Endoscopy 2021; 53(09): E322-E323
DOI: 10.1055/a-1275-9603
E-Videos

Severe acute pancreatitis caused by endoscopic ultrasonography-guided fine-needle biopsy of a pancreatic solid pseudopapillary neoplasm

Su Luo
1   Department of Gastroenterology, Shenzhen Peopleʼs Hospital, Shenzhen, Guangdong, China
,
De-feng Li
1   Department of Gastroenterology, Shenzhen Peopleʼs Hospital, Shenzhen, Guangdong, China
,
Liliangzi Guo
2   Department of Gastroenterology, The First Affiliated Hospital, Jinan University, Guangzhou, Guangdong, China
,
Lu Bai
1   Department of Gastroenterology, Shenzhen Peopleʼs Hospital, Shenzhen, Guangdong, China
,
Li-sheng Wang
1   Department of Gastroenterology, Shenzhen Peopleʼs Hospital, Shenzhen, Guangdong, China
,
Jun Yao
1   Department of Gastroenterology, Shenzhen Peopleʼs Hospital, Shenzhen, Guangdong, China
› Author Affiliations

A 33-year-old man was admitted to our hospital for investigation of a mass in the pancreatic tail found on computed tomography (CT) scan 3 months previously. Endoscopic ultrasonography (EUS) revealed a 3.0 × 3.1-cm hypoechoic lesion in the tail of the pancreas, with no wall nodules, separation, or communication with the pancreatic duct ([Fig. 1]). EUS-guided fine-needle biopsy (EUS-FNB) was performed with a 22G ultrasound biopsy needle with a side hole (ECHO-HD-22-C; Cook Echotip ProCore). We obtained sufficient tissue with no cystic fluid by puncturing the lesion three times, each time under 5-mL negative pressure with 15 to 20 insertions ([Video 1]). The mass was eventually diagnosed as a solid pseudopapillary tumor on pathology with immunohistochemical staining ([Fig. 2]).

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Fig. 1 Endoscopic ultrasonography image showing a hypoechoic lesion in the tail of the pancreas.

Video 1 Endoscopic ultrasonography-guided fine-needle biopsy (EUS-FNB) being performed on a hypoechoic lesion in the tail of the pancreas.


Quality:
Zoom Image
Fig. 2 Pathological appearance of the biopsy specimen taken from the mass, which was diagnosed as being a solid pseudopapillary tumor.

Unfortunately, the patient developed severe acute pancreatitis after undergoing the EUS-FNB. This was confirmed by an elevation in the patient’s blood leukocyte and amylase levels, and on CT scanning ([Fig. 3]). His symptoms were accompanied by type I respiratory failure and high grade fever for 7 days, but the patient eventually recovered after continuous renal replacement therapy, along with other treatments.

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Fig. 3 Computed tomography scan of the abdomen showing exudation around the tail of the pancreas, confirming the diagnosis of acute pancreatitis.

Compared with EUS-guided fine-needle aspiration (EUS-FNA), EUS-FNB is more appropriate for the diagnosis of pancreatic lesions because it can obtain more specimens and has a higher diagnostic accuracy, with no difference in the reported incidence of complications [1]. We used the 22G needle to increase the diagnostic accuracy and technical success rate during the EUS-FNB procedure, while reducing complications [2].

We consider there are several possible reasons for the occurrence of serious complications. The side hole of the needle used may have obtained some tissue and increased the chance of cutting off the pancreatic duct. The CT scan shows that, although the pancreas is not obviously swollen, the extravasation of cystic fluid through the ruptured wall of the mass caused peritonitis. Excessive needle insertions and punctures may also cause pancreatitis [3]. This case sends a reminder that the safety of EUS-FNB for cystic–solid lesions should be re-evaluated.

Endoscopy_UCTN_Code_CPL_1AL_2AD

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Publication History

Article published online:
23 October 2020

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  • References

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  • 2 Li DF, Wang JY, Yang MF. et al. Factors associated with diagnostic accuracy, technical success and adverse events of endoscopic ultrasound-guided fine-needle biopsy: A systematic review and meta-analysis. J Gastroenterol Hepatol 2020; 35: 1264-1276
  • 3 Lee KH, Kim EY, Cho J. et al. Risk factors associated with adverse events during endoscopic ultrasound-guided tissue sampling. PloS One 2017; 12: 1-13