Pituitary dermoid and epidermoid cysts
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adult, Elderly
- Status
- active
Pituitary dermoid and epidermoid cysts is a rare, acquired pituitary hormone deficiency characterized by the presence of rare, benign tumor in the sellar region. Clinical presentation is either acute or insidious, and is variable according to the cyst location, size and potential rupture. Most commonly patients present with headache, visual disturbances, and pituitary dysfunction.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pituitary dermoid and epidermoid cysts | |
| fr | Kystes dermoïde et épidermoïde de l'hypophyse | |
| de | Hypophysen- und Epidermoidzysten | |
| es | Quistes hipofisarios dermoides y epidermoides | |
| it | Cisti ipofisarie dermoidi ed epidermoidi | |
| nl | Hypofysaire dermoïde en epidermoïde cysten | |
| pt | Quistos pituitários dermóides e epidermóides | |
| pl | Torbiele skórzaste i nabłonkowe przysadki | |
| cs | Dermoidní a epidermoidní cysty hypofýzy | |
| uk | Дермоїдні та епідермоїдні кісти гіпофіза | |
| zh | 垂体皮样囊肿和表皮样囊肿 | |
| tr | Hipofiz dermoid ve epidermoid kistler |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D35.2 | NTBT | attributed | validated |
| ICD-11 | 5A61.0 | NTBT | index | validated |
| MONDO | 0019615 | E | validated | |
| UMLS | C5190781 | 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 (2):
- ORPHA:100091Adrenal/paraganglial tumor
rare endocrine diseases; rare neoplastic diseases - ORPHA:95503Pituitary hormone deficiency of tumoral origin
rare endocrine 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
24 annotations · validated 2017-02-08| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0000830 | Anterior hypopituitarism | |
| HP:0010885 | Avascular necrosis | |
| HP:0002017 | Nausea and vomiting | |
| HP:0011750 | Neoplasm of the anterior pituitary | |
| Frequent (79-30%) | ||
| HP:0000141 | Amenorrhea | |
| HP:0000651 | Diplopia | |
| HP:0012505 | Enlarged pituitary gland | |
| HP:0100829 | Galactorrhea | |
| HP:0003324 | Generalized muscle weakness | |
| HP:0010514 | Hyperpituitarism | |
| HP:0000135 | Hypogonadism | |
| HP:0000870 | Increased circulating prolactin concentration | |
| HP:0000876 | Oligomenorrhea | |
| HP:0000871 | Panhypopituitarism | |
| HP:0002331 | Recurrent paroxysmal headache | |
| HP:0007663 | Reduced visual acuity | |
| HP:0030907 | Thunderclap headache | |
| Occasional (29-5%) | ||
| HP:0011442 | Abnormality of central motor function | |
| HP:0011730 | Abnormality of central sensory function | |
| HP:0001287 | Meningitis | |
| HP:0000798 | Oligozoospermia | |
| HP:0001250 | Seizure | |
| Very rare (<4-1%) | ||
| HP:0001959 | Polydipsia | |
| HP:0001117 | Sudden loss of visual acuity | |
Run the differential on the 4 obligate / very frequent terms
Annotation source: 11081162[PMID]_1886651[PMID]_15808736[PMID]_9384413[PMID]_9864727[PMID]_2417151[PMID]_6827329[PMID]_6661939[PMID]_15808736[PMID]_18701295[PMID]_25865027[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/91351
- This record as JSON: /data/d/91351.json