CC BY-NC-ND 4.0 · Endosc Int Open 2020; 08(01): E25-E28
DOI: 10.1055/a-1038-3852
Case report
Owner and Copyright © Georg Thieme Verlag KG 2020

A rare case of perivascular epithelioid cell tumor (PEComa) of the pancreas diagnosed by endoscopic ultrasound

J. D. Ulrich
1   Klinik und Poliklinik für Innere Medizin II, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany
,
K. Specht
2   Institut für Allgemeine Pathologie und Pathologische Anatomie, Technische Universität München, Munich, Germany
,
A. M. Schlitter
2   Institut für Allgemeine Pathologie und Pathologische Anatomie, Technische Universität München, Munich, Germany
,
G. O. Ceyhan
3   Klinik und Poliklinik für Chirurgie, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany
,
M. Quante
1   Klinik und Poliklinik für Innere Medizin II, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany
,
R. M. Schmid
1   Klinik und Poliklinik für Innere Medizin II, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany
,
C. Schlag
1   Klinik und Poliklinik für Innere Medizin II, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany
› Author Affiliations
Further Information

Publication History

submitted 04 January 2019

accepted after revision 08 July 2019

Publication Date:
08 January 2020 (online)

Abstract

A 49-year-old woman consulted her general practitioner (GP) regarding epigastric pain that she had experienced for 2 months. Physical examination and laboratory results were unremarkable. An abdominal ultrasound indicated a solid pancreatic tumor, which was confirmed on subsequent CT and MRI. Endoscopic ultrasound (EUS) showed a well-defined heterogeneous, predominantly hypoechoic mass in the pancreatic body, so a neuroendocrine tumor (NET) was suspected. However, EUS-guided fine-needle aspiration (EUS-FNA) was performed and based on (immuno-)histochemical findings, the extremely rare diagnosis of a perivascular epithelioid cell tumor (PEComa) of the pancreas was made. Due to the malignant potential of pancreatic PEComas, laparoscopic left-sided pancreatectomy was performed. We present a case diagnosed by preoperative EUS-FNA highlighting the clinical and endosonographic features which help to distinguish it from its most important differential diagnosis, neuroendocrine tumors (NETs) of the pancreas.

 
  • References

  • 1 Bonetti F, Pea M, Martignoni G. et al. PEC and sugar. Am J Surg Pathol 1992; 16: 307-308
  • 2 Zamboni G, Pea M, Martignoni G. et al. Clear cell “sugar” tumor of the pancreas: A novel member of the family of lesions characterized by the presence of perivascular epithelioid cells. Am J Surg Pathol 1996; 20: 722-730
  • 3 Fletcher CDM, Bridge JA, Hogendoorn P. et al. WHO classification of tumours of soft tissue and bone. 4th. edn. Geneva: WHO; 2013
  • 4 Zhang S, Chen F, Huang X. et al. Perivascular epithelial cell tumor (PEComa) of the pancreas: A case report and review of literature. Medicine 2017; 96: e7050
  • 5 Giusti M, Sidoti M, Augeri C. et al. Effect of short-term treatment with low dosages of the proton-pump inhibitor omeprazole on serum chromogranin A levels in man. Eur J Endocrinol 2004; 150: 299-303
  • 6 Tirumani SH, Shinagare AB, Hargreaves J. et al. Imaging features of primary and metastatic malignant perivascular epithelioid cell tumors. Am J Roentgenol 2014; 202: 252-258
  • 7 Öberg K, Knigge U, Kwekkeboom D. et al. Neuroendocrine gastro-entero-pancreatic tumors: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2012; 23: vii124-vii130
  • 8 Collins K, Buckley T, Anderson K. et al. Perivascular epithelioid cell tumor (PEComa) of pancreas diagnosed preoperatively by endoscopic ultrasound-guided fine-needle aspiration: A case report and review of literature. Diagn Cytopathol 2017; 45: 59-65
  • 9 Hartley CP, Kwiatkowski DJ, Hamieh L. et al. Pancreatic PEComa is a novel member of the family of tuberous sclerosis complex-associated tumors: case report and review of the literature. Virchows Archiv 2016; 469: 707-710