TY - JOUR
T1 - Signet-ring cell carcinoma of the ampulla of Vater
T2 - Report of a case
AU - Akatsu, Tomotaka
AU - Aiura, Koichi
AU - Takahashi, Shin
AU - Kameyama, Kaori
AU - Kitajima, Masaki
AU - Kitagawa, Yuko
PY - 2007/12/1
Y1 - 2007/12/1
N2 - Signet-ring cell carcinoma (SRCC) of the ampulla of Vater is uncommon, and only 13 cases have been previously described. We herein report a rare case of a 43-year-old woman with SRCC in the ampulla of Vater. Although this histologic type of cancer generally predicts a poor prognosis elsewhere in the gastrointestinal tract, the present patient has survived with no evidence of recurrence for 7.5 years. The patient was hospitalized for pruritus and jaundice. She underwent a pancreaticoduodenectomy with an extended lymphadenectomy for ampullary carcinoma. This neoplasm was classified as AcdbBi, 2.0 × 1.8 cm, ulcerative type, Panc0, Du2, T 2N0M(-), Stage II according to the Japanese Classification on Cancer of the Biliary Tract. Unfortunately, previous reports of ampullary SRCC have been limited to short-term follow-ups with a median period of only 12 months (range, 6-134 months), and long-term survival (more than 5 years) was only documented in two cases without lymph node metastasis (including the present case). In conclusion, the experience gained in the present and previous cases suggests that long-term survival is possible following a curative resection in selected patients with ampullary SRCC without nodal involvement. Due to the lack of sufficient evidence, additional reports are warranted to determine whether SRCC also portends a poor prognosis in patients with ampullary cancer.
AB - Signet-ring cell carcinoma (SRCC) of the ampulla of Vater is uncommon, and only 13 cases have been previously described. We herein report a rare case of a 43-year-old woman with SRCC in the ampulla of Vater. Although this histologic type of cancer generally predicts a poor prognosis elsewhere in the gastrointestinal tract, the present patient has survived with no evidence of recurrence for 7.5 years. The patient was hospitalized for pruritus and jaundice. She underwent a pancreaticoduodenectomy with an extended lymphadenectomy for ampullary carcinoma. This neoplasm was classified as AcdbBi, 2.0 × 1.8 cm, ulcerative type, Panc0, Du2, T 2N0M(-), Stage II according to the Japanese Classification on Cancer of the Biliary Tract. Unfortunately, previous reports of ampullary SRCC have been limited to short-term follow-ups with a median period of only 12 months (range, 6-134 months), and long-term survival (more than 5 years) was only documented in two cases without lymph node metastasis (including the present case). In conclusion, the experience gained in the present and previous cases suggests that long-term survival is possible following a curative resection in selected patients with ampullary SRCC without nodal involvement. Due to the lack of sufficient evidence, additional reports are warranted to determine whether SRCC also portends a poor prognosis in patients with ampullary cancer.
KW - Ampulla of Vater
KW - Long-term survival
KW - Signet-ring cell carcinoma
UR - http://www.scopus.com/inward/record.url?scp=36448981793&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=36448981793&partnerID=8YFLogxK
U2 - 10.1007/s00595-007-3534-4
DO - 10.1007/s00595-007-3534-4
M3 - Article
C2 - 18030577
AN - SCOPUS:36448981793
SN - 0941-1291
VL - 37
SP - 1110
EP - 1114
JO - Surgery Today
JF - Surgery Today
IS - 12
ER -