Respiratory Infections Flashcards

1
Q

What is rhinitis

A

nasal turbinate swelling and congestion, nasal drainage which can be clear, yellow, green

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2
Q

What is sinusitis

A

inflammation of the sinus cavity with filling of the sinuses with mucous

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3
Q

What is pharyngitis

A

inflammation of the pharynx, with or without exudate

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4
Q

What is laryngitis

A

inflammation of the larynx/vocal cords, usually with changes in the voice or a characteristic barking cough.

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5
Q

Clinical features of upper respiratory infections

A
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6
Q

Clinical features of acute rhinosinusitis

A

Nasal congestion, purulent nasal discharge, facial pain or pressure are all seen. Fever only lasts a few days in viral disease, but the other symptoms cough, nasal drainage, sputum production, etc can last for almost 2 weeks in viral disease

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7
Q

Criteria for bacterial rhinosinusitis

A

Persistent > 10 days without improvement

Severe symptoms for 3-4 days

“Double-sickening” indicating bacterial superinfection after viral illness

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8
Q

Non-antibiotic treatment for rhinosinusitis

A

Saline irrigation “neti pot”

Intranasal glucocorticoids—decreases inflammation

Intranasal sympathomimetic decongestants (pseudoephedrine spray—use for max of 3 days only! Or will get “rhinitis medicamentosa”)

Oral sympathomimetic decongestants—relieve pressure in sinuses and nasal turbinate swelling through sympathomimetic effect

Antihistamines—help with itching and pain of nose, helps dry secretions

Mucolytics—thin mucus so it drains more easily from sinuses

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9
Q

NNT for rhinosinusitis

A

13 for adults

5 for children

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10
Q

Most common cause of pharyngitis in children

A

Group A beta-hemolytic Streptococcus (GAS)

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11
Q

Serious cause of pharyngitis that presents with intense pharyngitis, cervical lymphadenopathy and white/gray membranes that can occlude airways and cause death

A

Diphtheria due to Corynebacterium diphtheriae

Vaccine preventable

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12
Q

Clinical features of pharyngitis

A
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13
Q

Diagnostic testing performed for pharyngitis

A

Rapid streptococcal tests- sensitivity and specificity of up to 95%! Throat culture is done reflexively if negative. If suspect STI’s, need to test specifically for those with additional tests

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14
Q

Treatment for Group A Strep

A

1st generation Penicillin (IM or oral) as recommended primary treatment! Clinically, because it can be dosed less often, amoxicillin is used unless the patient refuses oral medications.

The main reason why GAS pharyngitis is always treated is that treatment lessens the risk of Rheumatic Fever happening as a complication to GAS infection

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15
Q

Presentation of Peritonsillar or parapharyngeal abscess

A

Infection and pus collection in the deep tissues of the pharynx around the tonsillar pillar. Presents with fever, very sore throat, and deviation of the uvula on examination as well as swelling behind or around the tonsil unilaterally. People may sound like they are speaking with a mouthful of hot food aka “hot-potato” voice, and may have pain with opening the jaw or refusal to open the mouth.

These are less dangerous compared to retropharyngeal abscesses, because they rarely cause concern for airway safety, and may nor may not require drainage in addition to IV antibiotics.

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16
Q

Presentation of retropharyngeal abscess

A

Infection and pus collection in the prevertebral spaces of the posterior pharynx. These also present with throat pain are intrisically dangerous and considered an airway emergency as they can rapidly enlarge, obstruct breathing, and make intubation impossible. They may be symmetric or asymmetric, and imaging is required to diagnose.

The retropharyngeal soft tissues should usually be minimally seen on a lateral film, any widening that is greater than the adjacent vertebral bodies is significant retropharyngeal edema indicating possible abscess.

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17
Q

Epiglottitis def and presentation

A

Inflammation of the epiglottis and adjacent supraglottic structures. This starts out as what looks like a routine cold or croup, but can progress to life-threatening airway obstruction as shown above when the usually thin, flexible epiglottis becomes edematous and woody, swelling to close off the airway completely. Pediatric patients may present in the “tripod” position, shown below, to try to open their airway and get more air, and will usually be drooling and very sick appearing, with breathing their sole focus.

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18
Q

Causes of epiglottitis

A

Haemophilus influenzae type b (Hib) is the most common infectious cause of epiglottitis in children and prevented with vaccine. Also, Staph Aureus can be seen as a cause, usually in kids with underlying varicella. In adults, epiglottitis has been associated with a broad range of bacteria, viruses, combined viral-bacterial infections, fungi, and noninfectious causes, and is a rare diagnosis.

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19
Q

Treatment for epiglottitis

A

Securing the airway with expert airway help from an anesthesiologist or critical care physician is the first priority and all other care is delayed until that occurs to prevent the child crying and occluding their airway irreversibly with IV placement orr other stimulation. Epiglottitis is always treated with broad spectrum antibiotics empirically due to its immediately life-threatening nature.

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20
Q

Laryngitis def and presentation

A

Commonly known as “I lost my voice.” Extremely common and self-limited, lasts less than 3 weeks. Clinical findings are hoarseness-to-total voice loss, associated with rhinorrhea, cough, and mild sore throat. Causes are mostly viral, but can also be caused by common pharyngeal flora: Moraxella catarrhalis, Hemophilus influenzae, and Streptococcus pneumoniae. Antibiotics not used empirically; if persistent voice changes, get ENT to see and scope to evaluate for tumor, GERD, functional problem, or unusual infection as cause.

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21
Q

What is laryngotracheitis

A

Croup

inflammation and infection of the upper airway, typically just below the vocal cords, also referred to as subglottic edema.

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22
Q

Presentation of croup

A

Children less than two are most symptomatic due to the small diameter of their airways. They will also have other typical cold symptoms, like runny nose and low grade fever.

Croup causes a characteristic “seal’s bark” cough and stridor

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23
Q

Imaging of croup

A

Croup is a clinical diagnosis most of the time, if there is doubt about the diagnosis, or respiratory distress due to another cause is in the differential diagnosis, a neck x-ray can be done to look for the characteristic subglottic narrowing associated with croup. There are a few neck x-rays findings to be familiar with after this lesson–this “steeple sign” of croup is one of them!

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24
Q

Croup treatment

A

Croup that causes stridor at rest should be treated with a one-time dose of oral steroids, to decrease the airway edema and prevent worsening respiratory distress. The illness usually lasts 3 or so days, and peaks on the evening of the second day, so using dexamethasone as a steroid that has a long half-life of about 24 hours is the usual choice. When patients are observed to have significant respiratory distress with tachypnea and retractions due to croup, they can temporarily benefit from a racemic epinephrine nebulized treatment. This gives epinephrine, which acts as a vasoconstrictor, topically to the subglottic edema, and will temporarily decrease edema for a few hours until the treatment wears off.

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25
Q

Causes of acute bronchitis

A

Usually caused by a virus, yet 60% to 90% of patients who seek care receive antibiotics due to their concern about the length of time until the illness self-resolves.

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26
Q

Acute bronchitis presentation

A

Cough, +/- sputum. Initially cannot be distinguished from other upper respiratory tract infections, and tends to persist for 2-3 weeks. Prolonged fever more than a day or two is unusual, and pneumonia should be considered for any systemic ill symptoms in addition to cough. This diagnosis commonly causes wheezing that looks like asthma and responds to bronchodilators! However, it’s not asthma if wheezing only happens in the setting of infection, and would not need controller meds that are always prescribed in the care of asthma. On exam, wheezing may or may not be present, but signs of parenchymal disease should not be, meaning there should be no crackles or areas of dullness or decreased air entry as can be seen in pneumonia.

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27
Q

Diagnostic testing for bronchitis

A

There are no specific tests that need to be done to make a diagnosis of acute bronchitis. In sicker patients that may have bronchopneumonia rather than just bronchitis due to the presence of systemic symptoms (fever, crackles on exam, high respiratory rate, dyspnea, altered mental status) a chest xray should be performed to evaluate for pneumonia, looking for infiltrates in lung parenchyma.

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28
Q

When should bronchitis be treated with antibiotics

A

The only true indication for acute bronchitis to be treated with antibiotics is in treating or preventing Bordetella pertussis, “whooping cough”, as a specific cause

The other infectious cause that is treated with antimicrobials is influenza, and oseltamivir is treatment of choice.

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29
Q

How to treat symptoms of acute bronchitis

A

Ipatropium bromide, a short-acting anticholinergic medication, can be used to decrease symptomatic mucous production and albuterol used to alleviate wheezing.

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30
Q

What is bronchiolitis

A

Bronchiolitis is inflammation and infection of the lower respiratory tract, below the level of the bronchi. It is extremely common, is seen mostly in children < 2 years of age, and is also most severe in this age group.It is exclusively a viral illness, and the most common cause is respiratory syncytial virus (RSV), but it can also be seen with rhinovirus, influenza, human metapneumovirus, parainfluenza virus, etc. It is the most common reason for hospitalization in children! Bronchiolitis is seasonal and is most prevalent Sept-April.

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31
Q

Pathophysiology of bronchiolitis

A

Bronchiolitis causes problems by causing spasm of the bronchiolar smooth muscle, thick secretions, and swelling of the small airways due to intense inflammation.

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32
Q

Presentation and diagnosis of bronchioloitis

A

Young children and infants start with typical cold symptoms and cough, and may progress to wheezing, bronchospastic cough, hypoxia, and respiratory failure. The majority of bronchiolitis is mild, but it can be severe enough to cause total respiratory failure and require ECMO, heart-lung bypass. On examination, crackles are commonly heard throughout all lung fields and wheezing, squeaks, and retractions showing respiratory distress are also common.

Clinical diagnosis

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33
Q

What is pneumonia

A

Infection of the actual parenchyma of the lung, rather than the surrounding structures like bronchi or epithelium only.

The alveoli are filled with congestion and debris, and the septae are thickened, both preventing effective oxygen exchange. This makes hypoxia a cardinal clinical finding in pneumonia.

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34
Q

Stages of pneumonia

A
35
Q

Pathogenesis of pneumonia

A

Pneumonia usually occurs when pathogens are inhaled and evade usual physical and immune barriers to infecting lung tissue, but episodes of bacteremia can also seed lung tissue.

Pneumonia is a serious, deep-seated infection in a very vascular capillary bed, and can spread rapidly and with a virulent course. Pneumonia was a major cause of death in the preantibiotic era, and remains a top 10 cause of death for adults and children.

36
Q

Patterns of penumonia

A

interstitial in pattern, primarily lobar in pattern, or can be diffuse and patchy at the bronchoalveolar level

Look different on X-ray

37
Q

Interstitial pneumonia presentation

A

Interstitial patterns of pneumonia present with insidious onset, dry cough, low to moderate fever, less shortness of breath/hypoxia, and less respiratory distress than other forms of pneumonia, at least initially. The clinical exam usually shows crackles over the entire lung field bilaterally, as the whole lung is involved. This form of pneumonia is more likely to be associated with viral, fungal, and atypical bacterial pathogens than the other forms on examinations.

38
Q

Lobar pneumonia presentation

A

Lobar pneumonia indicates that the entire lobe of the lung, or most of it, has been overtaken with infection. Any lobe can be involved, and multiple lobes can also be involved if it is severe. The clinical findings of decreased air movement, dullness to percussion, egophony, rhonchi, and crackles are commonly seen as well as described on exam questions, and will be limited to the affected area. Patients with lobar pneumonia usually look sicker than patients with interstitial pneumonia, with hypoxia and respiratory distress, and the causes are more “typical” pneumonia pathogens, usually bacterial: Strep pneumoniae, Haemophilus influenzae, group A streptococci, Moraxella catarrhalis, anaerobes, and aerobic gram-negative bacteria

39
Q

Bronchopneumonia presentation

A

Bronchopneumonia pathogens and presentation are very similar to lobar pneumonia, but with more diffusely abnormal lung findings rather than being limited to a single lobe. Similar to lobar pneumonia, these patients will also be sicker at presentation than interstitial pneumonia patients, with respiratory distress and hypoxia.

40
Q

What is comunity acquired pneumonia

A

Pneumonia acquired in a community setting - not hospital, nursing home, etc

41
Q

Clinical presentation of CAP

A

clinical manifestations cannot reliably differentiate the cause,

Cough is a requirement for considering pneumonia

42
Q

How is pneumonia diagnosed

A

A microbiological diagnosis obtained in 50% of CAP cases, with the most commonly recovered pathogens being viruses. Streptococcus pneumoniae the most common bacterial pathogen. Others include: H. influenzae, S. aureus, group A streptococci, Moraxella catarrhalis, anaerobes, and aerobic gram-negative bacteria. Atypical pathogens include Mycoplasma pneumoniae, Legionella spp, Chlamydia pneumoniae, Chlamydia psittaci.

Clinician judgement that the clinical picture may be pneumonia, paired with pneumonia seen on CXR, is how the diagnosis is made.

43
Q

Exam findings for pneumonia

A

Mental status changes (if present, pneumonia is severe!)

RR > 24 b/min

Fever

Crackles or other typical lung findings of pneumonia

Leukocytosis

Completely normal vital signs in a normal adult with cough make pneumonia a very unlikely diagnosis, and another diagnosis should be sought!!

44
Q

Treatment for pneumonia

A

Multiple antibiotics are first-line

Look for specific organisms that have specific medication

45
Q

What is a lung abscess

A

A lung abscess is necrosis and liquefactive necrosis of the parenchyma of the lung due to an infection, usually due to neutrophilic destruction. It obliterates all of the pulmonary structures in its path leaving a cavity, unlike pneumonia that causes infiltration of neutrophils and lymphocytes within the boundaries of existing lung tissue.

46
Q

Causes of lung abscesses

A

They are more likely to be anaerobic bacteria that like to live in the mouth/dental caries, and the abscesses can be polymicrobial, which is unusual in pneumonia. Lung abscesses can also less frequently occur as a complication of severe necrotizing pneumonia, most commonly due to group A strep or MRSA as a complication of influenza or varicella infection.

lung abscesses can be seen in patients who develop obstructive tumors of the bronchi due to inability of the mucociliary mechanism to clear bacteria distal to the obstruction.

47
Q

Clinical presentation of lung abscess

A

The presentation is usually slow and gradual, with the development of fever, cough, sputum production (may be described as foul or putrid), night sweats, and weight loss.

more common in people with risk factors for aspiration: drug or alcohol abuse, neurologic problems, general anesthesia.

48
Q

Diagnosis of lung abscess

A

Chest X-ray shows a lung cavity with air-fluid level, usually in a location that gravity would draw secretions towards when aspiration occurs. Chest CT to get better visualization and evaluate for possible associated obstruction/tumor as a cause is indicated, and if a specific cause is suspected like TB, additional tests may be run

49
Q

Why are lung abscesses not operated on

A

have a high risk of developing fistulas–abnormal, epithelalized tubes connecting spaces that should not be connected. Fistulas as a complication of lung abscesses are very difficult to manage, and can run between the bronchi and pleura or at any point in between.

50
Q

Treatment of lung abscesses

A

Coverage of anaerobes is a must, as is broad-spectrum coverage, so clindamycin is usually used in combination with a beta-lactam antibiotic that is resistant to beta-lactamases (third generation ceph or penicillin/scavenger combo). If MRSA is suspected, vancomycin or linezolid would be added.

51
Q

What is a pleural effusion and types

A

Pleural effusion: A collection of fluid in the pleural space. Many causes, infectious and noninfectious.

Parapneumonic pleural effusion: same, but associated with pneumonia. This occurs in 40% of bacterial pneumonias, and can worsen the outcome.

Empyema: a pleural effusion that is basically pus, often forming a rind on the pleur

52
Q

Pleural effusion on imaging

A

We might suspect it by percussing the lung and finding dullness, but to diagnose it, we get a CXR! If the effusion is >200 mL, you will be able to see it on a plain film. The diaphragms will look like flat fluid levels rather than dome-shaped on an upright film, and the effusion can be bilateral or unilateral.

53
Q

How is the cause of pleural effusion diagnosed

A

Thoracentesis = stick a needle into the fluid collection and drain some off for analysis.

54
Q

Transudate vs exudate

A

Transudate = Starling forces are pushing or pulling fluid out of capillaries, with cells and large proteins staying behind inside the intact capillary wall.

Exudate = the capillary wall is more permeable than usual due to inflammation, and cells, proteins, fluid are all exiting the capillary.

Light’s def of exudate:

Pleural fluid protein/serum protein ratio greater than 0.5, or

Pleural fluid LDH/serum LDH ratio greater than 0.6, or

Pleural fluid LDH greater than two-thirds the upper limits of the laboratory’s normal serum LDH

55
Q

What is pertussis, what is it caused by

A

Whooping cough

Bordetella pertussis and B. parapertussis are the small, gram-negative coccobacilli responsible for this syndrome, about 1% of cases of acute bronchitis in the US.

56
Q

Pertussis presentation

A

This specific respiratory syndrome looks like a cold initially, (catarrhal phase) then turns into coughing paroxysms or prolonged cough (paroxysmal phase) aka “100 day cough” that triggers diagnostic recognition/testing. In babies, pertussis may present with apnea as their respiratory drive fails

57
Q

Treatment of pertussis

A

Once pertussis is diagnosed due to the paroxysmal stage symptoms, intracellularly active macrolide antibiotics(azithromycin, erythromycin, clarithromycin) can be prescribed to decrease spread of the infection to others, but treatment will not alter symptoms or duration or outcome in the patient once the paroxysms are present. Unvaccinated contacts should be treated with prophylactic antibiotics to prevent the development of pertussis.

All adults who will be around babies < 6 months old need a booster shot, because vaccine protection only lasts about 7 years!

58
Q

What is influenza and most xommon complications

A

Caused by influenza A or B viruses, which cause outbreaks and epidemics of various serotypes each year. There are large amounts of virus in respiratory secretions, and droplet transmission occurs via sneezing or coughing.

Influenza is most harmful to those who have complications from the initial influenza infection, and the most common complication is pneumonia. The most common complication is viral, combined viral/bacterial, or secondary bacterial pneumonia.

59
Q

Influenza clinical presentation

A

Classic influenza is the rapid onset of fever, chills, body aches, fatigue, rhinorrhea, and cough

Can progress to ARDS, looks like the rapid development of near-whiteout on the chest x-ray with severe hypoxia and respiratory failure over a matter of hours

60
Q

When is influenza testing done

A

testing if the result will lead to a change in management.

Utility changes based on prevalance -

This means that the test can be helpful when used during flu season when flu infection is common, but won’t be helpful when used when flu prevalence is low.

61
Q

Treatment for influenza

A

The medications used for treatment can cause significant side effects in a large proportion of patients and the overall benefit is greater in hospitalized and fragile patients. The people most in need of treatment are > 65, with chronic heart or lung conditions, or pregnant/postpartum women.

62
Q

Symptoms of COVID-19

A

ever and shortness of breath are more common in patients who need hospitalization than those with a milder course. Fatigue, headache, congestion, runny nose, and muscle aches are the most commonly reported symptoms overall. Unlike many cold virus syndromes, GI distress, diarrhea, and vomiting are more prominent. And, of course, loss of sense of smell and taste is a peculiar and specific finding with this virus as opposed to many other URI viruses.

63
Q

Clinical findings in COVID-19

A

ymphopenia is very common. Elevations of AST, ALT, LDH, CRP, and ferritin indicate increased severity, and elevated D-dimer indicates increased mortality risk. Chest x-ray may show bilateral consolidation, with ground-glass opacities seen bilaterally on CT scans.

64
Q

Risk factors for severe COVID-19 illness

A

Age

Living in a nursing home/longterm care facility

Cardiovascular disease

Diabetes

Chronic respiratory disease

Other underlying serious chronic disease

65
Q

TB clinical presentation

A

Tuberculosis primary infection in immunocompetent hosts most commonly causes a small area of granulomatous consolidation in the mid-lung zones that subsequently undergoes caseous necrosis, with associated mediastinal lymph nodes also becoming infected and necrotic. This process is not overly symptomatic, or may masquerade as a routine respiratory illness

Symptomatic, active TB infection most commonly occurs due to reactivation when the host’s immune system becomes suppressed, and is referred to as reactivation or active TB.

66
Q

Immune response to TB

A

. The major immune response is Th1 mediated (remember this is always the case in granulomatous diseases) and driven by IFN-gamma and tumor necrosis factor. The bacteria then become dormant and can live on in the host for the duration of their life, which is described as “latent TB”. Granulomas with central caseating necrosis are the hallmark of TB, and become calcified over time on chest x-ray.

67
Q

Gold standard for TB diagnosis

A

Demonstration of the acid-fast bacilli in sputum or tissue is the gold standard for diagnosis of active TB.

68
Q
A

TB Granuloma

69
Q

Presentation of acute fungal infection

A

Acute infection is a mild flulike illness with cough that causes granuloma formation and symptoms and findings in the lungs and lymph nodes similar to the Ghon complex of TB and with similar resolution in most patients to a calcified granuloma on chest x-ray.

70
Q

Fungal infection endemic to Ohio river valley

A

Histoplasma capsulatum

71
Q

Histoplasma on histology

A

Histoplasma loves to live inside macrophages, which will be seen on representative images, and are described verbally as round or oval, small yeast forms 2-5 micrometers in diameter. They are a lot smaller than either blasto or coccidio and fit inside of cells as a result, in infected tissue macrophages are typically stuffed with them. You can remember the word “plasma” in Histoplasma and they they are much smaller than plasma cells (lymphocytes) and also love to live inside macrophages, also found in plasma. The majority of histoplasmosis in immune competent people does not require treatment and is a self-limited infection.

72
Q

Coccidioides immitis location and histo

A

Endemic in the southwestern and far western US, particularly the San Joaquin valley in California, where the infection is known as “valley fever.” These appear in pathologic images as thick-walled, nonbudding, always round spherules 20-50 micrometers in diameter (much bigger than histo), and can be filled with small endospores.

73
Q

Blastomyces dermatiditis location and histo

A

This is endemic in areas where Histoplasmosis is also found and is in the same differential for those patients. The fungal forms in tissue are larger than histoplasma, spherical, and are usually described and shown with broad-based budding. Remember Blasto = Broad Based Buds! You can also see the thick wall, but ther are no endospores like with coccidio.

74
Q

Pneumocystis jiroveci pneumonia cause and presentation

A

Caused by Pneumocystis jirovecii, a fungus. The clues are that the patient will usually have oral thrush or other opportunistic infection, AIDS, or another cause for a CD4 cell count less than 200 cells/microL. Serum lactate dehydrogenase (LDH) will also usually be high as an additional clue. The pneumonia looks clinically like an atypical pneumonia usually, with diffuse crackles and diffuse interstitial infiltrate on CXR but cross-sectional imaging in a patient with prolonged infection will show the formation of empty cystic lung spaces

Not in macrophages like histo

75
Q

Treatment for Pneumocystis jiroveci pneumonia

A

The treatment of choice is sulfamethoxazole/trimethoprim

IV corticosteroids are added to patients who are hypoxic at diagnosis with an arterial oxygen tension <60 mmHg , because it provides significant survival benefit,

Patients with CD4+ counts below 200 benefit from Pneumocystis prophylaxis to prevent this complication of immunosuppression.

76
Q

Candida albicans appearance

A

This agent can also be a pathogen in the imunosuppressed, causing an interstitial pneumonia with nodular infiltrates that mimics Pneumocystis jiroveci pneumonia

pseudohyphae and budding yeasts.

77
Q

treatment for candida pneumonia

A

-azole antifungals

78
Q

Common presentation of Cryptococcus neoformans

A

occur more commonly in immunosuppressed people. Exposure to soil, particularly soil with pigeon droppings, is a risk factor, not person to person. Through inhaled spores

79
Q

Cryptococcus neoformans histo

A

thick gelatinous capsule of the fungus resisting staining and standing out as a clear halo when various stains are used, most famously the india ink stain. If the capsule is not seen, then look at the base of the budding yeast. Crypto has a narrow-based bud, unlike blasto with its broad-based buds.

80
Q

What is invasive aspergillosis and presentation

A

more severe spectrum of disease usually seen in immunosuppressed people following inhalation of spores from the environment, including lung transplant recipients. The hallmark of the severe form of IA is invasion of the pulmonary blood vessels, causing coagluative necrosis and hemorrhagic infarction of the lung, including the formation of nodular densities or scarring as the body tries to wall off the infection.

81
Q

Chronic pulmonary aspergillosis presentation

A

look clinically very much like TB, and is usually found either in people who have been treated for TB, or who have COPD or emphysema as an underlying predisposing condition, or chronic steroid use. Basically, anything that creates increased dead space in the airways and impairs mucociliary clearance will increase the risk for this diagnosis

82
Q

Allergic bronchopulmonary aspergillosis (ABPA) presentation

A

cause for severe asthma or worsening formerly stable asthma, and reflects interplay between the immune system and the pathogen as the sensiziation of the immune system to the fungal spores worsen the inflammation of the underlying asthma

Clinically, this manifests as asthma that does not respond as expected to usual stepwise management, and hemoptysis, fever, eosinophilia, and coughing up brown mucus plugs may also be seen. Apergillus-specific IgE are used to help make the diagnosis, with a cutoff of >1000 as likely ABPA

ACUTE angle hyphal branching, tassle like head

83
Q

Cytomegalovirus pneumonia presentation

A

causes pneumonia in immunosuppressed patients

The classic presentation of CMV post-organ transplant is the start of high fever and malaise 40 days post transplant: 40 degrees celsius, 40 days post-transplant. Multiple organs can be affected, in the lung CMV causes an interstitial pneumonia that is severe and progresses to necrosis and sometimes to ARDS.

gigantism of infected cells as well as the nuclei, with an enlarged basophilic nuclear inclusion surrounded by a halo, and called “owl’s eyes.”