An Interesting Case of MISME Syndrome

Authors

  • Divya Narain Upadhyaya Department of Radiology, Vivekananda Polyclinic and Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
  • Vaishali Upadhyaya Department of Plastic Surgery, King George’s Medical University, Lucknow, Uttar Pradesh, India

Keywords:

meningioma, schwannoma, ependymoma, neurofibromatosis, MRI

Abstract

Multiple inherited schwannomas, meningiomas, and ependymomas (MISME) syndrome or neurofibromatosis type 2 is an autosomal dominant condition characterized by multiple schwannomas, meningiomas, and ependymomas. Bilateral vestibular schwannomas are the hallmark of this condition, which is seen in the majority of patients. Presence of multiple cranial and spinal tumors of different types should alert the radiologist to this possibility so that a timely diagnosis can be made.

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Published

2019-11-13