Cytology:
Histology:
Suppurative and necrotizing inflammation; abscesses with copious, viscous exudate. In invasive liver abscess syndrome dense necrosis without obvious biliary source.
Mucoid variants are associated with worse clinical outcomes and increased antibiotic resistance. They are difficult to eradicate and promote chronic infection and progression.
Hypervirulent Klebsiella can cause primary liver abscess with metastatic spread to eye or CNS, often in diabetes but also in otherwise healthy adults. Mucoid Pseudomonas is typical of chronic airway infection in cystic fibrosis and bronchiectasis. In the lungs of patients with cystic fibrosis, diverse subpopulations of P. aeruginosa often coexist - including mucoid, non-mucoid, and antibiotic-resistant variants.
This microbial heterogeneity poses significant challenges for both treatment and interpretation of culture results.
Contamination: Possible from oropharyngeal or GI flora in non-sterile samples. In sterile sites, clinically significant.
Mucoid appearance reflects abundant extracellular polysaccharide capsule in Klebsiella, alginate in Pseudomonas. Cytomorphology and Gram cannot reliably distinguish Klebsiella from Pseudomonas and other GNR; use ancillary testing. Differential Diagnosis: Non-mucoid Enterobacterales; Serratia/Enterobacter/Escherichia; non-fermenters such as Stenotrophomonas and Achromobacter; yeast with capsule such as Cryptococcus in mucinous background.
The mucoid phenotype of Pseudomonas aeruginosa may be unstable and can revert to a non-mucoid phenotype in vitro or in vivo. Therefore, non-mucoid colony morphology in culture does not reliably exclude mucoid behavior in vivo, particularly in chronic airway or biofilm-associated infection (1).