Bou-Nassif R, El Ahmadieh T Y, Abou-Mrad Z, Rosenblum M, Cohen M A, Tabar V
Department of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, USA; Multidisciplinary Pituitary and Skull Base Tumor Program, Memorial Sloan Kettering Cancer Center, New York, USA.
Department of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York, USA; Multidisciplinary Pituitary and Skull Base Tumor Program, Memorial Sloan Kettering Cancer Center, New York, USA.
Neurochirurgie. 2023 Mar;69(2):101404. doi: 10.1016/j.neuchi.2023.101404. Epub 2023 Jan 24.
Adamantinomatous craniopharyngioma has a bimodal age distribution occurring in children aged 5-15 years and less frequently in adults aged 45-60 years. The current embryogenetic hypothesis suggests that adamantinomatous craniopharyngioma (ACP) arises from epithelial remnants of the craniopharyngeal duct or Rathke's pouch. It is thought that this tumor exists early on during childhood but remains indolent, growing very slowly until it is diagnosed incidentally or due to symptoms. Recent reports of de novo development of ACP, however, have challenged this theory. Herein, we present a case of an incidentally discovered de novo adamantinomatous craniopharyngioma that was documented to arise de novo on serial MRIs performed for a different indication. To our knowledge, this is the first report of a middle-aged patient who is diagnosed with a de novo ACP documented with contrast-enhanced MRIs of the sella over a 16-year period. This case challenges our current understanding of the pathophysiology of adamantinomatous craniopharyngioma.
造釉细胞瘤型颅咽管瘤具有双峰年龄分布,好发于5至15岁的儿童,较少见于45至60岁的成年人。目前的胚胎发生假说认为,造釉细胞瘤型颅咽管瘤(ACP)起源于颅咽管或Rathke囊的上皮残余。据认为,这种肿瘤在儿童早期就已存在,但生长缓慢,直到偶然被诊断或因出现症状才被发现。然而,最近关于ACP新发的报道对这一理论提出了挑战。在此,我们报告一例偶然发现的新发造釉细胞瘤型颅咽管瘤,该病例经连续MRI检查证实为新发,最初的MRI检查是针对其他指征进行的。据我们所知,这是首例在16年期间通过鞍区增强MRI确诊为新发ACP的中年患者。该病例对我们目前对造釉细胞瘤型颅咽管瘤病理生理学的理解提出了挑战。