Ovarian fibroma
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare benign ovarian tumor of sex cord / stromal origin characterized by an abdominal mass which may present with abdominal pain, distension, or menorrhagia, among others, or may also be asymptomatic. Association with ascites and hydrothorax is known as Meigs syndrome. The tumor can be solid and/or cystic in nature. Histologically it features bundles of spindle cells forming variable amounts of collagen, without cellular atypia or atypical mitoses.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Ovarian fibroma | |
| fr | Fibrome ovarien | |
| de | Ovarialfibrom | |
| es | Fibroma ovárico | |
| it | Fibroma ovarico | |
| nl | Ovarieel fibroom | |
| pt | Fibroma ovárico | |
| pl | Włókniak jajnika | |
| cs | Ovariální fibrom | |
| uk | Фіброма яєчника | |
| zh | 卵巢纤维瘤 | |
| tr | Over fibromu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D27 | NTBT | attributed | validated |
| ICD-11 | 2F32.1 | E | specific | validated |
| MONDO | 0008168 | E | validated | |
| MeSH | C562391 | E | validated | |
| UMLS | C0149951 | E | validated | |
| MedDRA | 10064257 | 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:97293Rare benign ovarian tumor
rare neoplastic diseases; rare gynecological and obstetric 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 | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
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
11 annotations · validated 2016-01-20| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0003270 | Abdominal distention | |
| HP:0002027 | Abdominal pain | |
| HP:0000137 | Abnormality of the ovary | |
| HP:0010618 | Ovarian fibroma | |
| HP:0002202 | Pleural effusion | |
| Frequent (79-30%) | ||
| HP:0001541 | Ascites | |
| HP:0002671 | Basal cell carcinoma | |
| HP:0008703 | Gonadal calcification | |
| HP:0030451 | Mesenteric cyst | |
| HP:0010603 | Odontogenic keratocysts of the jaw | |
| HP:0002586 | Peritonitis | |
Run the differential on the 5 obligate / very frequent terms
Annotation source: 3951494[PMID]_1256472[PMID]_24602407[PMID]_18501324[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/314473
- This record as JSON: /data/d/314473.json