Acoustic neuroma classification
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Simrat Sarai, M.D. [2]
Overview
Acoustic neuroma may be classified into three subtypes based MRI, and into four subtypes based on microscopic histopathology.
Classification
Based on the MRI scan, acoustic neuromas can be classified into three subtypes:
- Entirely intracanalicular: The entire tumor is completely within the bony canal.
- Intracranial extension without brain stem distortion.
- Intracranial extension with brain stem distortion.
Based on microscopic histopathology, acoustic neuroma can be classified into four subtypes:[1]
- Conventional schwannoma.
- Cellular schwannoma.
- Plexiform schwannoma.
- Melanotic schwannoma.
- Conventional schwannoma: It is the most common.
- Cellular schwannoma: It may mimic malignant peripheral nerve sheath tumor.
- Plexiform schwannoma: It may mimic malignant peripheral nerve sheath tumor if cellular- especially in childhood.
- Melanotic schwannoma: It may be confused with melanoma.
It is associated with psammomatous form (psammomatous melanotic schwannoma) and with a heritable disorder (Carney complex). The Carney complex, also known as Carney syndrome, NAME syndrome and LAMB syndrome, is a bunch of things that occur together due to some genetic problem. It consists of:
- Cutaneous lentigines
- Myxomas (skin (subcutaneous), subcutanous, heart).
- Endocrine neoplasms[2]
References
- ↑ Kurtkaya-Yapicier O, Scheithauer B, Woodruff JM (2003). "The pathobiologic spectrum of Schwannomas". Histol Histopathol. 18 (3): 925–34. PMID 12792904.
- ↑ "Libre Pathology schwannoma acoustic neuroma subtypes".