From the Neuroradiology (R.M., M.C.R.), Sezione di Neuroscienze, Medicine and Surgery Department, University of Salerno, Salerno, Italy
From the Neuroradiology (R.M., M.C.R.), Sezione di Neuroscienze, Medicine and Surgery Department, University of Salerno, Salerno, Italy.
AJNR Am J Neuroradiol. 2017 Oct;38(10):1858-1865. doi: 10.3174/ajnr.A5192. Epub 2017 May 11.
This is the second part of a retrospective and review MR imaging study aiming to define the frequency rate, timing, imaging features, and evolution of gray matter changes in Menkes disease, a rare multisystem X-linked disorder of copper metabolism characterized by early, severe, and progressive neurologic involvement. According to our analysis, neurodegenerative changes and focal basal ganglia lesions already appear in the early phases of the disease. Subdural collections are less common than generally thought; however, their presence remains important because they might challenge the differential diagnosis with child abuse and might precipitate the clinical deterioration. Anecdotal findings in our large sample seem to provide interesting clues about the protean mechanisms of brain injury in this rare disease and further highlight the broad spectrum of MR imaging findings that might be expected while imaging a child with the suspicion of or a known diagnosis of Menkes disease.
这是一项回顾性研究和磁共振成像(MR 成像)研究的第二部分,旨在确定 Menkes 病(一种罕见的多系统 X 连锁铜代谢紊乱疾病,其特征为早期、严重且进行性的神经受累)中灰质变化的频率、时间、影像学特征和演变。根据我们的分析,神经退行性变和局灶性基底节病变已经出现在疾病的早期阶段。硬膜下积液并不像通常认为的那么常见;然而,其存在仍然很重要,因为它们可能会对虐待儿童的鉴别诊断构成挑战,并可能导致临床恶化。我们的大样本中的偶发发现似乎为这种罕见疾病的脑损伤的多形性机制提供了有趣的线索,并进一步强调了在怀疑或已知诊断为 Menkes 病的儿童进行成像时可能预期的广泛的 MR 成像表现。