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Azagoh-Kouadio, R., Couitchéré, L.G., Kouyaté, M., Atteby, J.-J.Y., Enoh, J.S., Cissé, L. and Oulai, S. (2018) Tumeur pancréatique rare de découverte fortuite chez un enfant en Côte d’Ivoire. Pan African Medical Journal, 29, Article 171.
https://doi.org/10.11604/pamj.2018.29.171.12392

has been cited by the following article:

• TITLE: Solid-Pseudopapillary Tumor: Case Report and Literature Review

  AUTHORS: Nomenjanahary Lalaina, Rabarison Manoahasina Ranaliarinosy, Razafimahefa Vahatra Joëlle, Randrianjafisamindrakotroka Nantenaina Soa

  KEYWORDS: Pancreas, Tumor, Solid-Pseudopapillary, Frantz, Antananarivo

  JOURNAL NAME: Open Journal of Pathology, Vol.14 No.1, December 12, 2023

  ABSTRACT: Solid-pseudopapillary tumor of the pancreas (SPT) or Frantz’s tumor is a rare epithelial neoplasm that represents 0.3% to 2.7% of exocrine pancreatic tumors. These tumors occur mainly in young women and have a good prognosis. We present a case of a 19-year-old female patient who presented to the emergency for abdominal pain. Physical examination reveals a left hypochondrium mass. Ultrasound imaging showed an encapsulated caudal pancreatic mass with cystic components. The patient underwent tumor excision and lymph node removal. Macroscopically, the tumor was encapsulated and measuring 12 × 8 × 7 cm. It has a solid-cystic and hemorrhagic appearance inside. Histologically, the tumor had two components: solid and papillary. Tumor tissue showed monomorphic tumor cells radiating around blood vessels. Perineural invasion and vascular emboli were not seen. Three lymph nodes without metastases were observed. The diagnosis of solid-pseudopapillary tumor of the pancreas (SPT) or Frantz’s tumor was retained. Solid-pseudo-papillary tumor of the pancreas is rare and not always suspected by the physician. The clinical and imaging patterns are not specific. Anatomopathological examination confirmed the diagnosis. The patient underwent curative surgery.