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一例巨大垂体腺瘤伴术后精神障碍最终导致双眼失明的病例。

A Case of Giant Pituitary Adenoma Associated with a Postoperative Mental Disorder That Ultimately Resulted in Bilateral Blindness.

作者信息

Tonari Masahiro, Nishikawa Yuko, Matsuo Junko, Mimura Masashi, Oku Hidehiro, Sugasawa Jun, Ikeda Naokado, Kurisu Yoshitaka, Ikeda Tsunehiko

机构信息

Department of Ophthalmology, Osaka Medical College, Takatsuki-City, Japan.

Department of Neurosurgery, Osaka Medical College, Takatsuki-City, Japan.

出版信息

Case Rep Ophthalmol. 2020 Mar 4;11(1):92-99. doi: 10.1159/000506392. eCollection 2020 Jan-Apr.

Abstract

PURPOSE

To report the case of a patient with adrenocorticotropic hormone (ACTH)-producing pituitary adenoma who developed a mental disorder after initial surgery that kept him from undergoing scheduled follow-up visits and who ultimately had a giant recurrent tumor that resulted in blindness.

CASE REPORT

A 37-year-old male presented with the primary complaint of decreased visual acuity (VA) in both eyes and visual field defects. Visual field examination revealed bitemporal hemianopia. Magnetic resonance imaging (MRI) showed a pituitary tumor of approximately 4 cm in diameter extending from the intrasellar region to the sphenoid sinus and the suprasellar region. Transnasal transsphenoidal surgery was performed. Immunostaining of tumor tissue collected intraoperatively showed ACTH-positive cells, thus leading to the diagnosis of ACTH-producing pituitary adenoma. Postoperatively, the patient reportedly developed mental disorder that possibly interfered with scheduled appointments or continuous follow-up visits for many years, so we had no postoperative data about the vision/visual filed. Seven years later, he presented with markedly decreased VA (i.e., no light perception) in both eyes. Fundus examination showed bilateral marked optic disc atrophy. MRI showed a larger than 8-cm diameter giant recurrent pituitary adenoma in the suprasellar region, for which craniotomy was performed for partial tumor resection. Preoperatively, his blood cortisol level was low, and the lesion was deemed a nonfunctioning pituitary adenoma. Postoperatively, no significant complications occurred, yet his VA was no light perception OD and light perception OS.

CONCLUSIONS

Clinicians should be aware that patients with ACTH-producing pituitary adenomas may develop a mental disorder following surgery and possibly be unable to undergo scheduled follow-up, thus illustrating the importance of establishing an adequate patient follow-up system.

摘要

目的

报告1例促肾上腺皮质激素(ACTH)分泌型垂体腺瘤患者,该患者在初次手术后出现精神障碍,导致其无法按计划进行随访,最终出现巨大复发性肿瘤并导致失明。

病例报告

一名37岁男性,主要症状为双眼视力下降(VA)和视野缺损。视野检查显示双颞侧偏盲。磁共振成像(MRI)显示一个直径约4 cm的垂体肿瘤,从鞍内区域延伸至蝶窦和鞍上区域。行经鼻蝶窦手术。术中收集的肿瘤组织免疫染色显示ACTH阳性细胞,从而诊断为ACTH分泌型垂体腺瘤。据报道,术后患者出现精神障碍,可能干扰了多年来的定期预约或持续随访,因此我们没有术后视力/视野的相关数据。7年后,他双眼视力明显下降(即无光感)。眼底检查显示双侧视神经乳头明显萎缩。MRI显示鞍上区域有一个直径大于8 cm的巨大复发性垂体腺瘤,为此进行了开颅手术以部分切除肿瘤。术前,他的血皮质醇水平较低,该病变被认为是无功能垂体腺瘤。术后未发生明显并发症,但他的视力右眼无光感,左眼仅有光感。

结论

临床医生应意识到,ACTH分泌型垂体腺瘤患者术后可能出现精神障碍,进而可能无法按计划进行随访,这说明了建立完善的患者随访系统的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d43/7154240/836cc16144de/cop-0011-0092-g01.jpg

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