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Y. Okubo, T. Yokose, M. Tuchiya, A. Mitua, M. Wakayama, C. Hasegawa, D. Sasai, T. Nemoto and K. Shibuya, “Duodenal Gangliocytic Paraganglioma Showing Lymph Node Metastasis: a Rare Case Report,” Diagnostic Pathology, Vol. 5, 2010, p. 27. doi:10.1186/1746-1596-5-27

has been cited by the following article:

• TITLE: A Rare Cause of Melaena-Duodenal Gangliocytic Paraganglioma

  AUTHORS: Carmencita Esquivel, Suresh Navadgi, Greg Otto, Rebecca Thomas

  KEYWORDS: Melaena; Rare Tumour; Neuroendocrine Tumour; Diagnostic Histological Triad; Gangliocytic Paraganglioma

  JOURNAL NAME: Surgical Science, Vol.3 No.4, April 24, 2012

  ABSTRACT: Gangliocytic paraganglioma (GP), a rare tumour that arises most frequently from the periampullary area, is considered to be a benign neoplasm with a potential for lymphatic spread. Distant metastases are rare [1]. We report a case of a 51 year old female who presented with abdominal pain, anaemia and melaena. Endoscopy, push enteroscopy and biopsy revealed a periampullary neuroendocrine tumour. Immunohistochemistry of the pancreatic duodenectomy specimen demonstrated a duodenal gangliocytic paraganglioma with no lymph node metastases. We review the literature on this rare tumour and the current treatment protocol.