Asuzu David T, Burke Rebecca M, Hakim Jeffrey, Coss Dylan, Park Min S, Payne Spencer C, Jane John A
Department of Neurosurgery.
Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland.
J Neurosurg Case Lessons. 2021 Mar 8;1(10):CASE2122. doi: 10.3171/CASE2122.
Giant pituitary macroadenomas with a diameter >4 cm are rare tumors, accounting for only about 5% of pituitary adenomas. They are more difficult to maximally resect safely owing to limited access as well as encasement of adjacent structures. Acidophil stem cell adenomas are rare immature neoplasms proposed to derive from common progenitor cells of somatotroph and lactotroph cells. These adenomas comprise about 4.3% of surgically removed pituitary adenomas. No previous reports have described acidophil stem cell adenomas that grow to the size of giant macroadenomas. This rare entity poses special challenges given the need for maximal safe resection in an immature neoplasm.
The authors report a 21-year-old female who presented with 3 years of progressive visual decline and a giant macroadenoma. She underwent endoscopic transsphenoidal surgery for decompression. Given the tumor size and involvement of adjacent critical structures, gross-total resection was not achieved. The authors review the literature on giant pituitary adenomas and provide a discussion on clinical management for this rare entity.
The authors present a very rare case of a giant pituitary adenoma of acidophil stem cell origin and discuss the technical and management challenges in this rare entity.
直径大于4厘米的巨大垂体大腺瘤是罕见肿瘤,仅占垂体腺瘤的约5%。由于手术入路受限以及相邻结构被包裹,此类肿瘤更难实现安全的最大程度切除。嗜酸干细胞腺瘤是罕见的未成熟肿瘤,被认为起源于生长激素细胞和催乳素细胞的共同祖细胞。这些腺瘤约占手术切除垂体腺瘤的4.3%。此前尚无关于生长至巨大腺瘤大小的嗜酸干细胞腺瘤的报道。鉴于需要在未成熟肿瘤中进行最大程度的安全切除,这种罕见实体带来了特殊挑战。
作者报告了一名21岁女性,她因3年渐进性视力下降就诊,被诊断为巨大垂体大腺瘤。她接受了内镜经蝶窦手术减压。鉴于肿瘤大小及相邻关键结构受累情况,未能实现全切除。作者回顾了关于巨大垂体腺瘤的文献,并对这种罕见实体的临床管理进行了讨论。
作者展示了一例极为罕见的嗜酸干细胞起源的巨大垂体腺瘤病例,并讨论了这种罕见实体在技术和管理方面的挑战。