Introduction:
This tumor
arises from the olfactory nerve. These are rare malignant tumors
arising from the olfactory epithelium situated at the roof of the
nasal cavity, cribriform plate, upper portion of supeior turbinate
and corresponding upper portion of nasal septum. These tumors
typically involve the upper portion of nasal cavity and the
cribriform plate area. These tumors classically arise from the basal
cells of olfactory neuroepithelium. No clearl cut genetic / other
causes have been attributed for this tumor. This tumor represents
about 3% of all malignant tumors involving the nasal cavity.
This tumor
was first reported by Berger etal in 1924. Since then only less than
1000 cases have been reported in literature.
Incidence:
Affects both
male and female patients with equal frequency.
Age incidence
shows a bimodal peak (peaking at the second and the sixth decades of
life).
Etiopathogenesis
(theories):
- Belongs to peripheral neuroectodermal family. (Not supported by immunohistochemistry)
- Presence of Trisomy 8 has been documented in these tumor cells
None of these
theories convincingly explain etiopathogenesis of this tumor.
Clinical
features:
This tumor
classically involves the nasal cavity with extension into the ethmoid
sinus, anterior skull base and orbit. Since these tumors are very
aggressive ones they tend to metastasize extensively. Spread to
cervical nodes are common. Retropharyngeal nodes are the first
echelon node. Rarely these tumors may be active in an endocrine
sense. These tumors have known to cause ectopic secretion of ACTH
causing Cushing's syndrome.
Common
presenting symptoms were usually associated with the nasal cavity:
- Nasal block
- Epistaxis
- Anosmia
Staging system:
Staging a tumor
helps in deciding the optimal management modality and also in
determining the prognosis of the disease.
Kadish staging
system:
This system
stages Esthesioneuroblastoma into three stages:
Stage A: Tumor
limited to nasal cavity
Stage B: Tumor
extending to paranasal sinuses
Stage C: Tumor
extending beyond paranasal sinuses
Major
inadequacy of this staging system is too broad a staging at the level
of Stage C.
Modified TNM
staging system:
Tumor
T1 – tumor
involving nasal cavity and / or paranasal sinuses (excluding
sphenoid) sparing most of the superior ethmoidal cells
T2- tumor
involving nasal cavity and / or paranasal sinuses including sphenoid
with extension to the cribriform plate
T3 – tumor
extending to orbit with involvement of extradural anterior cranial
fossa
T4 – tumor
involving brain
Node
N0 – No nodal
metastasis
N1 – any form
of nodal metastasis
Metastasis
M0 – No
metastasis
M1 –
Metastasis present
Hyam came out
with a histopathological grading system which turned out to be more
accurate than the preceding two staging systems.
Hyam's
Histopathological grading system
Grade
|
LA preservation
|
Mitotic index
|
Nuclear polymorphism
|
Fibrillary matrix
|
Rosettes
|
Necrosis
|
I
|
+
|
Zero
|
None
|
Prominent
|
HW
|
None
|
II
|
+
|
Low
|
Low
|
Present
|
HW
|
None
|
III
|
+/-
|
Moderate
|
Moderate
|
Low
|
FW
|
Rare
|
IV
|
+/-
|
High
|
High
|
Absent
|
None
|
Frequent
|
Fw –
Flexner-wintersteiner
HW – Homer –
Wright
Management:
This tumor is
managed with wide surgical resection with adequate tumor margins.
Radiotherapy is indieated as primary treatment modality in
unresectable tumors and as a follow up to surgical debulking.
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