Schwannoma
|  | 
| Schwannoma | 
Schwannoma is a benign peripheral nerve
sheath tumor. 
Schwannomas are usually solitary.
Cell of origin of Schwannoma -
Differentiated Schwann cells.
Pathologically Schwannomas are unique,
because  schwannomas do not infiltrate
the parent nerve. 
Surgical significance of this unique
feature is that schwannoma  can  be  enucleated  in toto by preserving  the adjacent nerve. 
|  | 
| Longitudinal Incision | 
Histological characteristics of schwannoma
– Areas of cellular component (Antoni A) and areas of hypocellular component
(Antoni B).
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Most Important Differential Diagnosis of
schwannoma is Neurofibroma.
Neurofibromas are usually multiple.
Cell of origin of Neurofibroma- Transformed
Schwann cells.
Pathologically neurofibroma infiltrates
the parent nerve. 
Surgical significance – Neurofibroma is  resected along with the parent nerve and  nerve 
grafting is done  to  preserve the nerve function
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Discussion on Neurofibromatosis
Two Types of Neurofibromatosis- Type
1& Type 2
Type 1 Neurofibromatosis is associated
with
Café
au lait patches
Lisch
nodules
Optic
glioma
Type 2 Neurofibromatosis is associated
with 
Bilateral
acoustic neuromas
Meningioma
 Mesothelioma
Glioma
multiforme
Carcinoma
of Breast
Carcinoma
Colorectum, 
 Renal
Cell Carcinoma
Hepato
Cellular Carcinoma
Prostatic
Carcinoma
Cutaneous
malignancy
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 Image Courtesy- Trivandrum Surgical Club
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