Mouth and Throat Disorder Flashcards

1
Q

A 19-year-old man comes to your office with a complaint of a sore throat. His illness began 3 days ago with a sore throat, followed by persistent fevers of 102 0F.
What are the common diagnostic considerations for patients with acute sore throat?
What questions are helpful in determining the cause of sore throat? OLDCART
How do you assess for the presence of potentially serious causes of sore throat? (DDx)

A

-diff dx- strep, mono, pharyngitis, post nasal drip,

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2
Q

most common cause of sore throat

A

viral
-common for young children

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3
Q

acute tonsillitis and pharyngitis

A

-Acute viral or bacterial infection
-Viral most common -> ibuprofen, aspirin, decongestant (caution for young children)
-Tonsillitis and pharyngitis typically occur simultaneously -> pharyngitis precedes tonsilitis usually*
-Peak incidence in winter and early spring
-Repeat attacks
-schools, cramped living, traveling, or working conditions, Military camps commonly affected
-M=F
-All ages are affected (MC 5-15 yoa)
-Tonsillitis under 3 years -> rare and usually viral

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4
Q

acute tonsillitis and pharyngitis etiology

A

-Common causes- Influenza A and B viruses, H1N1 influenza, Respiratory syncytial virus (RSV), Adenovirus
-Rare causes- Herpes simplex, Neisseria gonorrhoeae

-serious causes:
-Streptococcus group A* and G, group A beta-hemolytic streptococci
-Fusobacterium necrophorum*
-Epstein-Barr virus
-Staphylococcus aureus
-Neisseria gonorrhoeae*
-Chlamydia pneumoniae
-Mycoplasma pneumoniae
-Chlamydial trachomatis*
-other causes: GERD, Postnasal drainage from chronic allergies, Neoplasm, Corynebacterium diphtheriae

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5
Q

pharyngitis signs and symptoms

A

-Fever, Sore throat, Halitosis, Dysphagia, Odynophagia, Cervical lymph nodes, Headache, Otalgia, Lethargy/ malaise, Vomiting,
-Difficulty breathing-> Mouth breathing, snoring, nocturnal breathing pauses, or sleep apnea
-Swollen hyperemic red tonsils / pharynx
-Often coated with a yellow or thin white non-confluent membrane
-Peels away without bleeding* (different from diphtheria)*
-Throat may be edematous, blistered, or have painful ulcers
-CHRONIC tonsillitis- White particulate matter in tonsillar crypts (pockets) **
-Cervical lymph nodes may be swollen, enlarged, or tender
-Dry mucous membranes- mouth breathers

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6
Q

GABHS pharyngitis(group A beta hemolytic streptococcus)

A

-Often associated with:
-Headache
-Pharyngeal exudate
-Painful cervical adenopathy
-GI symptoms
-Chills
-High fever
-Hoarseness, coryza and cough NOT associated**

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7
Q

Viral pharyngitis

A

-usually associated with:
-sneezing
-rhinorrhea
-cough!

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8
Q

GABHS pharyngitis predisposing factors

A

-GABHS epidemics
-Recent family history - may be passed between family members ; ‘ping-pong’ effect
-Close quarters (military barracks, dormitories)
-Immunosuppression
-Recent illness
-Also ask about previous treatments, treatment failures, and medication allergies
-consider antibiotics to prevent spread (even if pt is fine)

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9
Q

GABHS differential diagnosis

A

-Mononucleosis
-Peritonsillar abscess
-Parapharyngeal abscess- can comprise airway
-Scarlet fever- sandpaper rash
-Diphtheria –gray pseudomembrane -> cannot come off -> bleed, antitoxin -> cause heart valve problems
-Epiglottitis
-Vincent’s Angina (Trench mouth)- can cause lugwigs angina (deep cellulitis of neck)
-Squamous cell carcinoma of the tonsils

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10
Q

Rule out or Rule in Group A streptococcal pharyngitis

A

-Suspected on the basis of clinical signs and symptoms
-Confirmed with laboratory testing – d/o how likely it is to be GABS
-Positive rapid antigen test or a positive throat culture (days for results)
-A negative rapid antigen test does NOT rule out streptococcal pharyngitis and should be confirmed with a throat culture **
-White blood count (WBC) with differential
-Monospot - if multiple cervical lymph nodes swollen
-Lateral neck radiograph - to rule out epiglottitis
-Computed tomography (CT) scan - to rule out pharyngeal abscess

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11
Q

centor criteria

A

-Group A beta-hemolytic streptococcal infections –
risk of Rheumatic fever and Glomerulonephritis
-The following may indicate streptococcal infections in the absence of throat culture results
-1. Fever >100°F (38°C)
-2. Pharyngotonsillar exudates
-3. Tender anterior cervical adenopathy
-4. Lack of a cough

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12
Q

GABHS treatment

A

-supportive care
-relieve fever, sore throat, tonsillar swelling
-gargle with warm salt water
-drink warm fluids
-start antibiotics?
-pts with zero or one centor criteria -> very low risk -> do not need throat cultures or RADT of throat swab and should not receive antibiotics
-2. pts with 2-3 centor criteria -> need throat cultures AND RADT of throat swabs since + result would warrant antibiotic treatment -> ALWAYS SEND CULTURE
-3. pts who have all 4 centor criteria are likely to have GABHS -> receive empiric therapy without throat culture or RADT
- + COUGH- NOT STREP

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13
Q

GABHS antibiotics

A

-Antibiotics recommended when GABHS confirmed with rapid antigen-detection test or throat swab culture
-RF can be prevented if treatment given up to 9 days of presentation
-Ensure follow-up for recurrent infections lasting over 3 weeks
-Prevent future attacks
-Prevent spread -> ask pt not to go to work for up to 3 days
-PCN treatment of choice in both children and adults
-adults:
-1st choice- Pen VK 250mg BID or 500mg TID x 10 days
-amoxicillin 500mg Q 12h x 10 days also reasonable
-single dose IM benzathine/procaine penicillin- can be given as single dose, drug is expensive, frequently unavailable, causes injection site pain
-secondary options:
-azithromycin, clarithromycin, erythromycin base, cephalexin (cefadroxil, clindamycin)

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14
Q

rheumatic fever

A

-immune complex
-complexes placed on the valves
-endocarditis
-prophylaxis penicillin for up to 5 years daily OR single dose IM benzathine/procane penicillin 1x month (painful, expensive) -> for pts that are not compliant

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15
Q

rheumatic fever jones criteria

A

-major criteria: carditis, arthritis, chorea, erythema marginatum, subcutaneous nodules
-minor criteria- high fever, joint pain (without inflammation) -> arthalgia, ESR, CRP, prolonged PR interval in ECG
-fleeting arthritis- one joint gets better and the next becomes inflamed
-2 major and 1 minor to dx
-throat swab culture or rapid strep
-elevated/increasing strep antibody titer

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16
Q

tonsillectomy or adenotonsillectomy treatment

A

-pts with recurrent tonsillitis or pts which all other treatments have failed
-Risk vs. benefit
-Absolute indications -> Upper airway obstruction, severe dysphagia, sleep disorders, or cardiopulmonary complications; Peri-tonsillar abscess OR Tonsillitis resulting in febrile convulsions
-Relative indications:
-3 or more tonsil infections per year
-Streptococcal carrier not responding to treatment
-CI: Bleeding diathesis; Poor anesthetic risk or comorbidities

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17
Q

other strep considerations

A

-What is the ‘Strep carrier state’?
-Some pts carry GABHSB but do not manifest illness-> never treated
-unknowingly infect family members, sometimes repeatedly
-If multiple family members show repeated illness -> worthwhile to perform throat cultures on the asymptomatic family members
-pregnancy- GABHS vaginal infection associated with increased risk of preterm delivery
-Eradication of beta-hemolytic streptococcus from nasopharynx is advised if infection occurs during pregnancy

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18
Q

non-suppurative complications of GAS

A

-NO PUS
-Rheumatic fever
-Rheumatic heart disease
-Acute Glomerulonephritis- hematuria, high BP, edema

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19
Q

other ways strep can present

A

-scarlet fever- sandpaper like rash
-impetigo - blisters around mouth

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20
Q

suppurative complications of GAS

A

-PUS +
-Peri-tonsillar abscess (quinsy)
-Impetigo
-Otitis media
-Mastoiditis
-Sinusitis
-Bacteremia
-Pneumonia
-Meningitis
-Osteomyelitis (OM)
-Necrotizing fasciitis
-Cellulitis

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21
Q

peritonsillar abscess dx

A

-History and clinical findings
-CBC with diff
-Blood cultures
-Monospot test
-Tonsillar swab

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22
Q

peritonsillar abscess symptoms and signs

A

-Unilateral ±, severe throat pain
-Dysphagia
-Odynophagia
-Trismus (difficulty opening the -mouth wide)
-Neck pain
-Referred ear pain
-Drooling -> also seen in epiglottitis
-Muffled (‘hot potato’) voice- muffled mumbling
-Fever
-Severe dehydration
-Possibly extreme distress
-Tonsillar hypertrophy
-Palatal edema
-CONTRALATERAL deflection of the swollen uvula -> spreads laterally*
-trouble breathing
-Inferior and MEDIAL displacement of the infected tonsil
-Fluctuant peritonsillar fullness
-Tender cervical adenopathy
-Edema in the neck due to infective lymphadenopathy
-Inflamed oropharyngeal mucosa
-Drooling
-Rancid breath
-Brawny pitting of the ipsilateral neck in advanced infection
-Signs and symptoms may not always be dramatic

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23
Q

peritonsillar abscess

A

-collection of fluid in peritonsillar space -> pushes tonsil medially, -> obscure definition of anterior tonsillar pillar
-Beware of examining oropharynx in children-> use of tongue depressor in airway obstruction may provoke respiratory arrest
-Maintain a high index of suspicion
-Treatment of peritonsillar cellulitis - either resolves over several days or evolves into peritonsillar abscess
-AKA Quinsy
-One or both tonsils affected -> form pus pockets
-Onset of symptoms to abscess formation approx. 2-8 days
-may form without preceding hx of tonsillitis

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24
Q

retropharyngeal abscess

A

-Presentation depends on stage of illness
-Early in disease- indistinguishable from uncomplicated pharyngitis
-With disease progression- symptoms related to inflammation and obstruction of the upper aerodigestive tract develop
-SERIOUS

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25
Q

retropharyngeal abscess signs and symptoms

A

-Dysphagia
-Odynophagia
-Drooling with decreased oral intake
-Neck stiffness
-Muffled, or with a “hot potato” quality
-Respiratory distress (stridor, tachypnea, or both)
-Neck swelling, mass, or lymphadenopathy
-Trismus
-Chest pain (in patients with mediastinal extension)- can spread

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26
Q

retropharyngeal abscess management

A

-Incision and drainage and/or needle aspiration
-caution Internal carotid artery!- lateral to the medial plane of the ramus of the mandible
-Drainage of the abscess (in adults – local anesthesia) -> obstruction
-Antibiotic coverage
-Close monitoring
-Oral rehydration
-Tonsillectomy – with hx or frequent previous tonsillar infections -> After infection has resolved

27
Q

mononucleosis

A

-classic triad- lymphadenopathy, fever, sore throat, + or - exudates
-Malaise/fatigue*, splenomegaly, pharyngeal petechiae and occasionally a maculopapular rash

28
Q

mononucleosis workup

A

-Relative and absolute lymphocytosis
-Atypical lymphocytes present**
-IgM antibodies
-Positive heterophile agglutination test (Monospot test)
-Specific serology for Epstein-Barr virus

29
Q

mononucleosis treatment

A

-Supportive care; prednisone
-Ampicillin may cause rash
-Acute course is prolonged, lasting up to 4 weeks, with full recovery taking several months
-Avoid contact sports — splenic rupture**

30
Q

oral candidiasis

A

-Spectrum of opportunistic infective disorders
-Caused by a yeast (Candida spp.)
-Most commonly C. albicans
-Involving the skin and/or mucous membranes
-Stomatitis (oral thrush) in neonates, children, and elderly -> inflammation/ulcers affects outside of mouth
-Most commonly seen at extremes of age
-vaginal candidiasis very common with antibiotic use -> hx -> treat both at same time

31
Q

candidiasis risk factors

A

-Broad-spectrum antibiotics
-Chronic use of inhaled and oral corticosteroid -> gargle water after
-Hormonal factors (including birth control pills)
-Diabetes
-Malignancy
-HIV/AIDS (esophageal)

32
Q

candidiasis S&S and dx

A

-In mild disease - asymptomatic
-Sore throat, odynophagia
-Cheesy, raised white plaques
-Can be wiped off, revealing a raw, erythematous, and sometimes bleeding base
-Thick dark brownish coating, deep fissures
-Pain/discomfort on eating and drinking -> Especially spicy or acidic food and drink
-Angular cheilosis is common -> outside mouth ulcers
-Diagnosis – clinical; wet mount -> reveals hyphae

33
Q

management candidiasis management

A

-Mild manifestation-Topical nystatin or clotrimazole
-Systemic therapy:
-Immunosuppressed pts., or moderate-to-severe disease, refractory or recurrent disease, or esophageal involvement (e.g. fungal esophagitis)
-Treatment of choice: Oral fluconazole or itraconazole solution
-Recurrent or severe mucocutaneous candidiasis-> should prompt investigation into predisposing causes

34
Q

acute necrotizing gingivitis (ANUG)

A

-Acute infection of the gingiva with organisms such as -> Prevotella intermedia, Alpha-hemolytic streptococci, Actinomyces species
-Painful acute gingival inflammation and necrosis, often with bleeding, halitosis, fever, and cervical lymphadenopathy
-ulcerative
-Vincent’s Angina - trench mouth
-Accelerated destruction of affected tissues & local or systemic spread of infection
->Coronary artery disease (CAD); CVA (bacteria sits on the valves!)
->Periodontal disease in pregnancy - increase in preterm birth

35
Q

ANUG treatment

A

-Debridement and IV Antibiotics
-Penicillin plus Metronidazole, with clindamycin
-Erythromycin alone as an alternative
-Antiseptic [Chlorhexidine mouth wash] and analgesics
-clean out the area

36
Q

ludwigs angina

A

-MC deep neck infection
-can arise from any infection
-Rapidly progressive, potentially fulminant cellulitis
-Most commonly encountered neck space infection
-Cellulitis of the sublingual and submaxillary spaces
-History - typically originates from an infected or recently extracted tooth
-Most common site - lower second and third molars
-edema -> fluid collects -> obstruction of airway by tongue -> possible tracheostomy due to inability to intubate (tongue in way)

37
Q

ludwigs angina management

A

-PRESERVE AIRWAY - Intubation (early) or tracheostomy***
-Asphyxiation - most common cause of death
-Monitor patients closely and treat promptly with intravenous antibiotics
-Ampicillin-sulbactamOR
-Penicillin G plusmetronidazole OR
-Clindamycin

38
Q

leukoplakia

A

A white lesion that cannot be removed by rubbing the mucosal surface
-precancerous
-bx

39
Q

erythroplakia

A

Similar to leukoplakia except that it has a definite erythematous (red) component

40
Q

oral lichen planus

A

Most commonly presents as lacy leukoplakia but may be erosive; definitive diagnosis requires biopsy.

41
Q

oral cancer

A

Early lesions appear as leukoplakia or erythroplakia
More advanced lesions will be larger, with invasion into tongue such that a mass lesion is palpable.
-Ulceration may be present**
-pipe smokers
-HPV
-any constant irritations- tooth -> changes mucosa membrane -> precancerous
-squamous cell carcinoma- ulcer depression -> tend to spread

42
Q

oral leukoplakia

A

-Predominantly white lesion of the oral mucosa
-Cannot be characterized clinically or pathologically as any other defined lesion -> Leukoplakia is a diagnosis by exclusion**
-you usually think other things first like thrush
-Requires confirmation by bx -> crucial aspect of clinical management
-Homogeneous or heterogeneous plaques
-verrucous lesions
-Erythroplakia (speckled leukoplakia)
-most important risk factor for these lesions is tobacco use

43
Q

oral leukoplakia benign vs malignant

A

-diagnosis of exclusion
-Benign Vs. Malignant:
-Some simple leukoplakias -> benign lesions
-Many are squamous carcinoma***:
-Many leukoplakias in the floor of the mouth
-All erythroplakias - regarded as premalignant
-hair leukoplakia- usually on sides
-palpating- may be firm, deep, hard

44
Q

oral leukoplakia management

A

-removal of any contributing factors
-May involve antifungal treatment and corrective dental
-More aggressive management may involve surgical removal
-Lesion recurrence and/or progression to carcinoma is common
-radiation
-removal of local lymph nodes

45
Q

glossitis, glossodynia, burning mouth syndrome

A

-glossitis- inflammation of tongue, red, no pain often
-can be due to malnutrition, dehydration (diabetics), autoimmune
-glossodynia- glossitis with pain
-no inflammation- chronic burning mouth sensation -> spicy food aggravate

46
Q

aphthous ulcers

A

-Etiology – unknown
-Human herpesvirus 6
-Nonkeratinized mucosa affected- mucosa membrane
-Single/multiple
-Recurrent
-Painful, small round ulcerations
-Yellow-gray fibrinoid centers surrounded by red halos
-Pain – 7-10 days
-Complete resolution – 1-3 weeks
-malnutrition, immunosuppressed, stress!

47
Q

aphthous ulcers treatment

A

-Non-specific
-Topical steroids
-Analgesics
-Magic Mouthwash
-Equal parts of Diphenhydramine 12.5 mg/5 mL, Viscous lidocaine 2%, and Maalox 1 part
-Swish and swallow Every (q) 4 – 6 hours
-If diagnosis unclear, persistent ulcers – biopsy

48
Q

epiglottis

A

-Leaf-shaped cartilaginous structure covered with a mucous membrane
-Located at base of the tongue and covers the larynx during swallowing
-Acute inflammation of the epiglottis, aryepiglottic folds and the arytenoid soft tissue
-Epiglottis – most common site of swelling; upper airway obstruction – ‘supraglottitis’ (above)***
-croup is below epiglottis
-TRUE EMERGENCY

49
Q

pediatric epiglottitis

A

-Drooling (80%)**
-Dysphagia
-Distress
-Fever
-Seriously ill and apprehensive
-Hot potato voice**
-Stridor- cant breathe
-“Sniffing position”- neck extension to help breathing
-Hypoxia
-Cyanosis – grave sign
-Cough - rare
-Appear toxic

50
Q

adult epiglottitis

A

-Preceding URI
-Rapidly developing sore throat (95%)**
-Muffled voice (hot potato voice)
-Odynophagia - out of proportion to physical findings
-Dysphagia
-Tripod position- trouble breathing
-Sever pain on palpation of larynx
-Irritability
-Tachycardia
-Adults – less acute -> longer neck

51
Q

epiglottitis management

A

-Hospitalization
-Evaluate ABC’s
-Secure airway
-Intubation and cricothyrotomy tray - at the bedside if you have to -> OR if you can
-Continuous monitoring
-Supplemental oxygen - blow-by oxygen – if tolerated
-IV placement only after airway secured
-NPO
-Transfer to ICU – prn – after airway secured
-ENT and anesthesiology consult
-IV antibiotics- Empiric coverage – Ceftriaxone or Cefuroxime -> switch to oral to complete a course for 10 days
-White patches – candidiasis
S/P trauma – S. aureus
-Dexamethasone → IV bolus; then infusion -> taper steroids; oral antibiotics
-<10% adults require intubation

52
Q

epiglottitis labs

A

-Nonspecific
-Once airway secured – can be obtained
-WBC count > 15,000-45,000 cells/mm3 with a predominance of bands
-Blood culture results may show Hib in 12-90% of cases
-Epiglottic cultures obtained during endotracheal intubation are positive in half of cases

53
Q

epiglottitis imaging

A

0Never obtain a lateral neck radiograph before achieving definitive airway control
-Radiography – to confirm diagnosis and to exclude other causes
-Lateral soft tissue x-ray of neck:*
-reveals a swollen epiglottis (i.e., thumbprint sign)

-thickened aryepiglottic folds
-dilation of the hypopharynx
-Negative radiograph does not rule out diagnosis

54
Q

CT epiglottitis

A

-adult with acute epiglottitis -> column of air around the epiglottis
-right side is more swollen than the left, and the hypoattenuating area is suggestive of fluid or an early abscess formation

55
Q

laryngoscopy epiglottitis

A

-never perform on a child unless expert in pediatric intubation
-adults are less acute BUT always be prepared
-intubation and cricothyrotomy tray by bedside

56
Q

prophylaxis epiglottitis

A

-Hib vaccine
-@ 2, 4, 6 months -> final dose given at > or equal to 12 months (dont need to know)
-epiglottitis can still occur with complete vaccination
-rifampin prophylaxis for contacts with no vaccination or with increased risk

57
Q

croup

A

-Acute
-Stridor; shortness of breath; cough
-Progressive shortness of breath, may progress to severe respiratory distress
-Precipitating factors: Antecedent URI
-Clinical course: Symptoms may plateau or progress to respiratory distress; not as toxic; overall, self-limited
-X-ray: Steeple sign in subglottis* (narrowing below epiglottis on plain films of the neck

58
Q

croup S&S

A

-Prodrome of fever and URTI
-Rhinorrhea; Cough; Low-grade fever
-Typically, between 6am and 6pm
-Appears nontoxic (common); -Fatigue; tachycardia; tachypnea
-Restless (common)-> prefers sitting upright in a parent’s lap
-Absence of drooling
-morning **
-Normal voice or laryngitis (Hoarseness )
-Seal-like barking cough,* gasping
-Inspiratory stridor
-Retractions of the accessory chest muscles
-No change in stridor with positioning
-Nontender larynx*
-Worsening disease and possible impending respiratory failure:
-Change in mental status (eg, fatigue, listlessness, restlessness)
-Increased retractions
-Decreased breath sounds with decreasing stridor
-Pallor or Cyanosis

59
Q

croup tests

A

-Diagnosis – clinical
-Lab tests – non-specific; may show viral illness – increased WBC’s
-Plain films:
-To confirm the diagnosis BUT only if airway is secure
-Exclude other disorders – FB; epiglottitis; bacterial tracheitis, or retropharyngeal abscess
-PA view - steeple sign (subglottic narrowing)
-Lateral view – distended hypopharynx

60
Q

croup treatment

A

-simple- reassurance/education, cool mist (may loosen secretions), oxygen, frequent monitoring, hydration
-mild-moderate- glucocorticoids, dexamethasone, prednisone, budesonide
-mod-severe- nebulized epinephrine observe 3-4 hrs, d/c steroids, antibiotics

61
Q

angioedema

A

-Acute
-M=F
-Itching, swelling, transitory, light-colored, edematous plaques
-Location: Any area, particularly lips, eyelids, genitals, tongue, larynx possible
-Precipitating factors: Medication, foods, insect bites
-Management: Antihistamines; steroids

62
Q

other diseases of larynx

A

-Dysphonia
-Hoarseness- follow up on!**
-Stridor
-Laryngopharyngeal reflux
-Masses of the Larynx
-Vocal fold polyps, cysts, paralysis
-Squamous cell carcinoma of larynx
-FB inhalation and ingestion

63
Q

laryngeal disease

A

-primary symptoms:
-1. Hoarseness:
-Abnormal vibration of the vocal folds
-voice is breathy when too much air passes incompletely apposed vocal folds, as in unilateral vocal fold paralysis or vocal fold mass
-2. Stridor
-Above the vocal folds - inspiratory stridor
-Below the vocal fold - expiratory or biphasic stridor
-timing and rapidity of onset critically important

64
Q

laryngitis

A

-Acute or chronic inflammation: erythema & edema of laryngeal mucous membranes
-1. Acute
-Due to URTI - viral infections (evident by cough and coryza)
-Voice abuse (yelling, talking, singing)
-Resolve spontaneously with voice rest and humidification
-2. Chronic:
-Exposure to irritants (cigarette smoke, alcohol, gastric contents)
-Benign lesions of laryngeal structures
-Hoarseness of voice or a harsh voice with a deep pitch is often the main symptom
-Direct laryngoscopy - diffuse laryngeal erythema and edema, vascular engorgement of the vocal folds