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Neuroendocrine Carcinoma of the Extrahepatic Bile Ducts: A Case Report
Patient: Female, 42-year-old Final Diagnosis: Biliary neuroendocrine carcinoma involving the common hepatic duct • common bile duct and cystic duct PT1N0M0G3R0 Symptoms: Itching of the hands, forearms and lower legs, followed by symptoms of obstructive jaundice Clinical Procedure: Cholecystectomy •...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290433/ https://www.ncbi.nlm.nih.gov/pubmed/37340629 http://dx.doi.org/10.12659/AJCR.939239 |
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author | Jevdokimov, Denis Tauvena, Elina Jevdokimova, Natalija Vilisova, Sofija Kriviča, Olga Briede, Inese Tone, Tatjana Staka, Aiga Gerina-Berzina, Aija Ozolins, Arturs Pukitis, Aldis |
author_facet | Jevdokimov, Denis Tauvena, Elina Jevdokimova, Natalija Vilisova, Sofija Kriviča, Olga Briede, Inese Tone, Tatjana Staka, Aiga Gerina-Berzina, Aija Ozolins, Arturs Pukitis, Aldis |
author_sort | Jevdokimov, Denis |
collection | PubMed |
description | Patient: Female, 42-year-old Final Diagnosis: Biliary neuroendocrine carcinoma involving the common hepatic duct • common bile duct and cystic duct PT1N0M0G3R0 Symptoms: Itching of the hands, forearms and lower legs, followed by symptoms of obstructive jaundice Clinical Procedure: Cholecystectomy • ERCP • resection of a hepatobiliary mass Specialty: Gastroenterology and Hepatology • Oncology • Pathology • Surgery OBJECTIVE: Rare disease BACKGROUND: Neuroendocrine tumors (NETs) primarily originating from the extrahepatic biliary (EB) tree are a medical rarity, accounting for less than 100 recorded instances globally. This case report outlines an encounter with this uncommon condition, demonstrating the complexities of diagnosis and management. CASE REPORT: A 42-year-old woman presented at our Emergency Department with a 3-week history of itching and symptoms of obstructive jaundice. Initial laboratory tests showed hyperbilirubinemia and elevated liver transaminases. Abdominal ultrasonography indicated choledocholithiasis. Magnetic resonance imaging suggested either Mirizzi syndrome or a proximal common bile duct neoplasm. Abdominal computed tomography showed cholestasis, suggesting choledocholithiasis or cholangiocarcinoma (type-1). An endoscopic retrograde cholangiopancreatography with biliary and pancreatic duct stenting was performed for drainage, with brush cytology confirming adenocarcinoma. The patient was referred for surgical resection of the bile duct tumor, involving extrahepatic bile duct resection, en bloc cholecystectomy, lymphadenectomy, Roux-en-Y anastomosis, and biliary drainage. Histopathology identified a neuroendocrine carcinoma. Following surgery, the patient underwent eight cycles of FOLFOX6 chemotherapy, with no disease relapse post-treatment. CONCLUSIONS: This case emphasizes multidisciplinary teamwork importance in managing rare diseases like EB bile duct NETs. These tumors’ rarity and symptom ambiguity necessitate histological examination for accurate diagnosis. This report aims to guide healthcare professionals facing similar future cases. |
format | Online Article Text |
id | pubmed-10290433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102904332023-06-25 Neuroendocrine Carcinoma of the Extrahepatic Bile Ducts: A Case Report Jevdokimov, Denis Tauvena, Elina Jevdokimova, Natalija Vilisova, Sofija Kriviča, Olga Briede, Inese Tone, Tatjana Staka, Aiga Gerina-Berzina, Aija Ozolins, Arturs Pukitis, Aldis Am J Case Rep Articles Patient: Female, 42-year-old Final Diagnosis: Biliary neuroendocrine carcinoma involving the common hepatic duct • common bile duct and cystic duct PT1N0M0G3R0 Symptoms: Itching of the hands, forearms and lower legs, followed by symptoms of obstructive jaundice Clinical Procedure: Cholecystectomy • ERCP • resection of a hepatobiliary mass Specialty: Gastroenterology and Hepatology • Oncology • Pathology • Surgery OBJECTIVE: Rare disease BACKGROUND: Neuroendocrine tumors (NETs) primarily originating from the extrahepatic biliary (EB) tree are a medical rarity, accounting for less than 100 recorded instances globally. This case report outlines an encounter with this uncommon condition, demonstrating the complexities of diagnosis and management. CASE REPORT: A 42-year-old woman presented at our Emergency Department with a 3-week history of itching and symptoms of obstructive jaundice. Initial laboratory tests showed hyperbilirubinemia and elevated liver transaminases. Abdominal ultrasonography indicated choledocholithiasis. Magnetic resonance imaging suggested either Mirizzi syndrome or a proximal common bile duct neoplasm. Abdominal computed tomography showed cholestasis, suggesting choledocholithiasis or cholangiocarcinoma (type-1). An endoscopic retrograde cholangiopancreatography with biliary and pancreatic duct stenting was performed for drainage, with brush cytology confirming adenocarcinoma. The patient was referred for surgical resection of the bile duct tumor, involving extrahepatic bile duct resection, en bloc cholecystectomy, lymphadenectomy, Roux-en-Y anastomosis, and biliary drainage. Histopathology identified a neuroendocrine carcinoma. Following surgery, the patient underwent eight cycles of FOLFOX6 chemotherapy, with no disease relapse post-treatment. CONCLUSIONS: This case emphasizes multidisciplinary teamwork importance in managing rare diseases like EB bile duct NETs. These tumors’ rarity and symptom ambiguity necessitate histological examination for accurate diagnosis. This report aims to guide healthcare professionals facing similar future cases. International Scientific Literature, Inc. 2023-06-21 /pmc/articles/PMC10290433/ /pubmed/37340629 http://dx.doi.org/10.12659/AJCR.939239 Text en © Am J Case Rep, 2023 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Jevdokimov, Denis Tauvena, Elina Jevdokimova, Natalija Vilisova, Sofija Kriviča, Olga Briede, Inese Tone, Tatjana Staka, Aiga Gerina-Berzina, Aija Ozolins, Arturs Pukitis, Aldis Neuroendocrine Carcinoma of the Extrahepatic Bile Ducts: A Case Report |
title | Neuroendocrine Carcinoma of the Extrahepatic Bile Ducts: A Case Report |
title_full | Neuroendocrine Carcinoma of the Extrahepatic Bile Ducts: A Case Report |
title_fullStr | Neuroendocrine Carcinoma of the Extrahepatic Bile Ducts: A Case Report |
title_full_unstemmed | Neuroendocrine Carcinoma of the Extrahepatic Bile Ducts: A Case Report |
title_short | Neuroendocrine Carcinoma of the Extrahepatic Bile Ducts: A Case Report |
title_sort | neuroendocrine carcinoma of the extrahepatic bile ducts: a case report |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290433/ https://www.ncbi.nlm.nih.gov/pubmed/37340629 http://dx.doi.org/10.12659/AJCR.939239 |
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