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Gastric outlet obstruction secondary to solid-pseudopapillary neoplasm of the pancreas in an eight year old child. Report of a case

  • Rick Bidassek1,
  • Herbert Spelter1,
  • Daniel Gödde2,
  • Hubert Zirngibl1 and
  • Peter C. Ambe1Email author
Diagnostic Pathology201611:7

https://doi.org/10.1186/s13000-016-0465-7

Received: 3 November 2015

Accepted: 14 January 2016

Published: 20 January 2016

Abstract

Background

Solid pseudopapillary neoplasm is a rare cystic tumor of the exocrine pancreas. Abdominal pain or discomfort is the most common symptom, usually in young females.

Case presentation

Herein we report the case of an 8 - year old child presenting with symptoms of gastric outlet obstruction.

Conclusion

A solid pseudopapillary neoplasm of the pancreatic caput was diagnosed and surgically removed.

Keywords

PancreasPancreatic tumorSolid pseudopapillary neoplasmGastric outlet obstructionImmunohistochemistry

Background

Solid pseudopapillary neoplasm (SPN) is a rare cystic tumor of exocrine pancreas with a female predominance. Clinically, it presents as a mass in the pancreas with a wide range of symptoms. Surgical exploration is indicated to release the intra-abdominal extrusion and for histopathology. SPN to the best of our knowledge has so far not been reported in patients below 9 years of age. Besides, gastric outlet obstruction has not been reported as the first sign of SPN.

Case presentation

An 8-year old female patient presented in the pediatric unit with abdominal discomfort, nausea and bitter vomitus. Physical examination revealed a mass in the abdomen. Abdominal ultrasound sonography revealed a 3 cm large mass in the head of the pancreas. Endoscopic sonography confirmed a cystic tumor of the pancreatic caput and fine needle biopsies were taken for histopathology, Fig. 1a & b. Blood chemistry revealed elevated c-reactive protein (CRP: 7.2 mg/dl; normal range <0.5 mg/dl) and high white blood count (WBC: 16.2/nl; normal range: 4–10/nl). Serum lipase was mildly elevated (179 U/l; normal range: < 60 U/l). All liver enzymes including bilirubin were within normal range. Equally, the tumor markers carbohydrate antigen 19–9 (CA 19–9), carcinoembryonic antigen (CEA) and chromogranin A were within normal limits.
Fig. 1

Findings from ultrasound sonography. a trans abdominal ultrasound sonography showing a mass in the pancreatic caput. b endoscopic sonography of the pancreas confirmed a large mass in the head of the pancreas

Magnet resonance imaging (MRI) of the abdomen showed a thick-walled, cystic mass in the head of the pancreas with compression of the duodenum, Fig. 2ac. Histopathology from the fine needle biopsies was inconclusive. The case was discussed at the interdisciplinary board and surgical exploration was recommended.
Fig. 2

MRI scans in coronary. * SPN. a sagittal b tranversal c reconstruction

A well capsulated mass of the pancreatic head without macroscopic signs of malignancy was found and completely enucleated during laparotomy, Fig. 3. Surgery and recovery were uneventful and the patient was discharged 7 days later with normal pancreatic function.
Fig. 3

Intraoperative finding

Histopathology confirmed the diagnosis of SPN following positive stains on immunohistochemistry with antitrypsin, vimentin, beta-catenin, CD 56 and CD 10, Fig. 4af.
Fig. 4

Histopathology and immunohistochemistry: a Hematoxylin and eosin. b Immunostaining for Antitrypsin. c Immunostaining for Beta-catenin. d Immunostaining for CD 10. e Immunostaining for CE 56. f Immunostaining for Vimentin

Discussion

SPN of the pancreas was first reported by Lichtenstein in 1934 [1]. In 1996 SPN was recognized by the World Health Organization as an independent histopathologic entity.

The incidence of SPN varies widely amongst reported series. Cubilla and Fitzerald [2] reported a 0.17 % incidence for SPN in a series of 645 pancreatic neoplasms. Morohoshi et al. [3] reported seven cases of SPN (2.7 %) after analyzing 264 pancreatic tumors. In yet another series of 336 cases, 1.48 % incidence of SPN was reported by Sheeham and colleagues [4]. Because all these incidences are based on adult or mixed population, the incidence of SPN in the pediatric population is estimated to be way below the 0.17 % reported by Cubilla and Fitzerald [2]. This notion is supported a report by Lack et al., who found just one case of SPN in a 30 - year review of data from the Boston Children’s Hospita [5].

The limited amount of publications on SNP is a reflection of the rare nature of this entity. In fact, a vast majority of the medical literature on this entity consists of case reports and small case series. The largest series so far is a review by Papavramidis et al. [6] including 718 cases. In this series, the prevalence of SPN was higher in female patients with a female to male ration of 10:1. The mean age at the time of diagnosis in this series was 22 years. Although an age range from 2 to 84 years was reported in their review, no single publication on SPN in a patient below the age of 9 years could be found in the English literature.

Although SPN can be clinically silent, patients might present with a mass in the upper abdomen with discomfort or pain [7]. Physical examination may reveal a mass in the mid abdomen. This is usually seen on ultrasound sonography. Endoscopic sonography with fine needle biopsy for histopathology might be helpful. The tumor is usually identified on MRI or computed tomography. Surgical exploration and resection is the mainstay of treatment [8, 9]. Surgical excision is directed towards symptom relief as well as to confirm the on histopathology and role out other malignant pancreatic lesions.

On like in other reports, signs of gastric outlet obstruction, i.e. mechanical obstruction of the upper gastro-intestinal tract with recurrent bitter vomitus in this case heralded SPN. Although no enzymatic analysis of the vomitus for bile of gastric enzymes was performed, the bitter nature of the vomitus suggested a proximal gastro-intestinal obstruction. This was confirmed by the identification of a large mass in the pancreatic head with duodenal compression (Fig. 3). A well-encapsulated mass of the pancreatic caput was completely enucleated during surgical exploration. Histopathology and immunohistochemistry confirmed the mass to be an SPN.

There are two distinctive findings in this case: the age at the time of presentation and the initial symptom. This to the best of our knowledge is the first reported case of SPN in a patient below nine years. The child in this case was eight years old at the time of diagnosis and gastric outlet obstruction has not been previously reported as an initial presentation of SPN.

Conclusion

Taken together, this is the first reported case of SPN in a child below the age of nine presenting with bitter vomitus as a sign of gastric outlet obstruction. An interdisciplinary board should discuss all such cases. Surgical exploration with the goal of releasing symptoms is the main stay of treatment. Although SPN is mostly benign, there is a minimal risk of malignant transformation. Therefore, histopathology with immunohistochemical staining should be performed to confirm the diagnosis of SPN and role out malignant pancreatic tumors.

Consent

Written informed consent was obtained from the patient´s legal representatives for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal”.

Abbreviations

CA: 

carbohydrate antigen

CEA: 

carcinoembryonic antigen

CRP: 

C-reactive protein

MRI: 

magnet resonance imaging

SPN: 

solid pseudopapillary neoplasm

WBC: 

white blood count

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Helios Klinikum Wuppertal, Department of Surgery II, Witten – Herdecke University, Wuppertal, Germany
(2)
Institute of Pathology and Molecular Pathology, Helios Klinikum Wuppertal, Witten – Herdecke University, Wuppertal, Germany

References

  1. Lichtenstein L. Papillary cystadenocarcinoma of pancreas: case report, with notes on classification of malignant cystic tumors of pancreas. Am J Cancer. 1934;21(3):542–53.View ArticleGoogle Scholar
  2. Cubilla AL, Fitzgerald PJ. Cancer of the pancreas (nonendocrine): a suggested morphologic classification. Semin Oncol. 1979;6(3):285–97.PubMedGoogle Scholar
  3. Morohoshi T, Kanda M, Horie A, Chott A, Dreyer T, Kloppel G, et al. Immunocytochemical markers of uncommon pancreatic tumors. Acinar cell carcinoma, pancreatoblastoma, and solid cystic (papillary-cystic) tumor. Cancer. 1987;59(4):739–47.PubMedView ArticleGoogle Scholar
  4. Sheehan MK, Beck K, Pickleman J, Aranha GV. Spectrum of cystic neoplasms of the pancreas and their surgical management. Arch Surg. 2003;138(6):657–60. discussion 660–652.PubMedView ArticleGoogle Scholar
  5. Lack EE, Cassady JR, Levey R, Vawter GF. Tumors of the exocrine pancreas in children and adolescents. A clinical and pathologic study of eight cases. Am J Surg Pathol. 1983;7(4):319–27.PubMedView ArticleGoogle Scholar
  6. Papavramidis T, Papavramidis S. Solid pseudopapillary tumors of the pancreas: review of 718 patients reported in English literature. J Am Coll Surg. 2005;200(6):965–72.PubMedView ArticleGoogle Scholar
  7. Nasher O, Hall NJ, Sebire NJ, de Coppi P, Pierro A. Pancreatic tumours in children: diagnosis, treatment and outcome. Pediatr Surg Int. 2015;31(9):831–5.PubMedView ArticleGoogle Scholar
  8. Choi SH, Kim SM, Oh JT, Park JY, Seo JM, Lee SK. Solid pseudopapillary tumor of the pancreas: a multicenter study of 23 pediatric cases. J Pediatr Surg. 2006;41(12):1992–5.PubMedView ArticleGoogle Scholar
  9. van den Akker M, Angelini P, Taylor G, Chami R, Gerstle JT, Gupta A. Malignant pancreatic tumors in children: a single-institution series. J Pediatr Surg. 2012;47(4):681–7.PubMedView ArticleGoogle Scholar

Copyright

© Bidassek et al. 2016

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