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...

Full description

Saved in:
Bibliographic Details
Published inCurēus (Palo Alto, CA) Vol. 14; no. 4; p. e23720
Main Authors Umar, Zaryab, Ilyas, Usman, Otusile, Ibironke, Landry, Ian
Format Journal Article
LanguageEnglish
Published United States Springer Nature B.V 01.04.2022
Cureus
Subjects
Online AccessGet full text

Cover

Loading…
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.
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
AuthorAffiliation_xml – name: 2 Medicine, Icahn School of Medicine at Mount Sinai, New York City Health and Hospitals/Queens, New York City, USA
– name: 1 Internal Medicine, Icahn School of Medicine at Mount Sinai, Queens Hospital Center, New York City, USA
Author_xml – sequence: 1
  givenname: Zaryab
  surname: Umar
  fullname: Umar, Zaryab
– sequence: 2
  givenname: Usman
  surname: Ilyas
  fullname: Ilyas, Usman
– sequence: 3
  givenname: Ibironke
  surname: Otusile
  fullname: Otusile, Ibironke
– sequence: 4
  givenname: Ian
  surname: Landry
  fullname: Landry, Ian
BackLink https://www.ncbi.nlm.nih.gov/pubmed/35509743$$D View this record in MEDLINE/PubMed
BookMark eNpdkb1PwzAQxS0EgvKxMaNILAwE7NixnQUJVXyqgoEyW65zaVMldrETpP73uLRUwHQn3U_v7t47RLvWWUDolOArIfLi2vQe-nCVUZHhHTTICJepJJLt_uoP0EkIc4wxwZESeB8d0DzHhWB0gJ5H2k8hHULTJHfBLWZ6CrpJXqD3DmzpjK8tJOO-dT4ZgS5rO006lzzCQnfOg43s29KW3rVwjPYq3QQ42dQj9H5_Nx4-pqPXh6fh7Sg1WVF0KRU5yIIL4Bll0jDAVQGSkRxyDpmRJSNlyQ2IYoIrzRjOq0pMOKYZp6AlpkfoZq276CctlAZs53WjFr5utV8qp2v1d2LrmZq6T1VgjqNpUeBiI-DdRw-hU20dTHRAW3B9UBnn0SvC-GrX-T907nofv15RgkiRU8Ijdfb7ou0pPzZH4HINGO9C8FBtEYLVKki1DlJ9B0m_AIXrkQM
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.
Copyright_xml – notice: Copyright © 2022, Umar et al.
– notice: 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.
– notice: Copyright © 2022, Umar et al. 2022 Umar et al.
DBID AAYXX
CITATION
NPM
3V.
7X7
7XB
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
K9.
M0S
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOI 10.7759/cureus.23720
DatabaseName CrossRef
PubMed
ProQuest Central (Corporate)
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Health & Medical Complete (Alumni)
ProQuest Health & Medical Collection
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest One Academic Eastern Edition
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Central China
ProQuest Hospital Collection (Alumni)
ProQuest Central
ProQuest Health & Medical Complete
Health Research Premium Collection
ProQuest One Academic UKI Edition
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
ProQuest Central (New)
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

PubMed
Publicly Available Content Database
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X7
  name: Health & Medical Collection
  url: https://search.proquest.com/healthcomplete
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2168-8184
ExternalDocumentID PMC9060759
35509743
10_7759_cureus_23720
Genre Case Reports
GroupedDBID 53G
5VS
7X7
8FI
8FJ
AAYXX
ABUWG
ADBBV
AFKRA
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BCNDV
BENPR
BPHCQ
BVXVI
CCPQU
CITATION
FYUFA
HMCUK
HYE
KQ8
M48
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
RPM
UKHRP
3V.
ADRAZ
GROUPED_DOAJ
NPM
OK1
7XB
8FK
AZQEC
DWQXO
K9.
PKEHL
PQEST
PQUKI
PRINS
7X8
5PM
ID FETCH-LOGICAL-c299t-375e8967e62348c4e0f9e8415e56e2c8d41dd6ce79b0fa4405ff7b603263ea803
IEDL.DBID M48
ISSN 2168-8184
IngestDate Thu Aug 21 13:46:22 EDT 2025
Fri Jul 11 09:35:27 EDT 2025
Mon Jun 30 07:29:29 EDT 2025
Thu Jan 02 22:54:20 EST 2025
Tue Jul 01 03:27:46 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords esophageal cancer
neuroendocrine carcinoma of esophagus
large cell neuroendocrine carcinoma
hepatorenal syndrome
neuroendocrine neoplasm
Language English
License Copyright © 2022, Umar et al.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c299t-375e8967e62348c4e0f9e8415e56e2c8d41dd6ce79b0fa4405ff7b603263ea803
Notes ObjectType-Case Study-2
SourceType-Scholarly Journals-1
content type line 14
ObjectType-Feature-4
ObjectType-Report-1
ObjectType-Article-3
content type line 23
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.7759/cureus.23720
PMID 35509743
PQID 2671875316
PQPubID 2045583
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_9060759
proquest_miscellaneous_2660101460
proquest_journals_2671875316
pubmed_primary_35509743
crossref_primary_10_7759_cureus_23720
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-04-01
PublicationDateYYYYMMDD 2022-04-01
PublicationDate_xml – month: 04
  year: 2022
  text: 2022-04-01
  day: 01
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Palo Alto
– name: Palo Alto (CA)
PublicationTitle Curēus (Palo Alto, CA)
PublicationTitleAlternate Cureus
PublicationYear 2022
Publisher Springer Nature B.V
Cureus
Publisher_xml – name: Springer Nature B.V
– name: Cureus
References Tustumi F (ref4) 2017; 54
Kuriry H (ref8) 2015; 9
Estrozi B (ref12) 2011; 66
Maru DM (ref9) 2008; 32
Huang Q (ref10) 2013; 37
Everwine M (ref1) 2020; 115
Di Domenico A (ref11) 2017; 24
Giannetta E (ref6) 2019; 137
Ilett EE (ref7) 2015; 5
Alese OB (ref17) 2019; 24
Ichimata S (ref5) 2019; 69
Egashira A (ref3) 2017; 12
Kaneko Y (ref16) 2019; 12
Chejfec G (ref13) 1988; 183
Cai W (ref15) 2019; 10
Mastracci L (ref2) 2021; 113
Wilson CI (ref14) 2000; 124
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)
SSID ssj0001072070
Score 2.1784387
Snippet Neuroendocrine tumors are tumors that arise from the enterochromaffin cells in the neuroendocrine tissue found throughout the body, particularly the digestive...
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
StartPage e23720
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
SummonAdditionalLinks – databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3fS8MwEA46QXwRf1udUkEf67KuTdInkbExxuaLG-ytpM0VhdnOrf3_vWu76RR8Tpq2l8vdd8nlO8bujdFtzXniaL8dOR4CZEcrwx0d8cgXcaITQ7eRxy9iMPWGM39Wb7it6rTKtU0sDbXJYtojb7kCrShi67Z4Wnw6VDWKTlfrEhq7bI-oy0ir5Ux-77Fw6aJKV_nuUvpBKy6WUKweXarNsu2J_sDL31mSP9xO_4gd1njRfq4m-JjtQHrC9sf1ifgpG44oldvpwnxu96gkAdoH7F9ybkCKv0W3--xJ8ZEt7VGVMG_nmT1AL4TRNtDYrzVpwRmb9nuT7sCp6yM4MTqRHG2DDyoQEhDCeCr2gCcBKPTI4AtwY2W8tjEiBhlEPNEeQrMkkZHgiNg6oBXvnLNGmqVwyWwljAfEVONqDJhNEIFyPeMbpTDAAgEWe1jLKlxUNBghhg8k07CSaVjK1GLNtSDDejFgy2bqLHa3aUY1prMJnUJGTwtRlg0WOMRFJffNixAScQx7OhaTWzOy6UAU2dst6ftbSZUdcIGYKLj6_7Ou2YFLtxrKhJwma-TLAm4Qa-TRbalQX731108
  priority: 102
  providerName: ProQuest
Title Large-Cell Esophageal Neuroendocrine Tumor Leading to Hepatorenal Syndrome
URI https://www.ncbi.nlm.nih.gov/pubmed/35509743
https://www.proquest.com/docview/2671875316
https://www.proquest.com/docview/2660101460
https://pubmed.ncbi.nlm.nih.gov/PMC9060759
Volume 14
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwdV1ZS8QwEB48QHwRb9djqaCPXdNumqRPorKyiCuiLuxbSZspCmure4D-eyc9FtfjOekUJtN83zST-QBOjNGeZix1deDFLieC7GplmKtjFgciSXVq7G3k3p3o9vnNIBgsQK02Wjlw_GdqZ_Wk-qNh6-P985w-eOKvLSmD8CyZjnA6bvlWcGURlgmTpNUy6FVEv_jbwmisUI7zPaFcQileVsH_MrAKKwTBjGh2ex6qfvHPn2WU33Dpeh3WKkLpXJQRsAELmG3CSq86Mt-Cm1tb6-1e4XDodKxmAW0gNL9oyoGZyRN7_c95mr7mI-e2rKh3JrnTJZiidByt7ceqq8E29K87T1ddtxJQcBNCmQltHgGqUEgkjsNVwpGlISqCbAwE-oky3DNGJCjDmKWaE3dLUxkLRpSujVqx9g4sZXmGe-AoYTjaVja-pozahDEqn5vAKEUZGApswGntq-it7JMRUX5h3RuV7o0K9zbgsHZkVC925AtCSMqbPNGA49kwxbk9vNAZ5vZpIQpdYUEmdku_z15UL1gD5NyKzCbYHtrzI9nLc9FLO2SCSFO4_6_NA1j17Y2HoljnEJYmoykeEQ-ZxE1YlAPZhOXLzt39Q7MIuC_yE96u
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LT9wwEB5RkFouCFoKSykNUjmmeL2J7RwqhChogV0uXaS9BSeeqJUggWVXiD_Fb2Qmj4UFiRtnO070eTzzTTwPgJ_O2bYVIvNt2E78gAiyb40Tvk1EEqo0s5njbOT-meqeByfDcDgHD00uDIdVNjqxVNSuSPkf-a5UpEWJW7fV3vWNz12j-Ha1aaFRicUp3t-Ry3b7-_gP7e-OlEeHg4OuX3cV8FNSvWM6USGaSGkkwx-YNECRRWjIjmGoUKbGBW3nVIo6SkRmAyI0WaYTJYjndNAa0aF1P8ACGV7Bzp4e6qd_OkJLOkJVfL3WYbSbTkY4uf0luRfMrOV7RWdfRmU-M3NHy7BU81NvvxKoFZjD_DN87Nc38F_gpMeh4_4BXl56h9wCgfQRzS9rfGBOMHI2oTeYXBUjr1cF6HvjwuuS1SPvHnntv3WRhFU4fxfkvsJ8XuS4Dp5RLkCujCMtOeguStDIwIXOGHLoUGELdhqs4uuq7EZM7gpjGleYxiWmLdhsgIzrw0cjU1FpwfZ0mI4N34XYHAt-WqmyTbGiJdYq3KcvIgomyM3qtEDP7Mh0Apfknh3J__8rS3NHQhEHizbe_qwf8Kk76Pfi3vHZ6TdYlJxRUQYDbcL8eDTB78RzxslWKVweXLy3ND8CVO4Tfw
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LT9tAEB5BkBCXipZXeLRGgqPJZmOv1wdUUUgUIESIh8TNrL1jtRK1ISSq-tf4dZ3xI22oxI3zrtfWtzOz33jnAbBnrWkbIVLX-O3Y9Yggu0Zb4ZpYxL5KUpNazka-GKr-rXd259_NwUudC8NhlbVNLAy1zRP-R96Siqwoceu2aqVVWMTlSe_r45PLHaT4prVup1GKyDn-_kXu2_Ph6Qnt9b6Uve7Ncd-tOgy4CZnhMWmXjzpUARIJ8HTioUhD1HSmoa9QJtp6bWtVgkEYi9R4RG7SNIiVIM7TQaNFh9adh4WAvaIGLHzrDi-v_v7hEYEkhSqj7YPAD1vJZIST5wPJnWFmz8H_yO3rGM1_Dr3eMnyo2KpzVIrXR5jD7BMsXlT38StwNuBAcvcYHx6cLjdEIOtE84uKH5gRqJxb6NxMfuYjZ1CG6zvj3OnTGUi-PvLa11XJhFW4fRfs1qCR5RlugKOV9ZDr5EhD7roNY9TSs77Vmtw7VNiE_Rqr6LEswhGR88KYRiWmUYFpE7ZrIKNKFWlkKjhN2J0OkxLxzYjJMOenlSqaFitaYr3EffoiImSCnK5OE4KZHZlO4ALdsyPZj-9Foe5QKGJk4ebbn_UFFkmSo8Hp8HwLliSnVxSRQdvQGI8muEOkZxx_rqTLgfv3Fug_kFYZGg
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Large-Cell+Esophageal+Neuroendocrine+Tumor+Leading+to+Hepatorenal+Syndrome&rft.jtitle=Cur%C4%93us+%28Palo+Alto%2C+CA%29&rft.au=Umar%2C+Zaryab&rft.au=Ilyas%2C+Usman&rft.au=Otusile%2C+Ibironke&rft.au=Landry%2C+Ian&rft.date=2022-04-01&rft.issn=2168-8184&rft.eissn=2168-8184&rft.volume=14&rft.issue=4&rft.spage=e23720&rft_id=info:doi/10.7759%2Fcureus.23720&rft_id=info%3Apmid%2F35509743&rft.externalDocID=35509743
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2168-8184&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2168-8184&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2168-8184&client=summon