Background: Rhinoscleroma is a chronic granulomatous infection of the upper airway traditionally considered a monomicrobial disease caused by Klebsiella pneumoniae subsp. rhinoscleromatis. However, limited use of deep-tissue microbiological sampling may have contributed to underrecognition of additional bacterial isolates and microbial complexity. Methods: We report a biopsy-confirmed case of nasal rhinoscleroma in a previously healthy adult. Histopathological evaluation and microbiological analysis were performed on deep intranasal tissue. Bacterial identification was conducted using VITEK 2 and MALDI-TOF mass spectrometry. Antimicrobial susceptibility testing was interpreted according to EUCAST 2025 criteria. Results: Histology demonstrated characteristic Mikulicz cells. Microbiological analysis revealed K. pneumoniae (consistent with subsp. rhinoscleromatis) together with Morganella morganii from deep-tissue biopsy. Importantly, both organisms were also recovered from an independent nasal swab specimen, with concordant antimicrobial susceptibility profiles. M. morganii showed resistance to aminopenicillins and amoxicillin-clavulanate while remaining susceptible to piperacillin-tazobactam, consistent with its intrinsic AmpC β-lactamase profile. Microbiological findings prompted targeted modification of antimicrobial therapy, and targeted therapy with oral levofloxacin was initiated. Conclusion: This case suggests possible microbial complexity in rhinoscleroma and highlights the value of deep-tissue and concordant multi-sample microbiological evaluation. Recognition of co-isolated organisms may have implications for antimicrobial selection and stewardship, although their pathogenic contribution requires further investigation.

Revisiting rhinoscleroma microbiology: a case with concordant dual-specimen bacterial isolation / L. Drago, N.P.. - In: FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY. - ISSN 2235-2988. - 16:(2026 Aug 21), pp. 1-6. [10.3389/fcimb.2026.1837785]

Revisiting rhinoscleroma microbiology: a case with concordant dual-specimen bacterial isolation

L. Drago
Primo
;
F. Mozzanica;L.R. De La Motte;G. Pelosi
Penultimo
;
L. Deflorio
Ultimo
2026

Abstract

Background: Rhinoscleroma is a chronic granulomatous infection of the upper airway traditionally considered a monomicrobial disease caused by Klebsiella pneumoniae subsp. rhinoscleromatis. However, limited use of deep-tissue microbiological sampling may have contributed to underrecognition of additional bacterial isolates and microbial complexity. Methods: We report a biopsy-confirmed case of nasal rhinoscleroma in a previously healthy adult. Histopathological evaluation and microbiological analysis were performed on deep intranasal tissue. Bacterial identification was conducted using VITEK 2 and MALDI-TOF mass spectrometry. Antimicrobial susceptibility testing was interpreted according to EUCAST 2025 criteria. Results: Histology demonstrated characteristic Mikulicz cells. Microbiological analysis revealed K. pneumoniae (consistent with subsp. rhinoscleromatis) together with Morganella morganii from deep-tissue biopsy. Importantly, both organisms were also recovered from an independent nasal swab specimen, with concordant antimicrobial susceptibility profiles. M. morganii showed resistance to aminopenicillins and amoxicillin-clavulanate while remaining susceptible to piperacillin-tazobactam, consistent with its intrinsic AmpC β-lactamase profile. Microbiological findings prompted targeted modification of antimicrobial therapy, and targeted therapy with oral levofloxacin was initiated. Conclusion: This case suggests possible microbial complexity in rhinoscleroma and highlights the value of deep-tissue and concordant multi-sample microbiological evaluation. Recognition of co-isolated organisms may have implications for antimicrobial selection and stewardship, although their pathogenic contribution requires further investigation.
Morganella morganii; Rhinoscleroma; antimicrobial resistance; deep-tissue culture; dual-specimen analysis
Settore MEDS-04/A - Anatomia patologica
21-ago-2026
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1271258
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