Large-Cell Esophageal Neuroendocrine Tumor Leading to Hepatorenal Syndrome
Neuroendocrine tumors are tumors that arise from the enterochromaffin cells in the neuroendocrine tissue found throughout the body, particularly the digestive tract, pancreas, and thymus. Neuroendocrine tumors of the esophagus are extremely rare and highly aggressive in nature. We present the case o...
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Published in | Curēus (Palo Alto, CA) Vol. 14; no. 4; p. e23720 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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United States
Springer Nature B.V
01.04.2022
Cureus |
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Abstract | Neuroendocrine tumors are tumors that arise from the enterochromaffin cells in the neuroendocrine tissue found throughout the body, particularly the digestive tract, pancreas, and thymus. Neuroendocrine tumors of the esophagus are extremely rare and highly aggressive in nature. We present the case of a 55-year-old Hispanic male who initially presented to the emergency department with right-sided abdominal pain. Imaging revealed innumerable lesions occupying half of the liver parenchyma. Subsequent endoscopy with biopsy of the esophageal and liver lesions along with immunohistochemistry staining was suggestive of a large cell neuroendocrine tumor. He later presented with generalized weakness and right-sided abdominal pain with worsening hepatic and renal function. Over the course of the patient's stay in the hospital, his mental status progressively deteriorated. Given the deranged hepatic and renal function, chemotherapy could not be initiated. The patient's family decided against hemodialysis considering his poor prognosis and the patient expired on day 15 of admission. The case report highlights the aggressiveness of one of the rare esophageal malignancies. It is crucial to establish diagnosis at the earlier stages of the disease with prompt treatment in order to avoid serious complications such as hepatorenal syndrome, which resulted in rapid deterioration of our patient's clinical status. More research is necessary in order to establish guidelines to treat neuroendocrine tumors of the esophagus. |
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AbstractList | Neuroendocrine tumors are tumors that arise from the enterochromaffin cells in the neuroendocrine tissue found throughout the body, particularly the digestive tract, pancreas, and thymus. Neuroendocrine tumors of the esophagus are extremely rare and highly aggressive in nature. We present the case of a 55-year-old Hispanic male who initially presented to the emergency department with right-sided abdominal pain. Imaging revealed innumerable lesions occupying half of the liver parenchyma. Subsequent endoscopy with biopsy of the esophageal and liver lesions along with immunohistochemistry staining was suggestive of a large cell neuroendocrine tumor. He later presented with generalized weakness and right-sided abdominal pain with worsening hepatic and renal function. Over the course of the patient's stay in the hospital, his mental status progressively deteriorated. Given the deranged hepatic and renal function, chemotherapy could not be initiated. The patient's family decided against hemodialysis considering his poor prognosis and the patient expired on day 15 of admission. The case report highlights the aggressiveness of one of the rare esophageal malignancies. It is crucial to establish diagnosis at the earlier stages of the disease with prompt treatment in order to avoid serious complications such as hepatorenal syndrome, which resulted in rapid deterioration of our patient's clinical status. More research is necessary in order to establish guidelines to treat neuroendocrine tumors of the esophagus.Neuroendocrine tumors are tumors that arise from the enterochromaffin cells in the neuroendocrine tissue found throughout the body, particularly the digestive tract, pancreas, and thymus. Neuroendocrine tumors of the esophagus are extremely rare and highly aggressive in nature. We present the case of a 55-year-old Hispanic male who initially presented to the emergency department with right-sided abdominal pain. Imaging revealed innumerable lesions occupying half of the liver parenchyma. Subsequent endoscopy with biopsy of the esophageal and liver lesions along with immunohistochemistry staining was suggestive of a large cell neuroendocrine tumor. He later presented with generalized weakness and right-sided abdominal pain with worsening hepatic and renal function. Over the course of the patient's stay in the hospital, his mental status progressively deteriorated. Given the deranged hepatic and renal function, chemotherapy could not be initiated. The patient's family decided against hemodialysis considering his poor prognosis and the patient expired on day 15 of admission. The case report highlights the aggressiveness of one of the rare esophageal malignancies. It is crucial to establish diagnosis at the earlier stages of the disease with prompt treatment in order to avoid serious complications such as hepatorenal syndrome, which resulted in rapid deterioration of our patient's clinical status. More research is necessary in order to establish guidelines to treat neuroendocrine tumors of the esophagus. Neuroendocrine tumors are tumors that arise from the enterochromaffin cells in the neuroendocrine tissue found throughout the body, particularly the digestive tract, pancreas, and thymus. Neuroendocrine tumors of the esophagus are extremely rare and highly aggressive in nature. We present the case of a 55-year-old Hispanic male who initially presented to the emergency department with right-sided abdominal pain. Imaging revealed innumerable lesions occupying half of the liver parenchyma. Subsequent endoscopy with biopsy of the esophageal and liver lesions along with immunohistochemistry staining was suggestive of a large cell neuroendocrine tumor. He later presented with generalized weakness and right-sided abdominal pain with worsening hepatic and renal function. Over the course of the patient's stay in the hospital, his mental status progressively deteriorated. Given the deranged hepatic and renal function, chemotherapy could not be initiated. The patient's family decided against hemodialysis considering his poor prognosis and the patient expired on day 15 of admission. The case report highlights the aggressiveness of one of the rare esophageal malignancies. It is crucial to establish diagnosis at the earlier stages of the disease with prompt treatment in order to avoid serious complications such as hepatorenal syndrome, which resulted in rapid deterioration of our patient's clinical status. More research is necessary in order to establish guidelines to treat neuroendocrine tumors of the esophagus. |
Author | Ilyas, Usman Umar, Zaryab Landry, Ian Otusile, Ibironke |
AuthorAffiliation | 1 Internal Medicine, Icahn School of Medicine at Mount Sinai, Queens Hospital Center, New York City, USA 2 Medicine, Icahn School of Medicine at Mount Sinai, New York City Health and Hospitals/Queens, New York City, USA |
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Cites_doi | 10.1097/PAS.0b013e31826d2639 10.1016/S0344-0338(88)80042-6 10.1016/j.critrevonc.2019.02.012 10.1097/PAS.0b013e31816bf41f 10.7150/jca.29483 10.1530/ERC-17-0012 10.3390/diagnostics5020119 10.1111/pin.12807 10.1371/journal.pone.0173501 10.1634/theoncologist.2018-0382 10.1590/S0004-2803.2017v54n1-01 10.5858/2000-124-0411-ECTLCN 10.1159/000441381 10.1007/s12328-019-00995-7 10.32074/1591-951X-229 10.14309/01.ajg.0000709760.01277.b6 |
ContentType | Journal Article |
Copyright | Copyright © 2022, Umar et al. Copyright © 2022, Umar et al. This work is published under https://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Copyright © 2022, Umar et al. 2022 Umar et al. |
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Keywords | esophageal cancer neuroendocrine carcinoma of esophagus large cell neuroendocrine carcinoma hepatorenal syndrome neuroendocrine neoplasm |
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References_xml | – volume: 37 year: 2013 ident: ref10 article-title: Primary high-grade neuroendocrine carcinoma of the esophagus: a clinicopathologic and immunohistochemical study of 42 resection cases publication-title: Am J Surg Pathol doi: 10.1097/PAS.0b013e31826d2639 – volume: 183 year: 1988 ident: ref13 article-title: Neuroendocrine tumors of the gastrointestinal tract publication-title: Pathol Res Pract doi: 10.1016/S0344-0338(88)80042-6 – volume: 137 year: 2019 ident: ref6 article-title: A rare rarity: Neuroendocrine tumor of the esophagus publication-title: Crit Rev Oncol Hematol doi: 10.1016/j.critrevonc.2019.02.012 – volume: 32 year: 2008 ident: ref9 article-title: Retrospective study of clinicopathologic features and prognosis of high-grade neuroendocrine carcinoma of the esophagus publication-title: Am J Surg Pathol doi: 10.1097/PAS.0b013e31816bf41f – volume: 10 year: 2019 ident: ref15 article-title: A 10-year population-based study of the differences between NECs and carcinomas of the esophagus in terms of clinicopathology and survival publication-title: J Cancer doi: 10.7150/jca.29483 – volume: 24 year: 2017 ident: ref11 article-title: Genetic and epigenetic drivers of neuroendocrine tumours (NET) publication-title: Endocr Relat Cancer doi: 10.1530/ERC-17-0012 – volume: 5 year: 2015 ident: ref7 article-title: Neuroendocrine carcinomas of the gastroenteropancreatic system: a comprehensive review publication-title: Diagnostics (Basel) doi: 10.3390/diagnostics5020119 – volume: 69 year: 2019 ident: ref5 article-title: A case of large cell neuroendocrine carcinoma exhibiting rhabdoid features in the esophagogastric junction publication-title: Pathol Int doi: 10.1111/pin.12807 – volume: 12 year: 2017 ident: ref3 article-title: Neuroendocrine carcinoma of the esophagus: clinicopathological and immunohistochemical features of 14 cases publication-title: PLoS One doi: 10.1371/journal.pone.0173501 – volume: 24 year: 2019 ident: ref17 article-title: High-grade gastrointestinal neuroendocrine carcinoma management and outcomes: a National Cancer Database study publication-title: Oncologist doi: 10.1634/theoncologist.2018-0382 – volume: 54 year: 2017 ident: ref4 article-title: Primary neuroendocrine neoplasm of the esophagus - Report of 14 cases from a single institute and review of the literature publication-title: Arq Gastroenterol doi: 10.1590/S0004-2803.2017v54n1-01 – volume: 124 year: 2000 ident: ref14 article-title: Esophageal collision tumor (large cell neuroendocrine carcinoma and papillary carcinoma) arising in a Barrett esophagus publication-title: Arch Pathol Lab Med doi: 10.5858/2000-124-0411-ECTLCN – volume: 9 year: 2015 ident: ref8 article-title: Large-cell neuroendocrine carcinoma of the esophagus: a case from Saudi Arabia publication-title: Case Rep Gastroenterol doi: 10.1159/000441381 – volume: 12 year: 2019 ident: ref16 article-title: Neuroendocrine carcinoma of the esophagus with an adenocarcinoma component publication-title: Clin J Gastroenterol doi: 10.1007/s12328-019-00995-7 – volume: 113 year: 2021 ident: ref2 article-title: Neuroendocrine neoplasms of the esophagus and stomach publication-title: Pathologica doi: 10.32074/1591-951X-229 – volume: 115 year: 2020 ident: ref1 article-title: A case of esophageal neuroendocrine tumor presenting as abdominal pain publication-title: Am J Gastroenterol doi: 10.14309/01.ajg.0000709760.01277.b6 – volume: 66 year: 2011 ident: ref12 article-title: Neuroendocrine tumors involving the gastroenteropancreatic tract: a clinicopathological evaluation of 773 cases publication-title: Clinics (Sao Paulo) |
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SubjectTerms | Abdomen Acidosis Antigens Biopsy Cancer Case reports Chemotherapy Creatinine Cytokeratin Esophageal cancer Esophagus Gastroenterology Laboratories Liver Medical imaging Metabolism Metastasis Morphology Nephrology Neuroendocrine tumors Oncology Phosphatase Stem cells |
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