Sputum is a mixture of plasma,electrolytes,mucin and water, collected in the first morning 24hr-sputum.
Sputum induction is a method of collecting sputum.
Tracheal aspiration is a method of collecting sputum.
Throat swab is a method of collecting sputum.
Sputum analysis is done on sputum from the upper and lower respiratory tract.
Sputum can betransparent/colorless, normal, yellowgreen, TB, bronchiectasis, green, or pus.
Physical appearance of sputum can also be blood-streaked/ red, TB, bronchiectasis, or rusty/anchovy red, early lobar pneumonia.
Sputum can have an odor that is odorless which is normal, foul/putrid for tumors and cavitaryTB,or sweetish for bronchiectasis and TBcavities, or fruity for P.auruginosa
Sputum can have a certain amount/volume that is scanty, bronchialasthma,acutebronchitis, or ample, bronchiectasis, lung abscess, edema, gangrene, edema or advanced TB.
Sputum can have a certain consistency that is mucoid for asthma, bronchitis, serous/frothy for lung edema, or mucopurulent for bronchiectasis, TB cavities.
Organisms such as P.carinii, T.gondii, S.stercoralis,L.pneumophila,C.neoformans, H.capsulatum,M.tuberculosis,M.pneumoniae, influenza A and B viruses, and respiratorysyncytialvirus can be detected in cytology specimens.
The microscopic appearance of cytology specimens can reveal characteristic amorphous material in LPO and organisms in HPO.
Detection of Pneumocystis carinii in immunosuppressed patients is a clinical significance of cytology specimens.
Eosinophils are less than 1-2% of the differential count in cytology specimens.
Ciliated Columnar BronchialEpithelial cells make up 4-17% of the differential count in cytology specimens.
Lymphocytes make up 1-15% of the differential count in cytology specimens.
Neutrophils are less than 3% of the differential count in cytology specimens.
Fungal elements and viral inclusions may be seen in cytology specimens.
C.neoformans is a significant opportunistic pathogen in patients with AIDS.
AlveolarMacrophages are a hallmark of BAL and make up 56 to 80% of the differential count.
Macroscopic structures found in sputum can include bronchial casts, made of fibrin; Bronchial cast which is a branching tree-like cast found in cases of lobarpneumonia;Cheesymasses, fragments of necrotic pulmonary tissues seen in PTB and pulmonarygangrene;Dittrich’splugs, grayish to yellowish, seen in bronchiectasis and bronchitis, and Pneumolith (lungstones), formed from calcified pulmonary tissues, seen in Histoplasmosis.
Macroscopic structures can also include Curshmann’sspirals, twisted mucoid threads, seen in bronchial asthma, acute bronchitis.
Bronchoalveolarlavage (BAL) is a procedure in obtaining cellular, immunologic & microbiological information from the lower respiratory tract.
Alveolarproteinosis is characterized by PAS positive macrophages.
Charcot-Leyden crystals are observed in asthma.
Bronchoalveolar lavage (BAL) is often used in conjunction with high-resolution computerized tomography (HRCT), medical history and physical examination to determine need for surgical biopsy.
Dense, crystalline concretions are observed in brocholithiasis.
Carchotschlens spirals are observed in asthma.
PAS positive rounded bodies that take silver stain are observed in P.carinii infection.
If delivery to the lab is delayed for longer than 30minutes, specimens from bronchoalveolar lavage (BAL) are transported on ice at 4 o C.
Specimens from bronchoalveolar lavage (BAL) are kept at roomtemperature during transport to the laboratory and processed immediately.
asthma or pulmonaryhypersensitivity reaction is characterized by numerous eosinophils.
Lipid droplets in macrophages are observed in lipoid or aspirationpneumonia.
Chronicbronchitis or bronchiectasis is characterized by numerous eosinophils, abundant mucus, and few or no organisms.
Specimens from bronchoalveolar lavage (BAL) are unacceptable for testing after 24hours.
Alveolarproteinosis is characterized by microscopic formed elements.
Bronchoalveolarlavage (BAL) is particularly useful in evaluating immunocompromised patients, interstitial lung disease, airway diseases, suspected alveolar hemorrhage, pulmonary alveolar proteinosis, Langerhans cell histiocytosis, and dust exposure.
Epithelialcells are mostly found in saliva and are numerous in neutrophils with intra-/extracellular organisms.