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CLASSIFICATION
1)Primary Tumours:
Benign Glomus tumour
Malignant Carcinoma ,sarcoma
2)Secondary Tumours:
a) From adjacent areas like nasopharynx ,
external meatus and parotid.
b)Metastatic eg. From ca of bronchus,
breast, thyroid, prostrate, GIT.
GLOMUS TUMOUR:
 Most common benign neoplasm of middle
ear and originate from the glomus bodies .
It is found in the jugular bulb or on the
promontory along course of tympanic
branch of IXth cranial nerve(jacobson’s
nerve).
 The tumour consists of paraganglionic cells
derived from the neural crest.
AETIOLOGY AND
PATHOLOGY
 Often seen in middle age.(40-50).
 Females>Males.
 It is a benign non encapsulated but
extremely vascular ,slow growing and locally
invasive tumours.
 Microscopically it shows sheets of epithelial
cells with large nuclei and granular
Two types of glomus tumours:
1)Glomus jugulare: They arise from dome of jugular
bulb, invade hypotympanum and jugular foramen ,
causing neurological sign of IX th to XII th cranial
nerve involvement . They may compress or invade
lumen of jugular vein.
2)Glomus Tympanicum: They arise from promontory
of middle ear.
CLINICAL
FEATURES:
 A)When tumour is intratympanic:
• Earliest symptoms are deafness and
tinnitus.Deafness is conductive type and tinnitus
is pulsatile.
• Otoscopy show red reflex through intact TM.
“Rising sun”appearance is seen.
• “Pulsation sign”(Brown’s sign) is positive.
B) When tumour present as polyp: profuse bleeding
from ear either spontaneously or after cleaning.
• Dizziness or vertigo and facial paralysis may
appear . Earache less common otorrhoea due to
secondary infection.Examionation reveals red
vascular polyp.
 Cranial nerve palsies: It is a late feature .IX
th to XII cranial nerves may be
involved.dysphagia , hoarsness with
unilateral paralysis of soft palate, pharynx
and vocal cord.
 Tumours may present as mass over mastoid
or in nasopharynx.
 Audible bruit over mastoid.
 Some glomus tumours secrete
catecholamines and produce their
symptoms.
DIAGNOSIS:
1)CT scan head
2)MRI
3)Four vessel angiography
TREATMENT:
 Surgical removal
 Radiation
 Embolisation
 Combination of the above techniques
CARCINOMA OF MIDDLE EAR AND
MASTOID
AETIOLOGY:
Age- 40 to 60, females>males, chronic
irritation may be the cause.
PATHOLOGY:
Tumour may arise primarily from middle ear
or be an extension of carcinoma of deep
meatus. Squamous cell variety is most
common.
CLINICAL FEATURES:
 CHRONIC FOUL SMELLING DISCHARGE SPECIALLY
BLOOD STAINED.
 PAIN USUALLY SEVER AND COMES AT NIGHT
 FACIAL PALSY
 FRIABLE HAEMORRHAGIC GRANULATIONS OR POLYP
 APPEARANCE OF OR INCREASE IN DEAFNESS OR
VERTIGO.
DIAGNOSIS
 DEFINITIVE DIAGNOSIS IS MADE ONLY
ON BIOPSY
 EXTENT OF DISEASE IS JUDGED BY
CLINICAL AND RADIOLOGICAL
EXMINATION.
 CT SCAN & ANGIOGRAPHY ARE
USEFUL IN THE ASSESSMENT OF
DISEASE.
TREATMENT:
 Combination of surgery and radiotherapy
gives better results.
THANK YOU

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Tumours of middle ear and mastoid.pptx

  • 1.
  • 2. CLASSIFICATION 1)Primary Tumours: Benign Glomus tumour Malignant Carcinoma ,sarcoma 2)Secondary Tumours: a) From adjacent areas like nasopharynx , external meatus and parotid. b)Metastatic eg. From ca of bronchus, breast, thyroid, prostrate, GIT.
  • 3. GLOMUS TUMOUR:  Most common benign neoplasm of middle ear and originate from the glomus bodies . It is found in the jugular bulb or on the promontory along course of tympanic branch of IXth cranial nerve(jacobson’s nerve).  The tumour consists of paraganglionic cells derived from the neural crest.
  • 4.
  • 5. AETIOLOGY AND PATHOLOGY  Often seen in middle age.(40-50).  Females>Males.  It is a benign non encapsulated but extremely vascular ,slow growing and locally invasive tumours.  Microscopically it shows sheets of epithelial cells with large nuclei and granular
  • 6. Two types of glomus tumours: 1)Glomus jugulare: They arise from dome of jugular bulb, invade hypotympanum and jugular foramen , causing neurological sign of IX th to XII th cranial nerve involvement . They may compress or invade lumen of jugular vein. 2)Glomus Tympanicum: They arise from promontory of middle ear.
  • 7.
  • 8. CLINICAL FEATURES:  A)When tumour is intratympanic: • Earliest symptoms are deafness and tinnitus.Deafness is conductive type and tinnitus is pulsatile. • Otoscopy show red reflex through intact TM. “Rising sun”appearance is seen. • “Pulsation sign”(Brown’s sign) is positive. B) When tumour present as polyp: profuse bleeding from ear either spontaneously or after cleaning. • Dizziness or vertigo and facial paralysis may appear . Earache less common otorrhoea due to secondary infection.Examionation reveals red vascular polyp.
  • 9.
  • 10.  Cranial nerve palsies: It is a late feature .IX th to XII cranial nerves may be involved.dysphagia , hoarsness with unilateral paralysis of soft palate, pharynx and vocal cord.  Tumours may present as mass over mastoid or in nasopharynx.  Audible bruit over mastoid.  Some glomus tumours secrete catecholamines and produce their symptoms.
  • 11. DIAGNOSIS: 1)CT scan head 2)MRI 3)Four vessel angiography TREATMENT:  Surgical removal  Radiation  Embolisation  Combination of the above techniques
  • 12. CARCINOMA OF MIDDLE EAR AND MASTOID AETIOLOGY: Age- 40 to 60, females>males, chronic irritation may be the cause. PATHOLOGY: Tumour may arise primarily from middle ear or be an extension of carcinoma of deep meatus. Squamous cell variety is most common.
  • 13. CLINICAL FEATURES:  CHRONIC FOUL SMELLING DISCHARGE SPECIALLY BLOOD STAINED.  PAIN USUALLY SEVER AND COMES AT NIGHT  FACIAL PALSY  FRIABLE HAEMORRHAGIC GRANULATIONS OR POLYP  APPEARANCE OF OR INCREASE IN DEAFNESS OR VERTIGO.
  • 14. DIAGNOSIS  DEFINITIVE DIAGNOSIS IS MADE ONLY ON BIOPSY  EXTENT OF DISEASE IS JUDGED BY CLINICAL AND RADIOLOGICAL EXMINATION.  CT SCAN & ANGIOGRAPHY ARE USEFUL IN THE ASSESSMENT OF DISEASE.
  • 15. TREATMENT:  Combination of surgery and radiotherapy gives better results.