Malignant neoplasms of fallopian tube (Q38918): Difference between revisions

From determinar.ia.br - Determine suas informações
Created a new Item
 
Changed an Item
 
(7 intermediate revisions by the same user not shown)
description / pt-brdescription / pt-br
 
Neoplasias malignas de tuba uterina (trompa de Falópio) são muito menos comuns do que as neoplasias ovarianas correspondentes; entretanto, histologicamente, os mesmos subtipos de tumor epitelial-estromal de superfície são reconhecidos. Os tumores do estroma de cordão sexual e de células germinativas são raros. Molas hidatiformes e coriocarcinoma gestacional são complicações incomuns da gravidez ectópica tubária. O tumor anexial wolffiano também é infrequente e tipicamente ocorre nos folhetos do ligamento largo. Os fatores de risco parecem ser semelhantes aos do ovário. Carcinomas das tubas uterinas são um componente da síndrome hereditária do câncer de ovário-mama causada por mutações da linha germinativa BRCA1 e BRCA2.
description / endescription / en
 
Malignant neoplasms of the fallopian tube are much less common than the corresponding ovarian neoplasms; however, histologically the same surface epithelial-stromal tumour subtypes are recognised. Sex cord-stromal and germ cell tumours are rare. Hydatidiform moles and gestational choriocarcinoma are uncommon complications of tubal ectopic pregnancy. The wolffian adnexal tumour is also infrequent and typically occurs in the leaves of the broad ligament. The risk factors appear similar to those of the ovary. Fallopian tube carcinomas are a component of the hereditary breast-ovarian cancer syndrome caused by BRCA1 and BRCA2 germline mutations.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/459381514 / rank
 
Normal rank
Property / CURIE
 
CID11:2C74
Property / CURIE: CID11:2C74 / rank
 
Normal rank
Property / Canary Token
 
dki-india-2C74
Property / Canary Token: dki-india-2C74 / rank
 
Normal rank
Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank
Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
Normal rank
Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
Normal rank
Property / Linked ICD 10
 
Property / Linked ICD 10: C57.0 / rank
 
Normal rank

Latest revision as of 04:10, 13 August 2026

Malignant neoplasms of the fallopian tube are much less common than the corresponding ovarian neoplasms; however, histologically the same surface epithelial-stromal tumour subtypes are recognised. Sex cord-stromal and germ cell tumours are rare. Hydatidiform moles and gestational choriocarcinoma are uncommon complications of tubal ectopic pregnancy. The wolffian adnexal tumour is also infrequent and typically occurs in the leaves of the broad ligament. The risk factors appear similar to those of the ovary. Fallopian tube carcinomas are a component of the hereditary breast-ovarian cancer syndrome caused by BRCA1 and BRCA2 germline mutations.
Language Label Description Also known as
default for all languages
2C74
    English
    Malignant neoplasms of fallopian tube
    Malignant neoplasms of the fallopian tube are much less common than the corresponding ovarian neoplasms; however, histologically the same surface epithelial-stromal tumour subtypes are recognised. Sex cord-stromal and germ cell tumours are rare. Hydatidiform moles and gestational choriocarcinoma are uncommon complications of tubal ectopic pregnancy. The wolffian adnexal tumour is also infrequent and typically occurs in the leaves of the broad ligament. The risk factors appear similar to those of the ovary. Fallopian tube carcinomas are a component of the hereditary breast-ovarian cancer syndrome caused by BRCA1 and BRCA2 germline mutations.

      Statements

      CID11:2C74
      0 references
      dki-india-2C74
      0 references
      Concluído
      0 references
      13 August 2026
      0 references
      0 references