Pneumonia caused by Pseudomonas aeruginosa infection
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare pulmonary disease characterized by primary or nonbacteremic pneumonia most frequently arising in an intensive care setting, or bacteremic pneumonia, which is typically associated with neutropenia. Chronic lower respiratory tract infection with development of episodes of pneumonia is common in patients with cystic fibrosis. Acute infections are potentially life-threatening. Patients present with fever, chills, dyspnea, cyanosis, productive cough, as well as signs of severe systemic toxicity. Alveolar hemorrhage, necrosis, and, eventually, cavity formation, are commonly seen.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pneumonia caused by Pseudomonas aeruginosa infection | |
| fr | Pneumonie due à une infection à Pseudomonas aeruginosa | |
| de | Pneumonie durch Pseudomonas aeruginosa-Infektion | |
| es | Neumonía causada por infección por pseudomonas aeruginosa | |
| it | Polmonite dovuta a infezione da Pseudomonas aeruginosa | |
| nl | Pneumonie veroorzaakt door Pseudomonas aeruginosa-infectie | |
| pt | Pneumonia por Pseudomonas aeruginosa serótipo O11 | |
| pl | Zapalenie płuc wywołane przez Pseudomonas aeruginosa | |
| cs | Pneumonie způsobená infekcí Pseudomonas aeruginosa | |
| uk | Пневмонія, спричинена інфекцією Pseudomonas aeruginosa | |
| zh | 铜绿假单胞菌感染性肺炎 | |
| tr | Psödomonas aeruginosa enfeksiyonunun neden olduğu pnömoni |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | J15.1 | NTBT | attributed | validated |
| ICD-11 | CA40.05 | E | specific | validated |
| MONDO | 0037398 | E | validated | |
| UMLS | C0920182 | E | validated | |
| GARD | 13613 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:101944Rare pulmonary disease
rare respiratory diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-5 / 10 000 | 50 / 100 000 | Europe | Value and class | Validated | European Medicines Agency[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/90066
- This record as JSON: /data/d/90066.json