Coexisting Non-functioning Pituitary Macroadenoma and Sellar-Suprasellar Lipoma: A Case Report and Literature Review.

Q4 Medicine
Acta Medica Philippina Pub Date : 2025-01-31 eCollection Date: 2025-01-01 DOI:10.47895/amp.vi0.7564
Jereel Aron R Sahagun, Edrome F Hernandez, Mark Anthony S Sandoval
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引用次数: 0

Abstract

Intracranial lipomas are benign tumors that may occasionally be found in the suprasellar cistern while pituitary adenomas are far more common brain tumors. Pituitary adenomas may rarely coexist with other intracranial tumors in the sellar-suprasellar region. We share a unique case of a patient with coexisting non-functioning pituitary adenoma and sellar-suprasellar lipoma presenting with blurring of vision. We report a 55-year-old male presenting with a two-year history of blurring of vision with findings of a 2.7 x 3.0 x 3.2 cm homogeneously enhancing lobulated isointense mass on the sellar-suprasellar region. Hormonal workups revealed low cortisol and mildly elevated prolactin. He initially underwent endonasal transsphenoidal excision of the tumor which revealed to be a lipoma on histopathology. Due to minimal improvement of vision from the subtotal excision, he underwent repeat surgery through the transcranial approach which in turn showed a pituitary adenoma. The co-occurrence of two sellar-suprasellar tumors with different histology is rare, as most of the evidence is based on only a handful of case series. Intracranial lipomas result from persistence and abnormal differentiation of the meninx primitiva during the development of the subarachnoid cisterns. On the other hand, pituitary tumorigenesis is still largely unclear but appears to involve multiple tumor suppressor genes, oncogenes, cell cycle deregulation factors, and miRNAs. Given the differing pathogenesis of each tumor type, the coexistence may only be coincidental. The best surgical approach in this situation is unknown but the focus is on complete excision of the adenoma.

无功能垂体大腺瘤与鞍上脂肪瘤共存1例并文献复习。
颅内脂肪瘤是良性肿瘤,偶尔见于鞍上池,而垂体腺瘤是更为常见的脑肿瘤。垂体腺瘤很少与鞍上区其他颅内肿瘤共存。我们分享一个独特的病例,患者共存无功能垂体腺瘤和鞍上脂肪瘤表现为视力模糊。我们报告一名55岁男性患者,有两年的视力模糊史,发现在鞍上区有一个2.7 x 3.0 x 3.2 cm均匀增强的分叶状等强度肿块。激素检查显示皮质醇低,泌乳素轻度升高。他最初接受鼻内经蝶窦切除肿瘤,病理结果显示为脂肪瘤。由于次全切除对视力的改善很小,他通过经颅入路再次接受手术,结果显示垂体腺瘤。两种不同组织学的鞍上肿瘤同时发生是罕见的,因为大多数的证据都是基于少数的病例系列。颅内脂肪瘤是由蛛网膜下腔池发育过程中原始脑膜的持续和异常分化引起的。另一方面,垂体肿瘤的发生仍不清楚,但似乎涉及多种肿瘤抑制基因、癌基因、细胞周期调节因子和mirna。鉴于每种肿瘤类型的发病机制不同,共存可能只是巧合。在这种情况下最好的手术方法是未知的,但重点是完全切除腺瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Medica Philippina
Acta Medica Philippina Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
199
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