Primary inferior vena cava aneurysm
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare primary vascular anomaly, characterized by saccular or rarely fusiform aneurysm of the inferior vena cava. Patients may present with chest pain, abdominal pain, back pain, lower extremity pain and edema, fatigue and fainting. Deep venous thrombosis, penile hemorrhage, paradoxical cerebral embolism and pulmonary embolism can also be observed. It is usually incidentally detected during ultrasound or computed tomography scan examinations or in patients with thromboembolic disease.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Primary inferior vena cava aneurysm | |
| fr | Anévrisme primitif de la veine cave inférieure | |
| de | Primäres Aneurysma der Vena cava inferior | Primäres Aneurysma der unteren Hohlvene |
| es | Aneurisma primario de la vena cava inferior | |
| it | Aneurisma primitivo della vena cava inferiore | |
| nl | Primair aneurysma van vena cava inferior | Primair aneurysma van onderste holle ader |
| pt | Aneurisma primário da veia cava inferior | |
| pl | Pierwotny tętniak żyły głównej dolnej | |
| cs | Primární aneuryzma vena cava inferior | |
| uk | Первинна аневризма нижньої порожнистої вени |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q26.8 | NTBT | attributed | validated |
| MONDO | 0958098 | E | validated | |
| MONDO | 958098 | E | validated | |
| UMLS | C5925120 | 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:95499Congenital anomaly of the inferior vena cava
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/652678
- This record as JSON: /data/d/652678.json