Search
Descriptor English: Dysgerminoma
Descriptor Spanish: Disgerminoma
Descriptor disgerminoma
Scope note: Neoplasia ovárica maligna, que se considera derivada de células germinales primordiales de la gónada embrionaria sexualmente indiferenciada. Se corresponde con el seminoma testicular clásico, siendo idéntico a este macroscópica e histológicamente. Los disgerminomas constituyen el 16 por ciento de todos los tumores de células germinales, pero son raros en niños menores de 10 años, aunque cerca del 50 por ciento ocurren en menores de 20 años. Generalmente se considera que tienen bajo grado de malignidad, pero el tumor puede diseminarse si traspasa su cápsula y afecta a los ganglios linfáticos o los vasos sanguíneos. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p. 1646)
Descriptor Portuguese: Disgerminoma
Descriptor French: Dysgerminome
Entry term(s): Disgerminoma
Disgerminomas
Dysgerminomas
Tree number(s): C04.557.465.330.300
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D004407
Scope note: A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646)
Annotation: coordinate with probably OVARIAN NEOPLASMS
Allowable Qualifiers: BL blood
BS blood supply
CF cerebrospinal fluid
CH chemistry
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SC secondary
SU surgery
TH therapy
UL ultrastructure
UR urine
VE veterinary
VI virology
Public MeSH Note: 79; was DISGERMINOMA 1963-78
Online Note: use DYSGERMINOMA to search DISGERMINOMA 1966-78
History Note: 79; was DISGERMINOMA 1963-78
DeCS ID: 4470
Unique ID: D004407
NLM Classification: WP 322
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1979/01/01
Date of Entry: 1999/01/01
Revision Date: 2003/07/09
Dysgerminoma - Preferred
Concept UI M0006918
Scope note A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646)
Preferred term Dysgerminoma
Entry term(s) Disgerminoma
Disgerminomas
Dysgerminomas



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.


Go to survey