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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/09/02 16:46:39」(JST)

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1. 小腸腫瘍の疫学、臨床的特徴、および種類 epidemiology clinical features and types of small bowel neoplasms
2. 傍神経節腫および褐色細胞腫：悪性疾患のマネージメント paraganglioma and pheochromocytoma management of malignant disease
3. 頭部および頚部の傍神経節腫 paragangliomas of the head and neck
4. 胸腺神経内分泌（カルチノイド）腫瘍 thymic neuroendocrine carcinoid tumors
5. 小児における褐色細胞腫 pheochromocytoma in children

Manjaly JG1, Alexander VR2, Pepper CM2, Ifeacho SN2, Hewitt RJ2, Hartley BE2.
International journal of pediatric otorhinolaryngology.Int J Pediatr Otorhinolaryngol.2015 Jul;79(7):1007-12. doi: 10.1016/j.ijporl.2015.04.012. Epub 2015 Apr 22.
OBJECTIVES: Ganglioneuroblastomas represent a histological subgroup of the rare neuroblastic tumours with intermediate malignant potential arising from neural crest progenitor cells of sympathetic nerves. Diagnosis can often be difficult based on imaging alone. We describe 4 cases of children presen
PMID 25921075

Wing LA1, Conaglen JV1,2, Meyer-Rochow GY3,2, Elston MS1,2.
The Journal of clinical endocrinology and metabolism.J Clin Endocrinol Metab.2015 Jun 17:jc20152122. [Epub ahead of print]
CONTEXT: Pregnancies complicated by a phaeochromocytoma or paraganglioma are very rare, being estimated to occur in 0.007% of all pregnancies. Both the wellbeing of the mother and fetus need to be considered, and management can be challenging. The optimal management of women with a phaeochromocytoma
PMID 26083822

Gangliocytic Paraganglioma With Atypical Immunohistochemical Features Presenting as Extrahepatic Biliary Obstruction.

Sharma S1, Gaspar BL1, Kumar P1, Yadav TD1, Vasishta RK2.
International journal of surgical pathology.Int J Surg Pathol.2015 Jun 16. pii: 1066896915589969. [Epub ahead of print]
Gangliocytic paraganglioma is a rare benign tumor of upper gastrointestinal tract that most commonly involves the second part of duodenum. The tumor is detected incidentally on imaging in most of the cases. However, presentation with extrahepatic biliary obstruction is extremely rare. We recently en
PMID 26081293