Cargando…

Hepatic Cyst: An Unusual Suspect of Syncope

The patient is a 75-year-old man with history of diabetes and hypertension who presented with syncope after experiencing sharp, 10/10 right flank and abdominal pain worsening over three weeks associated with decreased appetite. Physical examination revealed hepatomegaly and right lower quadrant (RUQ...

Descripción completa

Detalles Bibliográficos
Autores principales: Choudhry, Mohammad K., Xiong, Bei, Anandaraj, Antony, Trillo, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064878/
https://www.ncbi.nlm.nih.gov/pubmed/32181027
http://dx.doi.org/10.1155/2020/1659718
_version_ 1783504951033462784
author Choudhry, Mohammad K.
Xiong, Bei
Anandaraj, Antony
Trillo, John
author_facet Choudhry, Mohammad K.
Xiong, Bei
Anandaraj, Antony
Trillo, John
author_sort Choudhry, Mohammad K.
collection PubMed
description The patient is a 75-year-old man with history of diabetes and hypertension who presented with syncope after experiencing sharp, 10/10 right flank and abdominal pain worsening over three weeks associated with decreased appetite. Physical examination revealed hepatomegaly and right lower quadrant (RUQ) tenderness, negative for peritoneal signs. Bloodwork showed leukocytosis (13 K/mcl), alkaline phosphatase (141 U/L), total bilirubin (2.0 mg/dL), and gamma-glutamyl transferase (172 U/L). Computed Tomography (CT) revealed multiple hepatic cysts with the largest measuring 17 × 14 × 18 cm (Figure 1). Parenteral opiates provided minimal relief. Cardiac and neurologic etiologies of syncope were ruled out. The patient's course was complicated by opioid-induced delirium as his abdominal pain progressively worsened despite escalating doses of parenteral and oral analgesics. Gastroenterology and interventional radiology consulted to evaluate for Glisson's capsular stretch. Therapeutic aspiration yielded 2.5 L of serous fluid, which alleviated the patient's pain. Cytology was negative for malignancy. Opiates were titrated down. Repeat CT (Figure 2) showed cysts that were significantly reduced in size. The patient showed complete resolution of symptoms and was subsequently discharged. We present a rare case of a large hepatic cyst causing syncope. In the appropriate clinical setting, syncope with RUQ tenderness and hepatomegaly should raise the index of suspicion for hepatic cysts.
format Online
Article
Text
id pubmed-7064878
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-70648782020-03-16 Hepatic Cyst: An Unusual Suspect of Syncope Choudhry, Mohammad K. Xiong, Bei Anandaraj, Antony Trillo, John Case Reports Hepatol Case Report The patient is a 75-year-old man with history of diabetes and hypertension who presented with syncope after experiencing sharp, 10/10 right flank and abdominal pain worsening over three weeks associated with decreased appetite. Physical examination revealed hepatomegaly and right lower quadrant (RUQ) tenderness, negative for peritoneal signs. Bloodwork showed leukocytosis (13 K/mcl), alkaline phosphatase (141 U/L), total bilirubin (2.0 mg/dL), and gamma-glutamyl transferase (172 U/L). Computed Tomography (CT) revealed multiple hepatic cysts with the largest measuring 17 × 14 × 18 cm (Figure 1). Parenteral opiates provided minimal relief. Cardiac and neurologic etiologies of syncope were ruled out. The patient's course was complicated by opioid-induced delirium as his abdominal pain progressively worsened despite escalating doses of parenteral and oral analgesics. Gastroenterology and interventional radiology consulted to evaluate for Glisson's capsular stretch. Therapeutic aspiration yielded 2.5 L of serous fluid, which alleviated the patient's pain. Cytology was negative for malignancy. Opiates were titrated down. Repeat CT (Figure 2) showed cysts that were significantly reduced in size. The patient showed complete resolution of symptoms and was subsequently discharged. We present a rare case of a large hepatic cyst causing syncope. In the appropriate clinical setting, syncope with RUQ tenderness and hepatomegaly should raise the index of suspicion for hepatic cysts. Hindawi 2020-02-28 /pmc/articles/PMC7064878/ /pubmed/32181027 http://dx.doi.org/10.1155/2020/1659718 Text en Copyright © 2020 Mohammad K. Choudhry et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Choudhry, Mohammad K.
Xiong, Bei
Anandaraj, Antony
Trillo, John
Hepatic Cyst: An Unusual Suspect of Syncope
title Hepatic Cyst: An Unusual Suspect of Syncope
title_full Hepatic Cyst: An Unusual Suspect of Syncope
title_fullStr Hepatic Cyst: An Unusual Suspect of Syncope
title_full_unstemmed Hepatic Cyst: An Unusual Suspect of Syncope
title_short Hepatic Cyst: An Unusual Suspect of Syncope
title_sort hepatic cyst: an unusual suspect of syncope
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064878/
https://www.ncbi.nlm.nih.gov/pubmed/32181027
http://dx.doi.org/10.1155/2020/1659718
work_keys_str_mv AT choudhrymohammadk hepaticcystanunusualsuspectofsyncope
AT xiongbei hepaticcystanunusualsuspectofsyncope
AT anandarajantony hepaticcystanunusualsuspectofsyncope
AT trillojohn hepaticcystanunusualsuspectofsyncope