DISEASES OF THE EXTERNAL EAR 1.2 (AB) Flashcards

1
Q

What are exostoses?

A

“Benign bony outgrowths in the periosteum.”

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2
Q

What is the typical structure of exostoses?

A

“They demonstrate concentric lamellar bony organization.”

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3
Q

What are common symptoms of exostoses?

A

“Often asymptomatic but may cause conductive hearing loss if obstructive.”

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4
Q

What complications can arise from untreated exostoses?

A

“Infection and otalgia.”

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5
Q

What is the treatment for symptomatic exostoses?

A

“Excision using a diamond burr.”

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6
Q

What severe complication can arise from exostoses?

A

“Potential perforation of the tympanic membrane.”

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7
Q

What is squamous cell carcinoma (SCC)?

A

“A malignant tumor that can arise from the epithelium and adnexa.”

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8
Q

What percentage of external auditory canal tumors are SCC?

A

“20%.”

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9
Q

What is the second most common skin cancer?

A

“Squamous cell carcinoma.”

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10
Q

What percentage of malignant tumors of the auricle and EAC are SCC?

A

“80%.”

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11
Q

Does SCC commonly metastasize?

A

“No. metastasis is uncommon.”

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12
Q

What is the treatment for small SCC tumors?

A

“Local wide excision.”

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13
Q

What is the treatment for large SCC tumors?

A

“Whole auricle is sacrificed.”

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14
Q

What is the treatment for SCC with lymph node involvement?

A

“Radical en bloc resection.”

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15
Q

What is a major etiological factor for SCC?

A

“Excessive UV exposure.e.g.sunbathing.”

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16
Q

What is basal cell carcinoma (BCC)?

A

“A malignancy caused by the proliferation of basal cells in the epithelium.”

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17
Q

How does BCC compare to SCC in terms of aggression?

A

“BCC is locally aggressive and more invasive than SCC.”

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18
Q

Does BCC metastasize?

A

“No. but it is locally aggressive and can invade cartilage and bone.”

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19
Q

What is the primary risk factor for BCC?

A

“Overexposure to sunlight. particularly in outdoor workers.”

20
Q

How fast can a small BCC nodule grow?

A

“It can double in size within a week and become a large necrotic mass in a year.”

21
Q

What is the treatment for BCC?

A

“Wide surgical excision similar to SCC.”

22
Q

What is a malignant melanoma?

A

“An extremely rare malignancy developing from a pigmented nevus.”

23
Q

What are signs of malignant melanoma?

A

“Sudden elevation. ulceration and bleeding of a darkly pigmented nevus.”

24
Q

What is the treatment for malignant melanoma?

A

“Wide excision.”

25
Q

What is adenoid cystic carcinoma?

A

“A malignancy arising from ceruminous glands. also called cylindroma.”

26
Q

What are the clinical features of adenoid cystic carcinoma?

A

“Yellowish smooth masses with numerous dilated vessels.”

27
Q

What is the primary treatment for adenoid cystic carcinoma?

A

“Surgical excision.”

28
Q

What is an adenoma?

A

“A rare tumor originating from sebaceous glands in the fibrocartilaginous EAC.”

29
Q

What are the symptoms of an adenoma?

A

“Small. soft. painful swelling at the meatal entrance.”

30
Q

When does an adenoma become symptomatic?

A

“When it grows large enough to cause obstruction.”

31
Q

What is the treatment for adenoma?

A

“Complete excision with electrocautery of the tumor bed.”

32
Q

What is aural atresia?

A

“A congenital absence or severe narrowing of the external auditory canal (EAC).”

33
Q

How common is aural atresia?

A

“Occurs in 1 in 10 000 live births.”

34
Q

What embryonic structures are involved in aural atresia?

A

“1st and 2nd branchial arches and 1st branchial cleft.”

35
Q

How often is aural atresia bilateral?

A

“One-third of cases are bilateral.”

36
Q

What complication can EAC stenosis lead to?

A

“Canal cholesteatoma.”

37
Q

What are Group I external ear anomalies?

A

“Minor malformations with a mostly normal auricle and occasional EAC hypoplasia.”

38
Q

What are Group II external ear anomalies?

A

“Moderate malformations like microtia and EAC hypoplasia or aplasia.”

39
Q

What are Group III external ear anomalies?

A

“Severe malformations. including absent auricle and ossicles.”

40
Q

What are first branchial cleft anomalies?

A

“Congenital anomalies due to failure of normal obliteration of the first branchial cleft.”

41
Q

What types of abnormalities can first branchial cleft anomalies present as?

A

“Cysts. sinuses or fistulas.”

42
Q

What is Type I first branchial cleft anomaly?

A

“A duplication of the membranous EAC from ectoderm of the 1st branchial cleft.”

43
Q

What is Type II first branchial cleft anomaly?

A

“Contains ectoderm and mesoderm elements from the 1st and 2nd branchial arches.”

44
Q

Where are Type II first branchial cleft anomalies typically located?

A

“Anterolateral neck. anterior to the SCM. often coursing over the mandible and through the parotid.”

45
Q

What is the common presentation of first branchial cleft anomalies?

A

“Asymptomatic until infection occurs.”

46
Q

What is the treatment for recurrent first branchial cleft anomalies?

A

“Complete surgical excision with facial nerve preservation.”