Collecting duct carcinoma
Synonyms: BDC · Bellini carcinoma · Bellini duct carcinoma · CDC
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Collecting duct carcinoma is a rare, aggressive subtype of renal cell carcinoma, which originates from the epithelium of the distal collecting ducts, and usually manifests with hematuria, flank pain, palpable abdominal mass or nonspecific symptoms, such as fatigue, weight loss or fever. Patients are often asymptomatic for long periods of time and therefore, disease is often locally advanced or metastatic at the time of diagnosis. In cases with metastatic spread, bone pain, cough, dyspnea, pneumonia or neurological compromise may be associated.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Collecting duct carcinoma | BDC · Bellini carcinoma · Bellini duct carcinoma · CDC |
| fr | Carcinome des tubes collecteurs | BDC · CDC · Carcinome de Bellini · Carcinome des tubes de Bellini |
| de | Sammelgangkarzinom | DBK · Ductus-Bellini-Karzinom |
| es | Carcinoma de los túbulos colectores | BDC · CDC · Carcinoma de Bellini · Carcinoma de los conductos de Bellini |
| it | Carcinoma dei dotti collettori | Carcinoma dei dotti di Bellini · Carcinoma di Bellini · BDC · CDC |
| nl | Verzamelkanaalcarcinoom | BDC · Bellinicarcinoom · Bellinikanaalcarcinoom · CDC |
| pt | Carcinoma dos ductos coletores | |
| pl | Rak kanalików zbiorczych nerki | BDC · CDC · Rak Belliniego · Rak kanalików Belliniego |
| cs | Karcinom ze sběrných kanálků | BCD · Belliniho karcinom · CDC · Karcinom ze sběrných Belliniho kanálků |
| uk | Збірна протокова карцинома | BDC · Карцинома Белліні · Карцинома протоки Белліні · CDC |
| zh | 集合管癌 | Bellini管癌 |
| tr | Toplayıcı duktus karsinomu | BDC · HKM · Bellini karsinomu · Bellini kanal karsinomu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C64 | NTBT | attributed | validated |
| MONDO | 0005220 | E | validated | |
| UMLS | C1266044 | E | validated | |
| GARD | 9573 | 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:217071Renal cell carcinoma
rare renal diseases; rare neoplastic diseases; rare transplant-related disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | — | Europe | Class only | Validated | RARECARE surveillance of rare cancers in Europe[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/247203
- This record as JSON: /data/d/247203.json