Head and Neck Development Disorders Flashcards
what do orofacial clefts result from
disturbances in growth of face and oral cavity
what is cleft lip
defective fusion with the medial nasal process and maxillary process
what is cleft palate
failure of palatal shelves to fuse
what is the prevalance of cases in orofacial clefts
- CL and CP: 45% of cases
- CP: 30% of cases
- CL: 25% of cases
what population are orofacial clefts most common in
native americans and asians
what are the causes and risk factors of orofacial clefts
- genetic factors, syndromic
- environmental factors
- maternal alcohol and tobacco
- anticonvulsant therapy - phenytoin 10x risk
what is the possible prevention of orofacial clefts
folic acid in prenantal vitamins
what are the clinical features of orofacial celfts
-complete CL: extends upwards into nostril
- incomplete CL: does not involve the nose
- CP: may involve hard and soft palate
- minimal manifestation: bifid uvula
- may interfere with teeth development
how can orofacial clefts interfere with teeth development
- hypodontia
- malformed teeth
- bony defects
- malocclusion `
what is the treatment for orofacial celfts
- multidisciplianry approach
-surgical treatment - prosthetic appliances
is there tx indicated for bifid uvula
no
what are paramedian lip pits
congenital invaginations of the lower lip
- autosomal dominant inheritance
what are the clinical features and tx of paramedian lip pits
- bilateral and symmetrical fistulas on either side of midline of lower lip
- subtle depression or prominent buldge
- tx: none except for cosmetic reasons
what is Van der Woude syndrome
lip pits with CL and/or CP
- most common form of syndromic clefting
what are fordyce granules
ectopic sebaceous glands in oral mucosa
what are the clinical features and tx of fordyce granules
- multiple yellow or yellow-white papules
- buccal mucosa, vermillion of upper lip, retromolar pad, tonsillar area
- tx: none
do fordyce granules require biopsy
no
what feature is necessary in histopath to identify fordyce granules
sebaceous lobules
what is the cause of leukoedema
unknown
what are the clinical feautres and tx of leukoedema
- diffuse, gray-white color
- folded, wrinkled mucosa
- bilateral buccal mucosa
- white appearance disappears when mucosa is stretched
-tx: none
what is the differential dx for leukoedema and how do you rule out
- lichen planus
- leukoplakia
-candidiasis - all ruled out when mucosa is stretched
is microglossia common
no
what are the clinical features and tx of microglossia
- abnormally small tongue
- may be associated with a syndrome
- tx: depends on nature and severity. surgery and ortho
what is macroglossia
- enlargement of tongue
- more common than microglossia
what are the congenital causes of macroglossia
- vascular malformations
- lymphangioma
- hemihyperlasia
- down syndrome
what are the acquired causes of macroglossia
- edentulous patients
- amyloidosis
- myxedema
what is ankyloglossia - tongue tie
developmental anomaly of the tongue
what are the clinical features and tx of ankyloglossia
- short, thick frenum
- may result in speech defects
- may result in breast feeding difficulties
- tx: frenectomy for functional problems
what is the lingual thyroid
normally the thyroid descends into neck anterior to trachea
- when the primitive gland does not descend normally, ectopic thyroid tissue may be found between foramen cecum and epiglottis
what are the clinical features of lingual thyroid
- Most common in females (4x) due to hormonal influences
- ectopic gland (70%) is often only thryoid tissue
- range in size: small, asymptomatic, large lesions may block airway and cause dysphagia or dyspnea
- hypothyroidism in 33%
how is lingual thyroid dx
- thyroid scan
- avoid excisional biopsy because may be patients only thyroid tissue
what is the tx for lingual thyroid
-periodic follow uo
- thyroid hormone replacement
how is lingual thyroid determined in biopsy
if there is iodine present
describe fissured tongue
often hereditary, may also be degenerative process