Case series of three patients with hereditary diffuse gastric cancer in a single family: Three case reports and review of literature

被引:5
作者
Hirakawa, Masahiro [1 ,2 ]
Takada, Kohichi [1 ]
Sato, Masanori [1 ]
Fujita, Chisa [1 ]
Hayasaka, Naotaka [1 ]
Nobuoka, Takayuki [3 ]
Sugita, Shintaro [4 ]
Ishikawa, Aki [5 ]
Mizukami, Miyako [5 ]
Ohnuma, Hiroyuki [1 ]
Murase, Kazuyuki [1 ]
Miyanishi, Koji [1 ]
Kobune, Masayoshi [6 ]
Takemasa, Ichiro [3 ]
Hasegawa, Tadashi [4 ]
Sakurai, Akihiro [5 ]
Kato, Junji [1 ]
机构
[1] Sapporo Med Univ, Dept Med Oncol, Sch Med, Sapporo, Hokkaido 0608556, Japan
[2] Natl Hosp Org, Dept Gastroenterol, Hokkaido Canc Ctr, Sapporo, Hokkaido 0030804, Japan
[3] Sapporo Med Univ, Sch Med, Dept Surg Surg Oncol & Sci, Sapporo, Hokkaido 0608556, Japan
[4] Sapporo Med Univ, Dept Surg Pathol, Sch Med, Sapporo, Hokkaido 0608556, Japan
[5] Sapporo Med Univ, Dept Med Genet, Sch Med, Sapporo, Hokkaido 0608556, Japan
[6] Sapporo Med Univ, Dept Hematol, Sch Med, Sapporo, Hokkaido 0608556, Japan
关键词
Hereditary diffuse gastric cancer; Signet ring cell carcinoma; CDH1; E-cadherin; Endoscopic findings; Case report; CADHERIN GENE CDH1; GERMLINE MUTATIONS; MAGNIFYING ENDOSCOPY; BREAST-CANCER; DIAGNOSIS; SURVEILLANCE; CRITERIA; OUTCOMES;
D O I
10.3748/wjg.v26.i42.6689
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND Hereditary diffuse gastric cancer (HDGC) is a familial cancer syndrome often associated with germline mutations in the CDH1 gene. However, the frequency of CDH1 mutations is low in patients with HDGC in East Asian countries. Herein, we report three cases of HDGC harboring a missense CDH1 variant, c.1679C>G, from a single Japanese family. CASE SUMMARY A 26-year-old female (Case 1) and a 51-year-old male (father of Case 1), who had a strong family history of gastric cancer, were diagnosed with advanced diffuse gastric cancer. After genetic counselling, a 25-year-old younger brother of Case 1 underwent surveillance esophagogastroduodenoscopy that detected small signet ring cell carcinoma foci as multiple pale lesions in the gastric mucosa. Genetic analysis revealed a CDH1 c.1679C>G variant in all three patients. CONCLUSION It is important for individuals suspected of having HDGC to be actively offered genetics evaluation. This report will contribute to an increased awareness of HDGC.
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收藏
页码:6689 / 6697
页数:10
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