Intraductal tubulopapillary neoplasm of the pancreas with somatic BRAF mutation

被引:0
作者
Urata, Takahiro [1 ]
Naito, Yoshiki [2 ]
Nagamine, Michiko [3 ]
Izumi, Yoshihiro [4 ]
Tonaki, Ginga [1 ]
Iwasaki, Hajime [1 ]
Sasaki, Akiko [1 ]
Yamasaki, Akira [1 ]
Minami, Nobuhiro [1 ]
Yoshioka, Rituko [1 ]
Kitada, Hideki [1 ]
Takekuma, Yoshi [1 ]
Yokomizo, Hiroshi [5 ]
Fukuda, Seiji [3 ]
Yamaguchi, Hiroshi [6 ]
Kuboki, Yuko [7 ]
Furukawa, Toru [7 ]
Hifumi, Michio [1 ]
机构
[1] Japanese Red Cross Kumamoto Hosp, Dept Gastroenterol, 2-1-1 Nagamine Minami, Kumamoto, Kumamoto 8618520, Japan
[2] Kurume Univ, Sch Med, Dept Pathol, Kurume, Fukuoka, Japan
[3] Japanese Red Cross Kumamoto Hosp, Dept Pathol, Kumamoto, Japan
[4] Tamana Reg Hlth Med Ctr, Dept Gastroenterol, Kumamoto, Japan
[5] Japanese Red Cross Kumamoto Hosp, Dept Surg, Kumamoto, Japan
[6] Saitama Med Univ, Saitama Int Med Ctr, Dept Pathol, Hidaka, Japan
[7] Tokyo Womens Med Univ, Inst Integrated Med Sci, Tokyo, Japan
关键词
Pancreas; Intraductal tubulopapillary neoplasm; Microinvasion; Recurrence; BRAF;
D O I
10.1007/s12328-012-0342-1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Intraductal tubulopapillary neoplasm (ITPN) is a rare pancreatic tumor belonging to a newly recognized entity that is coined in the 2010 WHO classification. We present a case of ITPN-associated microinvasive adenocarcinoma that developed in an asymptomatic 78-year old patient. The tumor demonstrated all the clinical, radiological, and pathological characteristics of ITPN, but it differs from other reported cases of ITPN in molecular analysis, which revealed a somatic mutation in BRAF (c.1799T>A; p.V600E) but no mutation in PIK3CA. Post- operative recurrence was discovered 34 months after tumor resection with negative margins and a 6-month course of adjuvant chemotherapy. To the best of our knowledge, this is the first case of ITPN with BRAF mutation. This case suggests that an activation of RASmitogen-activated protein kinase signaling pathway may play a role in development of some of ITPNs. A possible mechanism of tumor recurrence in ITPN is also discussed. Further case series with molecular study are awaited to delineate the clinicopathological and molecular characteristics of ITPN.
引用
收藏
页码:413 / 420
页数:8
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