scholarly journals Gastric Mixed Adenoneuroendocrine Carcinoma with Revised Diagnosis after Retrospective Pathologic Review

Author(s):  
Bo Seok Jeong ◽  
Hye Won Hwang ◽  
Jong Won Kim ◽  
In Gyu Hwang ◽  
Jae Yong Park
2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Hiromi Nagata ◽  
Hironori Tsujimoto ◽  
Yoshihisa Yaguchi ◽  
Keita Kouzu ◽  
Yujiro Itazaki ◽  
...  

Abstract Background Trastuzumab (T-mab)-based chemotherapy is a standard regimen for human epithelial growth factor 2 (HER2)-positive gastric cancer. However, some patients have demonstrated a change in HER2 status after T-mab-based treatment of breast cancer. We report a rare case of mixed adenoneuroendocrine carcinoma with loss of HER2 positivity after T-mab-based chemotherapy for HER2-positive gastric cancer. Case presentation A 60-year-old man presented with a mass of the upper abdomen, which was diagnosed as adenocarcinoma with a HER2 score of 3+ by endoscopic biopsy. He received seven cycles of combination chemotherapy with capecitabine, cisplatin, and T-mab. Subsequently, he underwent open total gastrectomy, distal pancreatosplenectomy, and extended left hepatic lobectomy as a conversion surgery. The surgically resected specimen demonstrated both adenocarcinoma and neuroendocrine components; therefore, it was diagnosed as HER2-negative mixed adenoneuroendocrine carcinoma. Although the patient received additional chemotherapy, multiple liver metastases appeared at 3 months postoperatively and he died at 6 months postoperatively because of the rapidly progressing metastatic tumor. Conclusions We encountered a rare case of rapidly progressive mixed adenoneuroendocrine carcinoma that was negative for HER2 expression after T-mab treatment combined with chemotherapy.


2021 ◽  
Author(s):  
Alessandro Iacomino ◽  
Ugo Grossi ◽  
Stefano Doratiotto ◽  
Alberto Brun Peressut ◽  
Patrizia Pelizzo ◽  
...  

Author(s):  
Khalil Issa ◽  
Blaine D. Smith ◽  
Samantha J. Kaplan ◽  
John Madden ◽  
David W. Jang ◽  
...  

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Sulai Liu ◽  
Zhendong Zhong ◽  
Meng Xiao ◽  
Yinghui Song ◽  
Youye Zhu ◽  
...  

Abstract Background The World Health Organization's updated classification of digestive system neuroendocrine tumors in 2010 first proposed the classification of mixed adenoneuroendocrine carcinoma (MANEC). The incidence of biliary malignant tumors with neuroendocrine tumors accounts for less than 1% of all neuroendocrine tumors. Moreover, the incidence of hilar bile duct with MANEC is very rare. Case presentation A 65-year-old female patient came to our hospital for repeated abdominal pain for more than 4 months and skin sclera yellow staining for 1 week. Contrast-enhanced computed tomography imaging and magnetic resonance results suggested a hilar tumor for Bismuth-Corlette Type II. The patient underwent radical surgery for hilar cholangiocarcinoma. Finally, the patient was diagnosed with hilar bile duct MANEC, staged 1 (pT1N0M0) based on the eighth edition of the AJCC. Histopathology showed that the tumor was a biliary tumor with both adenocarcinoma and neuroendocrine carcinoma. No evidence of recurrence and metastasis after 20 months of follow-up. Conclusions We first reported a MANEC that originated in the hilar bile duct. As far as we known, there were few reports of biliary MANEC, and the overall prognosis was poor. We also found that the higher the Ki-67 index, the worse the prognosis of this type of patient. Radical surgery is the most effective treatment.


2018 ◽  
Vol 73 ◽  
pp. 184-191 ◽  
Author(s):  
Shayna A. Brathwaite ◽  
Stephen M. Smith ◽  
Lai Wai ◽  
Wendy Frankel ◽  
John Hays ◽  
...  

2018 ◽  
Vol 96 (1) ◽  
pp. 58-61
Author(s):  
Divaldo Monteiro de Melo Santos ◽  
Eudaldo López-Tomassetti Fernández ◽  
Miguel Sánchez Ramos ◽  
Juan Ramón Hernández Hernández

2017 ◽  
Vol 152 (5) ◽  
pp. S1287
Author(s):  
Bernardo Borraez ◽  
Jaime A. Montoya ◽  
Oscar A. Guevara ◽  
Ricardo Oliveros ◽  
Raul Pinilla

2021 ◽  
Vol 11 (1) ◽  
pp. 1891-1894
Author(s):  
Irene Thomas ◽  
Divya Surendran ◽  
Joy Augustine

Mixed adenoneuroendocrine carcinoma is a rare neoplasm with both epithelial and neuroendocrine components. To date, only a few cases of this neoplasm have been reported in the literature among which gastric mixed adenoneuroendocrine carcinoma is very rare. We are reporting a case of gastric mixed adenoneuroendocrine carcinoma with squamous cell differentiation. Histopathological features, biological behaviour and the treatment of this rare tumour type have been discussed briefly.


2019 ◽  
Vol 80 (7) ◽  
pp. 1303-1308
Author(s):  
Shu ICHIMIYA ◽  
Jiro OHUCHIDA ◽  
Shinsuke KUBO ◽  
Soshi TERASAKA ◽  
Yuji UEDA ◽  
...  

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