Three synchronous primary carcinomas in a patient with HNPCC associated with a novel germline mutation in MLH1: Case report

Cristian D. Valenzuela, Harvey G. Moore, William C. Huang, Elsa W. Reich, Herman Yee, Harry Ostrer, H. Leon Pachter

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

MLH1 is one of six known genes responsible for DNA mismatch repair (MMR), whose inactivation leads to HNPCC. It is important to develop genotype-phenotype correlations for HNPCC, as is being done for other hereditary cancer syndromes, in order to guide surveillance and treatment strategies in the future. Case presentation: We report a 47 year-old male with hereditary nonpolyposis colorectal cancer (HNPCC) associated with a novel germline mutation in MLH1. This patient expressed a rare and severe phenotype characterized by three synchronous primary carcinomas: ascending and splenic flexure colon adenocarcinomas, and ureteral carcinoma. Ureteral neoplasms in HNPCC are most often associated with mutations in MSH2 and rarely with mutations in MLH1. The reported mutation is a two base pair insertion into exon 10 (c.866_867insCA), which results in a premature stop codon. Conclusion: Our case demonstrates that HNPCC patients with MLH1 mutations are also at risk for ureteral neoplasms, and therefore urological surveillance is essential. This case adds to the growing list of disease-causing MMR mutations, and contributes to the development of genotype-phenotype correlations essential for assessing individual cancer risk and tailoring of optimal surveillance strategies. Additionally, our case draws attention to limitations of the Amsterdam Criteria and the need to maintain a high index of suspicion when newly diagnosed colorectal cancer meets the Bethesda Criteria. Establishment of the diagnosis is the crucial first step in initiating appropriate surveillance for colorectal cancer and other HNPCC-associated tumors in at-risk individuals.

Original languageEnglish (US)
Article number94
JournalWorld Journal of Surgical Oncology
Volume7
DOIs
StatePublished - Dec 8 2009
Externally publishedYes

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Hereditary Nonpolyposis Colorectal Neoplasms
Germ-Line Mutation
Carcinoma
Ureteral Neoplasms
Mutation
DNA Mismatch Repair
Genetic Association Studies
Colorectal Neoplasms
Hereditary Neoplastic Syndromes
Transverse Colon
Nonsense Codon
Base Pairing
Exons
Neoplasms
Colon
Adenocarcinoma
Phenotype
Genes

ASJC Scopus subject areas

  • Oncology
  • Surgery

Cite this

Three synchronous primary carcinomas in a patient with HNPCC associated with a novel germline mutation in MLH1 : Case report. / Valenzuela, Cristian D.; Moore, Harvey G.; Huang, William C.; Reich, Elsa W.; Yee, Herman; Ostrer, Harry; Pachter, H. Leon.

In: World Journal of Surgical Oncology, Vol. 7, 94, 08.12.2009.

Research output: Contribution to journalArticle

Valenzuela, Cristian D. ; Moore, Harvey G. ; Huang, William C. ; Reich, Elsa W. ; Yee, Herman ; Ostrer, Harry ; Pachter, H. Leon. / Three synchronous primary carcinomas in a patient with HNPCC associated with a novel germline mutation in MLH1 : Case report. In: World Journal of Surgical Oncology. 2009 ; Vol. 7.
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