# Necrotizing Pneumonia in an Elderly Patient With Chronic Obstructive Pulmonary Disease (COPD): A Case Report

**Authors:** Andreia Salgadinho Machado, Raquel Borrego, Marta Roldão, Marta Anastácio, Sandra André

PMC · DOI: 10.7759/cureus.102563 · Cureus · 2026-01-29

## TL;DR

An elderly COPD patient developed necrotizing pneumonia, requiring multiple antibiotic changes before recovery, highlighting the challenges in treating this severe condition.

## Contribution

This case report emphasizes the complexities of diagnosing and managing necrotizing pneumonia in COPD patients with inconclusive microbiological findings.

## Key findings

- The patient showed clinical improvement after meropenem, but no microbiologic confirmation linked recovery to this antibiotic.
- Necrotizing pneumonia in COPD patients requires individualized treatment and frequent reassessment due to diagnostic uncertainty.
- Broad-spectrum antibiotics like carbapenems should be used cautiously, based on clinical evidence rather than isolated case experiences.

## Abstract

Necrotizing pneumonia (NP) is a severe complication of bacterial pneumonia, characterized by progressive lung necrosis and cavitation. Although advances in imaging and supportive care have improved outcomes, NP remains difficult to manage due to poor antibiotic penetration, frequent polymicrobial infection, and the lack of standardized treatment protocols.

An 85-year-old man with chronic obstructive pulmonary disease (COPD) (Global Initiative for Obstructive Lung Disease (GOLD) group C) and a 40-pack-year former smoking history, managed with long-acting beta-agonist/long-acting muscarinic antagonist (LABA/LAMA), was admitted with acute dyspnea and productive cough. Imaging showed left-sided pneumonia, and methicillin-sensitive Staphylococcus aureus (MSSA) was isolated. Amoxicillin-clavulanate led to transient improvement, but recurrent fever, worsening hypoxemia, and new cavitary lesions developed. Antimicrobial therapy was broadened to piperacillin-tazobactam, vancomycin, and voriconazole, without clinical stabilization. After empiric meropenem, the patient improved, completed 21 days of treatment, and fully recovered. However, without microbiologic confirmation, a direct causal link to meropenem cannot be established.

This case highlights the diagnostic and therapeutic challenges of necrotizing pneumonia in elderly COPD patients, particularly when differentiation between progression, relapse, or superinfection is hampered by inconclusive microbiological findings. Although clinical improvement followed escalation to meropenem, the evidence does not permit attribution of recovery solely to this intervention. These findings reinforce the need for frequent reassessment, individualized treatment strategies, and caution in generalizing therapeutic recommendations from individual case reports.

Early identification of necrotizing complications and timely modification of antimicrobial therapy are critical. Broad-spectrum antibiotics, including carbapenems, should be reserved for cases with compelling clinical or microbiologic evidence of multidrug resistance, rather than being used routinely based on isolated case experiences.

## Linked entities

- **Chemicals:** amoxicillin-clavulanate (PubChem CID 6435924), piperacillin-tazobactam (PubChem CID 461573), vancomycin (PubChem CID 14969), voriconazole (PubChem CID 71616), meropenem (PubChem CID 441130)
- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002), Staphylococcus aureus infection (MONDO:0005545)

## Full-text entities

- **Genes:** SNRNP70 (small nuclear ribonucleoprotein U1 subunit 70) [NCBI Gene 6625] {aka RNPU1Z, RPU1, SNRP70, Snp1, U1-70K, U170K}, SP100 (SP100 nuclear body protein) [NCBI Gene 6672] {aka lysp100b}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLA (Src like adaptor) [NCBI Gene 6503] {aka SLA1, SLAP}, PML (PML nuclear body scaffold) [NCBI Gene 5371] {aka MYL, PP8675, RNF71, TRIM19}, HARS1 (histidyl-tRNA synthetase 1) [NCBI Gene 3035] {aka CMT2W, HARS, HRS, USH3B}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, NUP210 (nucleoporin 210) [NCBI Gene 23225] {aka GP210, POM210}
- **Diseases:** mediastinal (MESH:D008480), renal dysfunction (MESH:D007674), sounds (MESH:D012135), heart disease (MESH:D006331), hypocapnia (MESH:D016857), fungal infection (MESH:D009181), hyperlactatemia (MESH:D065906), necrosis (MESH:D009336), MRSA (MESH:D013203), anemia (MESH:D000740), thrombosis (MESH:D013927), death (MESH:D003643), C (OMIM:211750), viral and mycobacterial infections (MESH:D014777), bronchiectasis (MESH:D001987), infection (MESH:D007239), NP (MESH:D000071067), effusion (MESH:D000080324), weight loss (MESH:D015431), cough (MESH:D003371), Obstructive Lung Disease (MESH:D008173), pleural effusion (MESH:D010996), cavitary lesion (MESH:C566924), type I respiratory failure (MESH:D012131), lymphadenopathy (MESH:D008206), infiltrates (MESH:D017254), autoimmune diseases (MESH:D001327), chest pain (MESH:D002637), COPD (MESH:D029424), fatigued (MESH:D005221), pneumonia (MESH:D011014), bacterial pneumonia (MESH:D018410), secondary immunodeficiency (MESH:D000068376), ischemia (MESH:D007511), pulmonary embolism (MESH:D011655), hematologic malignancies (MESH:D019337), fever (MESH:D005334), systolic murmur (MESH:D054160), hypoxemia (MESH:D000860), inflammation (MESH:D007249), respiratory infection (MESH:D012141), fibrosis (MESH:D005355), dyspnea (MESH:D004417), diminished (MESH:D015354), lung damage (MESH:D008171), diabetes mellitus (MESH:D003920), pulmonary tissue (MESH:D055370), edema (MESH:D004487)
- **Chemicals:** carbon dioxide (MESH:D002245), LABA/ (-), piperacillin-tazobactam (MESH:D000077725), HCO3 (MESH:D001639), carbapenem (MESH:D015780), Vancomycin (MESH:D014640), meropenem (MESH:D000077731), norepinephrine (MESH:D009638), voriconazole (MESH:D065819), methicillin (MESH:D008712), clarithromycin (MESH:D017291), Oxygen (MESH:D010100), galactomannan (MESH:C012990), Amoxicillin-clavulanate (MESH:D019980)
- **Species:** Legionella pneumophila (species) [taxon 446], Staphylococcus aureus (species) [taxon 1280], Mycobacterium tuberculosis (species) [taxon 1773], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Streptococcus pneumoniae (species) [taxon 1313], Klebsiella pneumoniae (species) [taxon 573]

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## Figures

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## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949605/full.md

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Source: https://tomesphere.com/paper/PMC12949605