊断经手术治疗得以证实,通过经蝶窦入路排出了黏液囊肿。排出物由含有许多多核及吸收细胞的鼻窦上皮组成。术后,症状显著减轻,视觉功能完全恢复,头痛消失。除肿瘤复发外,蝶窦黏液囊肿可被视为垂体腺瘤经蝶窦手术可能的长期并发症。