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Genetic analysis of postoperative recurrence of pancreatic cancer potentially owing to needle tract seeding during EUS-FNB.
Kawabata, Hidemasa; Miyazawa, Yuki; Sato, Hiroki; Okada, Tetsuhiro; Hayashi, Akihiro; Iwama, Takuya; Fujibayashi, Shugo; Goto, Takuma; Sasajima, Junpei; Takauji, Shuhei; Fujiya, Mikihiro; Torimoto, Yoshihiro; Tanino, Mishie; Omori, Yuko; Ono, Yusuke; Karasaki, Hidenori; Mizukami, Yusuke; Okumura, Toshikatsu.
  • Kawabata H; Department of Medicine.
  • Miyazawa Y; Oncology Center.
  • Sato H; Department of Medicine.
  • Okada T; Department of Medicine.
  • Hayashi A; Department of Medicine.
  • Iwama T; Institute of Biomedical Research, Sapporo-Higashi Tokushukai Hospital, Sapporo, Hokkaido, Japan.
  • Fujibayashi S; Department of Medicine.
  • Goto T; Oncology Center.
  • Sasajima J; Department of Medicine.
  • Takauji S; Department of Medicine.
  • Fujiya M; Department of Medicine.
  • Torimoto Y; Department of Medicine.
  • Tanino M; Department of Medicine.
  • Omori Y; Department of Medicine.
  • Ono Y; Oncology Center.
  • Karasaki H; Department of Surgical Pathology, Asahikawa Medical University, Asahikawa, Hokkaido, Japan.
  • Mizukami Y; Department of Investigative Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Okumura T; Department of Medicine.
Endosc Int Open ; 7(12): E1768-E1772, 2019 Dec.
Article en En | MEDLINE | ID: mdl-31828215
ABSTRACT
Background and study aims Needle tract seeding during endoscopic ultrasound fine-needle biopsy (EUS-FNB) remains a concern. We investigated whether such seeding occurred in a patient with pancreatic ductal adenocarcinoma (PDA). Patient and methods Surgically resected and EUS-FNB-derived specimens were genotyped to determine if a gastric wall tumor that emerged 3 years after curative resection of an early-stage PDA was clonally related to the original tumor. Results The gastric tumor histologically resembled the primary PDA; the lesions also shared KRAS , SMAD4 , and RNF43 mutations. Genotyping of the preoperative EUS-FNB specimen, in which cancer was not detected, nevertheless revealed mutations that were identical to those in the resected primary and recurrent tumors. While the primary PDA had a low frequency of mutant SMAD4 , such mutations were highly prevalent in both the EUS-FNB and recurrent tumor specimens. Conclusions The genetic lineages of sampled tissues from our patient revealed that needle tract seeding may have incidentally occurred when a subset of neoplastic cells within a heterogeneous tumor ( i. e. , an aggressive clone) was targeted during EUS-FNB.