Wednesday, 16 November 2011

Esthesioneuroblastoma


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):

  1. Belongs to peripheral neuroectodermal family. (Not supported by immunohistochemistry)
  2. 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:

  1. Nasal block
  2. Epistaxis
  3. 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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