An autopsy case of alpha-fetoprotein-producing large duodenal adenocarcinoma
We report an autopsy case of a large duodenal adenocarcinoma that produced alpha-fetoprotein (AFP). The patient was a man in his 70s with diabetes mellitus. He presented with epigastralgia and was referred to our hospital. Upper gastrointestinal endoscopy and abdominal computed tomography revealed a...
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Veröffentlicht in: | Clinical journal of gastroenterology 2023-12, Vol.16 (6), p.829-835 |
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creator | Hirota, Sumire Naganuma, Atsushi Kobayashi, Rintaro Suzuki, Yuhei Hoshino, Takashi Yasuoka, Hidetoshi Tanaka, Yuko Uraoka, Toshio Kakizaki, Satoru |
description | We report an autopsy case of a large duodenal adenocarcinoma that produced alpha-fetoprotein (AFP). The patient was a man in his 70s with diabetes mellitus. He presented with epigastralgia and was referred to our hospital. Upper gastrointestinal endoscopy and abdominal computed tomography revealed a large tumor of 11 cm in diameter in the descending limb of the duodenum. A tumor biopsy showed poorly differentiated adenocarcinoma. Although his carcinoembryonic antigen (CEA) and carbohydrate antigen 19–9 (CA19-9) levels were within the normal range, his AFP levels were significantly elevated (42,078.4 ng/mL). Due to vascular invasion, curative resection was not feasible, and chemotherapy was chosen as the treatment option. After gastrojejunostomy was performed to enable oral intake, one cycle of modified leucovorin/5-fluorouracil/oxaliplatin (mFOLFOX6) therapy was administered. However, it proved ineffective, and the patient's anorexia gradually worsened. Ultimately, he succumbed to the progression of cancer cachexia. Autopsy findings revealed a 14-cm-long duodenal carcinoma primarily located in the duodenal bulb, with direct invasion into the stomach, pancreas, and liver. A pathological examination confirmed a diagnosis of poorly differentiated adenocarcinoma with AFP production. Duodenal cancer is rare, and AFP-producing duodenal cancer is even rarer, with only 21 reported cases, including our own. We present this autopsy case of AFP-producing duodenal adenocarcinoma and review the cases reported in the relevant literature. |
doi_str_mv | 10.1007/s12328-023-01843-5 |
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The patient was a man in his 70s with diabetes mellitus. He presented with epigastralgia and was referred to our hospital. Upper gastrointestinal endoscopy and abdominal computed tomography revealed a large tumor of 11 cm in diameter in the descending limb of the duodenum. A tumor biopsy showed poorly differentiated adenocarcinoma. Although his carcinoembryonic antigen (CEA) and carbohydrate antigen 19–9 (CA19-9) levels were within the normal range, his AFP levels were significantly elevated (42,078.4 ng/mL). Due to vascular invasion, curative resection was not feasible, and chemotherapy was chosen as the treatment option. After gastrojejunostomy was performed to enable oral intake, one cycle of modified leucovorin/5-fluorouracil/oxaliplatin (mFOLFOX6) therapy was administered. However, it proved ineffective, and the patient's anorexia gradually worsened. Ultimately, he succumbed to the progression of cancer cachexia. Autopsy findings revealed a 14-cm-long duodenal carcinoma primarily located in the duodenal bulb, with direct invasion into the stomach, pancreas, and liver. A pathological examination confirmed a diagnosis of poorly differentiated adenocarcinoma with AFP production. Duodenal cancer is rare, and AFP-producing duodenal cancer is even rarer, with only 21 reported cases, including our own. We present this autopsy case of AFP-producing duodenal adenocarcinoma and review the cases reported in the relevant literature.</description><identifier>ISSN: 1865-7257</identifier><identifier>EISSN: 1865-7265</identifier><identifier>DOI: 10.1007/s12328-023-01843-5</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Abdominal Surgery ; Case Report ; Colorectal Surgery ; Gastroenterology ; Hepatology ; Medicine ; Medicine & Public Health ; Surgical Oncology</subject><ispartof>Clinical journal of gastroenterology, 2023-12, Vol.16 (6), p.829-835</ispartof><rights>Japanese Society of Gastroenterology 2023. 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The patient was a man in his 70s with diabetes mellitus. He presented with epigastralgia and was referred to our hospital. Upper gastrointestinal endoscopy and abdominal computed tomography revealed a large tumor of 11 cm in diameter in the descending limb of the duodenum. A tumor biopsy showed poorly differentiated adenocarcinoma. Although his carcinoembryonic antigen (CEA) and carbohydrate antigen 19–9 (CA19-9) levels were within the normal range, his AFP levels were significantly elevated (42,078.4 ng/mL). Due to vascular invasion, curative resection was not feasible, and chemotherapy was chosen as the treatment option. After gastrojejunostomy was performed to enable oral intake, one cycle of modified leucovorin/5-fluorouracil/oxaliplatin (mFOLFOX6) therapy was administered. However, it proved ineffective, and the patient's anorexia gradually worsened. Ultimately, he succumbed to the progression of cancer cachexia. Autopsy findings revealed a 14-cm-long duodenal carcinoma primarily located in the duodenal bulb, with direct invasion into the stomach, pancreas, and liver. A pathological examination confirmed a diagnosis of poorly differentiated adenocarcinoma with AFP production. Duodenal cancer is rare, and AFP-producing duodenal cancer is even rarer, with only 21 reported cases, including our own. We present this autopsy case of AFP-producing duodenal adenocarcinoma and review the cases reported in the relevant literature.</description><subject>Abdominal Surgery</subject><subject>Case Report</subject><subject>Colorectal Surgery</subject><subject>Gastroenterology</subject><subject>Hepatology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Surgical Oncology</subject><issn>1865-7257</issn><issn>1865-7265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kD1PwzAQhi0EEqXwB5gyshjOX7EzVhVfUiUWmK2r7ZRUaVzsZOi_x6WIkek93b3v6e4h5JbBPQPQD5lxwQ0FLigwIwVVZ2TGTK2o5rU6_6uVviRXOW8Bag5azMhqMVQ4jXGfD5XDHKrYVtjvP5G2oXRTHEM30KJ-ct2wqXpMm1D5KfowYF9hkegwlVnc4TW5aLHP4eZX5-Tj6fF9-UJXb8-vy8WKOsHlSLnyHiRfyyCghcCFdKaVwXtjwloz3XhsgjLcrUG3TJnSgrpB5EwywFqLObk77S13fU0hj3bXZRf6HocQp2y5UaKRNYAqVn6yuhRzTqG1-9TtMB0sA3tEZ0_obEFnf9DZY0icQrmYh01IdhunVP7N_6W-AcBScY8</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Hirota, Sumire</creator><creator>Naganuma, Atsushi</creator><creator>Kobayashi, Rintaro</creator><creator>Suzuki, Yuhei</creator><creator>Hoshino, Takashi</creator><creator>Yasuoka, Hidetoshi</creator><creator>Tanaka, Yuko</creator><creator>Uraoka, Toshio</creator><creator>Kakizaki, Satoru</creator><general>Springer Nature Singapore</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0224-7093</orcidid></search><sort><creationdate>20231201</creationdate><title>An autopsy case of alpha-fetoprotein-producing large duodenal adenocarcinoma</title><author>Hirota, Sumire ; Naganuma, Atsushi ; Kobayashi, Rintaro ; Suzuki, Yuhei ; Hoshino, Takashi ; Yasuoka, Hidetoshi ; Tanaka, Yuko ; Uraoka, Toshio ; Kakizaki, Satoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c324t-25dd042b4e30f0e234c8f4edd88eb7179da9e582cb07f158717069aa21410a673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abdominal Surgery</topic><topic>Case Report</topic><topic>Colorectal Surgery</topic><topic>Gastroenterology</topic><topic>Hepatology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Surgical Oncology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hirota, Sumire</creatorcontrib><creatorcontrib>Naganuma, Atsushi</creatorcontrib><creatorcontrib>Kobayashi, Rintaro</creatorcontrib><creatorcontrib>Suzuki, Yuhei</creatorcontrib><creatorcontrib>Hoshino, Takashi</creatorcontrib><creatorcontrib>Yasuoka, Hidetoshi</creatorcontrib><creatorcontrib>Tanaka, Yuko</creatorcontrib><creatorcontrib>Uraoka, Toshio</creatorcontrib><creatorcontrib>Kakizaki, Satoru</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hirota, Sumire</au><au>Naganuma, Atsushi</au><au>Kobayashi, Rintaro</au><au>Suzuki, Yuhei</au><au>Hoshino, Takashi</au><au>Yasuoka, Hidetoshi</au><au>Tanaka, Yuko</au><au>Uraoka, Toshio</au><au>Kakizaki, Satoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An autopsy case of alpha-fetoprotein-producing large duodenal adenocarcinoma</atitle><jtitle>Clinical journal of gastroenterology</jtitle><stitle>Clin J Gastroenterol</stitle><date>2023-12-01</date><risdate>2023</risdate><volume>16</volume><issue>6</issue><spage>829</spage><epage>835</epage><pages>829-835</pages><issn>1865-7257</issn><eissn>1865-7265</eissn><abstract>We report an autopsy case of a large duodenal adenocarcinoma that produced alpha-fetoprotein (AFP). The patient was a man in his 70s with diabetes mellitus. He presented with epigastralgia and was referred to our hospital. Upper gastrointestinal endoscopy and abdominal computed tomography revealed a large tumor of 11 cm in diameter in the descending limb of the duodenum. A tumor biopsy showed poorly differentiated adenocarcinoma. Although his carcinoembryonic antigen (CEA) and carbohydrate antigen 19–9 (CA19-9) levels were within the normal range, his AFP levels were significantly elevated (42,078.4 ng/mL). Due to vascular invasion, curative resection was not feasible, and chemotherapy was chosen as the treatment option. After gastrojejunostomy was performed to enable oral intake, one cycle of modified leucovorin/5-fluorouracil/oxaliplatin (mFOLFOX6) therapy was administered. However, it proved ineffective, and the patient's anorexia gradually worsened. Ultimately, he succumbed to the progression of cancer cachexia. Autopsy findings revealed a 14-cm-long duodenal carcinoma primarily located in the duodenal bulb, with direct invasion into the stomach, pancreas, and liver. A pathological examination confirmed a diagnosis of poorly differentiated adenocarcinoma with AFP production. Duodenal cancer is rare, and AFP-producing duodenal cancer is even rarer, with only 21 reported cases, including our own. We present this autopsy case of AFP-producing duodenal adenocarcinoma and review the cases reported in the relevant literature.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><doi>10.1007/s12328-023-01843-5</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-0224-7093</orcidid></addata></record> |
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title | An autopsy case of alpha-fetoprotein-producing large duodenal adenocarcinoma |
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