Endoscopy 2017; 49(S 01): E14-E15
DOI: 10.1055/s-0042-119397
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© Georg Thieme Verlag KG Stuttgart · New York

Trans-sigmoidal endoscopic ultrasonography-guided fine needle biopsy of a pancreas allograft for the diagnosis of post-transplant lymphoproliferative disorder

Hyungil Seo*
1   Department of Gastroenterology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea
,
Dong Hui Cho*
1   Department of Gastroenterology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea
,
Sun-Ho Lee
1   Department of Gastroenterology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea
,
Jin Ho Shin
2   Department of Surgery, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea
,
Young Hoon Kim
3   Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea
,
Do Hyun Park
1   Department of Gastroenterology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea
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Publikationsverlauf

Publikationsdatum:
09. Januar 2017 (online)

Biopsy of pancreas allografts has a critical role in the evaluation of pancreas allograft dysfunction [1]. However, percutaneous ultrasound or computed tomography (CT)-guided biopsy of a pancreas allograft in the pelvis may not be feasible in some cases. Pelvic lesions are easily imaged endosonographically from the rectum or distal sigmoid colon. Although transrectal endoscopic ultrasonography (EUS)-guided biopsy or drainage for pelvic lesions has been demonstrated to be feasible and safe [2] [3], there have been no reports of lower gastrointestinal EUS-guided fine needle biopsy (FNB) of a pancreas allograft in the pelvis owing to the unique anatomic configuration of the post-transplant anatomy [4].

A 47-year-old man underwent simultaneous pancreas and kidney transplantation 10 years ago for insulin-dependent diabetes mellitus and end-stage renal disease due to diabetic nephropathy. The graft duodenum had been anastomosed to the proximal jejunum to allow for enteric exocrine drainage. The patient presented to us with right lower abdominal pain and elevated levels of amylase and lipase. His abdominopelvic CT scan showed swelling of the pancreas allograft with pancreatic duct dilatation and peripancreatic infiltration ([Fig. 1]). Given this picture, histologic evaluation of the pancreas allograft was mandatory, but the direction of its body and tail, placed towards the right pelvis, was not suitable for percutaneous access. Therefore, we decided to perform a trans-sigmoidal EUS-guided FNB.

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Fig. 1 Abdominopelvic computed tomography (CT) scan showing diffuse swelling and heterogeneous attenuation of the pancreas allograft (white arrows). and its close anatomical relation to the sigmoid colon (white arrowheads).

The procedure was performed after the patient had undergone bowel preparation. A linear echoendoscope was rotated counter-clockwise in the distal sigmoid colon, and the pancreas allograft was visualized in the right pelvis. Trans-sigmoidal EUS-FNB was performed with a 22-gauge needle (ProCore Needle; COOK Medical) ([Fig. 2]; [Video 1]) using the stylet slow-pull technique for a pancreas allograft. A total of four needle passes were made and no procedure-related adverse events were seen.

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Fig. 2 Image during endoscopic ultrasonography-guided fine needle biopsy (EUS-FNB) of the pancreas allograft (black arrowheads).
Video 1: Endoscopic ultrasonography (EUS) performed from the distal sigmoid colon revealed swelling of the pancreas allograft with pancreatic duct dilatation. Parenchymal tissue from the pancreas allograft was obtained with four passes of a 22-gauge needle using the stylet slow-pull technique.

Qualität:

The biopsy revealed monomorphic-type post-transplant lymphoproliferative disorder consistent with Burkitt lymphoma based on histological, immunohistochemical, and fluorescence in situ hybridization (FISH) analysis ([Fig. 3]). After receiving the first cycle of hyper-fractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (Hyper-CVAD), the patient’s lower abdominal pain and elevated pancreatic enzymes were improved.

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Fig. 3 Representative images of the pancreas allograft biopsy. a Histological appearance showing a diffuse infiltration of monomorphic medium-sized tumor cells on hematoxylin and eosin (H&E) staining (magnification × 400). b, c Immunohistochemical staining (magnification × 100) with: b CD20 showing that the tumor cells were of B-cell origin; c Ki-67 showing > 99 % of tumor cells were in proliferation. d Fluorescence in situ hybridization (FISH) analysis showing the c-MYC rearrangement detected by a dual-color, break-apart probe as indicated by the split green and red signals (white arrows) in comparison with unaffected signals (white arrowheads).

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* contributed equally to this work


 
  • References

  • 1 Gaber LW. Pancreas allograft biopsies in the management of pancreas transplant recipients: Histopathologic review and clinical correlations. Arch Pathol Lab Med 2007; 131: 1192-1199
  • 2 Hassan GM, Paquin SC, Albadine R. et al. Endoscopic ultrasound-guided FNA of pelvic lesions: A large single-center experience. Cancer Cytopathol 2016; DOI: 10.1002/cncy.21756.
  • 3 Varadarajulu S, Lee YT. Group EUSW. EUS 2008 Working Group document: evaluation of EUS-guided drainage of pelvic-fluid collections (with video). Gastrointest Endosc 2009; 69: 32-S36
  • 4 Horneland R, Paulsen V, Lindahl JP. et al. Pancreas transplantation with enteroanastomosis to native duodenum poses technical challenges but offers improved endoscopic access for scheduled biopsies and therapeutic interventions. Am J Transplant 2015; 15: 242-250