PDF(Pubmed)
Abstract：
Infantile myofibromatosis (IM) is the most common fibrous disorder of infancy and early childhood. Solitary intracranial involvement is rare and often unrecognized. This makes its early diagnosis and adequate management difficult. The majority of lesions are localized to the skull or dura with variable intracranial extension. Herein, we report a misdiagnosed and aggressive presentation of a solitary IM of the petrous bone. Our aim is to discuss histopathological differential diagnoses and management difficulties.
摘要：
婴儿肌纤维瘤病（IM）是婴儿期和幼儿期最常见的纤维性疾病。孤立性颅内受累是罕见的，通常无法识别。这使得其早期诊断和充分管理变得困难。大多数病变位于颅骨或硬脑膜，颅内延伸可变。在这里，我们报告了岩骨孤立性IM的误诊和积极表现。我们的目的是讨论组织病理学鉴别诊断和管理困难。
