Atypical pneumonia

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'Atypical pneumonias' are pneumonias that characterize the mismatch between poor physical and extensive X-ray findings (large wedge-shaped infiltrates) with frequent pleural involvement. They are usually viral, chlamydial, mycoplasmal or pneumocystic.

"The term atypical pneumonia is currently considered obsolete and should not be used."It has previously been used to identify pneumonia caused by atypical agents, which is a mislabel, or is used by radiologists to identify pneumonia without a typical X-ray, or is used for unusual pneumonia that does not respond to ATB treatment. Currently the preferred division of pneumonias is for 'nosocomial' , 'community' , 'immunocompromised pneumonia,' pneumonia in social care institutions 'and' ventilator pneumonia . '. [1] Iron

Viral pneumonias[edit | edit source]

Ethiology
  • Respiratory syncytial virus infection – mostly in the winter,
  • parainfluenza in the autumn, winter and spring,
  • flu in the winter,
  • adenoviruses during the whole year
Symptoms
Initially, HCD inflammation is often preceded by wheezing or stridor, cough, signs of difficulty breathing (grunting, alar joint). 'Physical findings' similar to bacterial pneumonias - flu, shortness of breath. 'Laboratory tests' : leukocytes normal or slightly higher (this will not help to differentiate bacterial, but if the leukocytes were significantly elevated, viral inflammation would be unlikely). Severity, X-ray and physical examination do not reliably distinguish between viral and bacterial inflammation.
Diagnosis
Rapid diagnostic tests to detect virus (eg fluorescent antibody test or ELISA test for RSV). 'Virus detection' is important because it sometimes allows the use of a specific antiviral drug. Patients with adenoviral pneumonia may have severe necrotizing pneumonias with pneumocele.
'X-ray of the lungs' - striped perihillosis drawing, accentuated interstitial drawing, peribronchial infiltrates or dispersed bronchopneumonia (but there may also be allaric obscuration as in bacteria).
Complications
Adenovirus pneumonia may be followed by bronchiolitis obliterans 'or' 'severe chronic respiratory failure' . Airway hyperresponsiveness may develop after infection. They can subsequently be complicated by bacterial pneumonia.
Therapy
General supportive treatment as in bacterial, seriously ill patients should be hospitalized. Bacterial superinfection often cannot be completely ruled out, so the co-administration of ATB is indicated. For RSV - ribavirin, for influenza A and B - amantadine.
Prevention and prognosis
Respiratory patients should be vaccinated against influenza A and B annually, children with suspected viral pneumonia should be isolated, and hands should be washed thoroughly.
Most will heal without complications.

Chlamydial pneumonias[edit | edit source]

They are recently becoming more often. They mainly affect infants aged 2-12 weeks. In newborns and infants are usually caused by Chlamydia trachomatis - chlamydia get to the baby from the mother during childbirth. In older children is common Chlamydia pneumoniae - transmission is droplet.

Symptoms
Coughing, tachypnoe, conjunctivitis (but this one is not necessary!), auscultation - crunches, occasionally wheezing, the temperature does not have to be increased. Laboratory tests: eosinophilia, elevated IgM, IgG, IgA.

X-ray of the lungs - diffuse interstitial shading, hyperinflation, multiplication of the peribronchial pattern.

Differential diagnosis
viruses, pneumocystis
Therapy
Erythromycin or sulfisoxazole, treatment must last 14 days. Infants with severe respiratory distress, cough or apnea are hospitalized. Sometimes longer-term oxygen therapy is needed.

Mycoplasma pneumonias[edit | edit source]

The causative agent is Mycoplasma pneumoniae (Eaton's agent). It causes pneumonia mainly in children over 5 years of age. It does not occur in infants under 6 months of age because they have maternal immunoglobulins. It is called "primary atypical pneumonia" - due to the discrepancy between a poor clinical finding and a large X-ray finding. Incubation period is long (2-3 weeks), the onset of problems is gradual.

Symptoms
Fever (above 39° C), cough, headaches, nausea. At first the cough is dry, then the sputum production begins.There may be sore throat, otitis. Auscultation - wheezing, rhonchi, weakened or tube breathing. The disease is mild and is also called "walking pneumonia" (the patient walks with her).
Diagnosis
Leukocytes and differential leukocyte count are usually normal. The diagnosis is supported by the titer of cold hemagglutinins (more than 1:64), as well as a four-fold increase in Ig titer against mycoplasma.
Lung X-ray - interstitial shadowing or bronchopneumonic infiltrates, effusions are rare.
Complications
Affects CNS, blood, skin, heart or joints (autoimmune hemolytic anemia, trombocytopenia, syndrom Guillain-Barré, rash, …).
Therapy
Erythromycin for 7-10 days. Other macrolides (azithromycin and clarithromycin), tetracyclines are also effective.
Prognosis
When there are no complications, the prognosis is excellent, sometimes it subsides spontaneously.

Pneumocystic pneumonias[edit | edit source]

X-ray of pneumocystic pneumonia
Pneumocystis carinii in BAL

Pneumocystis carinii is an infection classified as a fungus (first described by the Pilsen pathologist Vaňek, in 1954). It often occurred in the post-war years in malnourished infants, in nursing homes and in low birth weight children.

Inflammation of the interstitium with a significant "'enlargement of the interalveolar septum" (in which there are plasma cells and lymphocytes). There are foamy eosinophilic proteinaceous substances in the alveoli that contain cysts. The infection is transmitted by droplets, but it can also be obtained from rodents.

'Predisposing factors' : prematurity, malnutrition, chemotherapy, malignancies, long-term treatment with corticosteroids, immunosuppression, anemia, hemophilia, nephrosis,…

Symptoms
The onset is gradual, with non-specific manifestations (restlessness, loss of appetite), there is no cold, cough or fever, tachypnoea and cyanosis appear around the mouth. Severe dyspnoea, tachypnea (80-120 / min) and cyanosis occur within 1-2 weeks. Rhonchi can be heard on the lungs.
X-ray of the lungs - bilateral interstitial striated shadows based on dilated hils, pulmonary hyperinflation.
Diagnosis
Definitive diagnosis by finding evidence of pneumocystis in the lung tissue or in the fluid of respiratory pathways (bronchoscopy, BAL, biopsy), or open lung biopsy or percutaneous lung puncture.
Therapy
Most important remedy is pentamidine (4 mg/kg/den) i. v. or i. m. for 10 - 14 days (60–90 % of patients are cured). It has many side effects – renal dysfunction, hepatic dysfunction, anemia, thrombocytopenia, neutropenia, hypotension, hypoglycaemia, local reactions. Another important drug is cotrimoxazole which has fewer side effects and is just as effective.
Prognosis
The disease lasts 4–6 weeks, and if not treated, the mortality rate is 25-50%. With proper treatment, 50-95% of patients survive.
Prevention
Patients should be isolated from patients with impaired immunity, we perform prophylaxis with cotrimoxazole in endangered patients.

Comparison table for typical and atypical pneumonia[edit | edit source]

PARAMETER TYPICAL PNEUMONIA ATYPICAL PNEUMONIA
Basic characteristics significant physical finding poor physical finding
Agents (extracellular)

Streptococcus pneumoniae, Haemophilus influenzae, Haemophilus parainfluenzae, Staphylococcus aureus, Klebsiella pneumoniae, Escherichia coli and Pseudomonas aeruginosa

(intra/paracellular)

Mycoplasma pneumoniae, Chlamydophila pneumoniae, Chlamydophila psittaci, Legionella pneumophila, Coxiella burnetii, viruses – RSV, influenza, Pneumocystis carinii

Onset sudden after infection of upper respiratory tract, slow
Extrapulmonary symptoms insignificant usual – headaches, myalgia, vomiting, diarrhea
Fever septic febrile subfebrile
Shivering yes rarely
Cough productive dry, irritant
Heart rate sometimes tachycardia normal
Patient looks ill 'normal'
Auscultation crepitus, tracheal breathing, rhonchi sporadic rhonchi
X-ray segmental/lobar obscuration (alveolar involvement) interstitial reticulonodulation (interstitial involvement)
Sedimentation high slightly increased
Inflammatory markers high slightly increased
Blood count leukocytosis]] lymfocytosis
Therapy penicillins macrolides

Links[edit | edit source]

Related articles[edit | edit source]

Sources[edit | edit source]

References[edit | edit source]

  1. ČEŠKA, Richard, et al. Interna. 1. edition. Triton, 2010. 855 pp. pp. 474-475. ISBN 978-80-7387-423-0.