[A Case of Diagnosed Lynch Syndrome in a Patient with Ureteral Cancer].
Journal
Hinyokika kiyo. Acta urologica Japonica
ISSN: 0018-1994
Titre abrégé: Hinyokika Kiyo
Pays: Japan
ID NLM: 0421145
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
entrez:
16
7
2021
pubmed:
17
7
2021
medline:
20
7
2021
Statut:
ppublish
Résumé
Lynch syndrome (LS) is an autosomal dominant genetic disorder in which tumors are known to develop at an early age. Upper tract urothelial carcinoma is one of the tumors related to Lynch syndrome. A 49-year-old woman visited a urologic clinic due to left abdominal pain. She had a history of ovarian cancer. Her mother had a history of colorectal cancer and renal pelvic cancer, and her grandmother had had colorectal cancer. After detailed examination, she received laparoscopic left nephroureterectomy and she was pathologically diagnosed with left ureteral cancer. LS was suspected based on her past history, family history, and age. A microsatellite instability (MSI) test gave a positive result, and genetic analysis confirmed a mutation in the MSH2 gene, leading to the diagnosis of Lynch syndrome. Although LS has a high frequency of carcinogenesis, it is thought that an improved prognosis can be achieved by early discovery and treatment of cancer in LS patients. From our case report, we recommend screening of LS in patients with a past/family history, who have had an upper tract urothelial carcinoma. Once LS is diagnosed, the patient should be followed by a planned surveillance of cancer development.
Identifiants
pubmed: 34265897
doi: 10.14989/ActaUrolJap_67_6_229
doi:
Types de publication
Case Reports
Journal Article
Langues
jpn
Sous-ensembles de citation
IM