Schwannoma
The Common vein Copyright 2010
Definition
A Schwannomas is characterized as a benign tumor arising from the perineural Schwann cells.
They most often affect the vestibular division of cranial nerve VIII but can involve other cranial nerves as well, commonly the trigeminal or facial nerves. They are the second most common extra-axial mass in adults. Generally these are slow growing low grade tumors. Occasionally they may grow to be quite large and exhibit mass effect on the brainstem. Malignant degeneration is infrequent. Bilateral vestibular schwannomas are diagnostic of neurofibromatosis type two.
Histologically schwannomas are encapsulated masses attached to the nerve but can be dissected from it, unlike neurofibromas, another type of peripheral nerve sheath tumor. There are two classic growth patterns, Antoni A and Antoni B. In Antoni A there are densely packed elongated cells arranged in fascicles. The Antoni B pattern is made up of a loose meshwork of cells, microcysts and myxoid stroma.
Common symptoms of this tumor include sensineural hearing loss, vertigo and tinnitus.
Schwannomas can be imaged by CT however MRI is more sensitive for detection. On CT they appear isodense to the cerebellum. On MRI they may appear as a T1 isointense to hypointense and T2 hyperintense mass. Schwannomas enhance homogeneously, but may enhance heterogeneously and demonstrate areas of cystic degeneration and punctuate calcifications.
Treatment options include microsurgical resection or radiosurgery. Depending on patient symptoms and lesion size, they may be simply observed over time by serial imaging.
Acoustic Neuroma |
Image Courtesy Elisa Flower MD and Asim Mian MD 97681c.8 |
H&E Low Power
H&E High Power
H&E High Power Schwannoma |
Image Courtesy of Cheryl Spencer, M.A. and Ivana Delalle, MD, PhD Department of Pathology Boston University School of Medicine 98521 98522 98523 |
References
Robbins Pathology