Congenital Nasal Anomalies Flashcards

1
Q

How do you classify congenital Nasal anomalies?

A

Bartlett/Whitaker

Type 1- Agenesis, Hypoplasia

Type 2- Duplication, Hyperplasia

Type 3 - Clefts

Type 4 - Neoplasms and Vascular anomalies

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2
Q

Which syndromes are associated with congenital nasal anomalies of ypoplastic/agenesis type?

A
  1. Aperts (bilat narrowed bony vault, chonal atresia/stenosis)
  2. Binder (midface retusion, absent ANS, short nose, flat bridge)
  3. Fraser (crypopthalmia and nasal midline cleft, choanal atresia)
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3
Q

Describe the congenital anomalies of agenesis/hypoplasia

A

AGENESIS of parts

  • Arhinia (total no olfactory system)

HYPOPLASIA of parts

  • Nasal cavity atresia
    • choanal atresia = posterior outlet= insufficient excavation of nasal pits
    • pyriform aperture stenosis
  • Heminose
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4
Q

Describe your nasal reconstruction plan for Binder syndrome

A

Delay until bone maturation (adolescence)

1- orthodontics

2- orthognathic surgery: Lefort 1 or 2 with BG (given mdiface retusion and class 3)

3- nasal augmentation and tip projection

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5
Q

Describe congenital nasal anomalies of duplication/hyperplasia

A

DUPLICATION

  • Polyrhinia
  • Supernumerary nostrils

HYPERPLASIA

  • Proboscis lateralis (tubular fleshy apepndage attached with MCT) 2’ to anomaly of LNP
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6
Q

Which Tessier facial clefts are associated with nasal congenital anomalies?

A

0-14

1-13

2-12

3-11

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7
Q

Which tessier cleft with nasal anomaly is most common

A

TEssier 0-14

= FrontoNasal Dysplasia

cleft of central midface

bifid nasal tip, orbital hypertelorism

frontonasal encephalocele

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8
Q

Define an encephalocele

A

Herniation of crnial contents through bony defect in skull

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9
Q

How do you classify Fontonasal Encephaloceles?

A
  1. Naso frontal : encephalocele between frontal and nasal bones
  2. Nasoehtmoidal: encephalocele between nasal bones and cartilages
  3. Naso-orbital: encephalocele between medial orbital walls
  4. Combined
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10
Q

Where are encaphaloceles located

A
  • occipital - most common
  • frontal
  • parietal
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11
Q

What are clinical signs of an encephalocele

A

Location of mass (occipital, parietal, frontonasal)

trasnilluminates

pulsatile

blueish

compressible, expands with valsalva

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12
Q

What is the prognosis of encephalocele

A

high mortality (50% survive w occipital lesion)

hihgh mornity (50% with neurodeficit)

Best prognosis if anterior lesion, pure meningocele

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13
Q

What is the management of frontoehtmoidal encephalocele

A

Multidisciplinary with NSx

  • need tight dural seal
  • goals to remove mass, repair bone defect after dural repair, reconstruct medial orbital walls
  • frontal craniotomy, rotate segments downward medially and posteriorly to correct trigonocephaly, hypertelorism
  • Nasal recon with costochondral graft
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14
Q

What is your DDX for a congenital nasal mass?

A

BENIGN

  • Dermoid
  • Glioma
  • Hairy nevus
  • Encephalocele
  • Neurofibroma
  • Pilomatrixoma
  • Mesenchymal tumor (lymphagioma, angiofibroma, lipoma, hemangioma)
  • polyp
  • sinus tract (nasolacrimal duct cyst)

MALIGNANT

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15
Q

What is a nasal glioma

A

Heterotopic growth of neural tissue 2/ deficient regression of neural tissue +/- connection with dura

= sequestrated encephalocele

Most extranasal (60%), some intranasal (30%) or both (10%)

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16
Q

What are clinical signs of a nasal glioma

A

Firm non compressible,reddish

no transillumination

no enlargement with compresion of IJV (Furstenberg sign)

17
Q

How do you investigate a nasal mass you suspect is a nasal glioma

A

CT and MRI to check for intracranial extension

18
Q

How do you manage a nasal glioma

A

Multidisciplinary

Extranasal glioma: with no intracraial extesnion, lateral rhinotomy, external rhiploasty, midline nasal, coronal

If intrancranial component - need both intracranial and extracrnail approaches

Recurrence 5%

19
Q

What is a nasal dermoid

A

Hamartoma; abnormal growth of skin apepndages in epithelial lined cavity or sinus

Most common congenital nasal anomaly

20
Q

What are clinical signs

A

non compresisble, no trasnillumination, negative furstenberg

MIdline mass along columella, dorsum, nasoglabellar region

*sinus opening or punctum pathognomonic

21
Q

WHat is the etiology of nsal dermoid

A

Failure of separation of neruoectodermal and ectoderm tissue

  • failure of dura to regress and forms sinus cavity
  • persistence of dura wihtin cartilage layers

entraped epithelium within fused MNP

22
Q

How do you investigate a nasal mass that you suspect is a nasal dermoid

A
  1. First CT
  2. MRI if CT suggest intracrnial extension
23
Q

WHat do you treat nasal dermoid

A

no INTRACRANIAL EXTENSION

  • extracranial appraoch (open rhino approach, lateral rhinotomy

INTRACRANIAL

  • Nsx consult
  • frontal craniotomy
24
Q

Define nasal Hemangioma

A

vascular tumor of proliferating endothelial cells with no dysplastic vessels

25
Q

What is the clinical presentation of a nasal hemangioma?

A
  • appears in 1st wk of life
  • red/purple
  • rapid proliferation til 5-6yrs then involution over years
26
Q
A