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Table 1 Characteristics in reported cases of gastroenteropancreatic neuroendocrine tumors of the accessory papilla of the duodenum

From: Gastroenteropancreatic neuroendocrine tumor of the accessory papilla of the duodenum: a case report

Reports (year)

Age/sex

Symptom

Size (mm)

Treatment

Pathology

Outcome

Malone et al. (1985) [3]

46/M

Abdominal pain

Anorexia

Steatorrhea

Wight loss

5–7.5

Local excision (Surgically)

Somatostatinoma

No recurrence, 16 months

Borobia et al. (2001) [4]

46/F

Diarrhea

Steatorrhea

NA

Local excision (Surgically)

Neuroendocrine tumor

No recurrence, 3 years

Singh et al. (2003) [5]

35/F

Pancreatitis

10

Local excision

Sphincteroplasty (surgically)

Carcinoid

Negative margin

No recurrence, 6 months

Wang et al. (2005) [6]

50/M

Multiple melenas

Polycythemia vera

9

Local excision (surgically)

Carcinoid

No recurrence, 3 years

Itoi et al. (2007) [7]

65/M

No

12

Local excision (endoscopically)

Invasive carcinoid tumor

Positive margin

No recurrence, 4 years

Stömmer et al. (1987) [8]

56/F

Jaundice

Wight loss

3

PD

Somatostatinoma

No LNM

NA

Lowes et al. (1988) [9]

50/F

Abdominal pain

Diarrhea

Wight loss

12

PD

Somatostatinoma

LNM (regional areas)

NA

Waisberg et al. (2006) [10]

57/F

Abdominal pain

Diarrhea

Weight loss

27

PD

Carcinoid (somatostatinoma)

LNM (regional areas)

Death, POD 21

Kim et al. (2010) [11]

56/F

Abdominal pain

12

PD

Carcinoid

Vascular invasion

No perineural invasion

LNM (regional areas)

NA

Our case

70/M

No

8

Robotic PD

Neuroendocrine tumor

Well-differentiated (G1)

No lymphovascular invasion

LNM (regional areas)

No recurrence, 6 months

  1. M male, F female, PD pancreatoduodenectomy, LNM lymph node metastasis, NA not available