Case Reports in Hepatology
Volume 2019 (2019), Article ID 8459205, 3 pages
https://doi.org/10.1155/2019/8459205

Case Report

Acute Hepatitis Secondary to the Use of Ilex paraguariensis (Mate Tea): A Case Report and Review of Literature

Eduardo A. Rodriguez, Raquel Teixeira Yokoda, David E. Payton, Rish Pai, and Thomas J. Byrne

Mayo Clinic Arizona, 5777 E Mayo Blvd, Phoenix, AZ 85054, USA

Correspondence should be addressed to Eduardo A. Rodriguez; erodrigu18@yahoo.com

Received 1 July 2019; Accepted 9 August 2019; Published 13 October 2019

Academic Editor: Mauro Vigano

Copyright © 2019 Eduardo A. Rodriguez et al. 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.

Abstract.

Drug induced liver injury is a very frequent cause of hepatotoxicity and within that group, herbal and dietary supplements are a well described subcategory. The following clinical vignette describes the case of a young man with acute hepatitis secondary to the use of Ilex paraguariensis, also known as yerba mate, which is a herbal product commonly drunk in South America. This is the first written case of mate tea induced hepatotoxicity.

1. Introduction

Drug induced liver injury (DILI) can occur following the use of both prescription and/or over the counter medications. Even though it is not as frequent as other more common causes of liver injury such as viral hepatitis, it remains to be an important differential diagnosis category that the smart clinician should always consider. Within this category herbal and dietary supplements (HDS) are a frequent cause of hepatotoxicity [1]. The following clinical vignette describes the case of acute hepatitis secondary to the use of Ilex paraguariensis, also known as yerba mate.

2. Case Presentation

A 21-year-old American gentleman without significant past medical history was transferred from northern Argentina for further investigation of elevated liver enzymes. He had spent the last four months over there as part of his church mission and during the latter two weeks of vacation had initially noted mildly icteric sclera, followed by generalized malaise, jaundice, pruritus, and dark urine. He denied fever, chills, diaphoresis, alcohol intake, over the counter medications, illicit drug use including IV drugs, and recent sexual encounters. He also denied other abdominal complaints such as pain, bloating, nausea, vomiting, and diarrhea. Initial workup abroad included negative viral hepatitis serologies, negative autoimmune markers as well as negative magnetic resonance cholangiopancreatography. Due to the lack of improvement, the family of the patient decided to return him to the U.S. for further evaluation.

On presentation his vital signs were stable. His physical exam was normal except for jaundice. He did not have any neurological deficit. The laboratory findings were as follows: total bilirubin, 32.9 mg/dL: direct bilirubin > 18.0 mg/dL, alanine aminotransferase (ALT), 2685 U/L; aspartate aminotransferase (AST), 1842 U/L, alkaline phosphatase (ALP) 129 U/L. RUCAM score was 65.4. He had negative viral hepatitis markers including hepatitis A, B, C, E, cytomegalovirus, herpes simplex, adenovirus, and varicella zoster virus.

Autoimmune panel including anti smooth muscle antibody (ASMA), anti nuclear antibody (ANA), anti mitochondrial antibody (AMA) and LKM1 antibody were all negative/unremarkable. Further serologies for Entamoeba histolitica and Schistosoma mansoni were also obtained given the geographical location of his mission, and these were negative. Urine toxicology screen was negative for alcohol, amphetamines, barbiturates, benzodiazepenes, cocaine, opiates, and tetrahydrocannabinol. Acetaminophen level in blood was undetectable (Table 1).

Table 1: Laboratory data on admission.

Complete blood count

White blood cell count
5900
/µL

Hemoglobin
14.2
g/dL

Platelets
350
10³/µL

Coagulation

PT
13.6
sec

INR
1.2

Complete metabolic panel

Albumin
4.7
g/dL

Total bilirubin
32.9
mg/dL

Direct bilirubin
>18
mg/dL

AST
1842
U/L

ALT
2685
U/L

ALP
129
U/L

Lipase
20
U/L

BUN
7.5
mg/dL

Creatinine
0.69
mg/dL

eGFR
>90
mL/min

Immunology

ANA
0.4
Dil

AMA
<0.1
Index

anti-LKM1 Ab
<5.0
Index

ASMA
Negative
Index

Alpha-antitrypsin
177
mg/dL

Infectious markers

HCVAb
Negative

HCV-RNA
Undetectable

HBsAg
Negative

HBcgM Ab
Negative

HAV-IgM
Negative

HEV-IgM
Negative

HTLV-1 Ab
Negative

EBV-IgG
Negative

EBV-IgM
Negative

CMV-IgG
Negative

CMV-IgM
Negative

VZV-IgG
Negative

VZV-IgM
Negative

HSV-IgG
Negative

HSV-IgM
Negative

Adenovirus PCR
Negative

Toxicology and drug testing

Acetominophen, S
<5.0
mcg/mL

Ethanol, U
Undetectable

Amphetamines, U
Undetectable

Barbiturates, U
Undetectable

Benzodiazepines, U
Undetectable

Cocaine, U
Undetectable

Methadone metabolite, U
Undetectable

Opiates, U
Undetectable

Tetrahydrocannabinnol, U
Undetectable

Upon further questioning he reported daily yerba mate tea during the four months he spent in Argentina, sometimes twice a day and symptoms began during the last two weeks he stayed there. He continued drinking the tea until the last day of his vacations, before coming back to the United States. He also added the fact that all of his co-workers had drunk the same tea on a daily basis however no one else developed similar complaints.

In order to further investigate the etiology of his acute hepatitis an ultrasound-guided liver biopsy was obtained. Histological evaluation revealed an acute cholestatic hepatitis pattern, without typical features for autoimmune hepatitis. It demonstrated expanded portal tracts with a mixed inflammatory cell infiltrate composed of lymphocytes as well as occasional eosinophils and neutrophils. A mild bile ductular reaction was also present at the periphery of these portal areas, likely in response to the hepatocellular injury and likely explaining the elevated RUCAM score. Significant lobular disarray with numerous foci of lobular inflammation and acidophil bodies was appreciated. Iron stain demonstrated scattered Kupffer cell iron. PAS with diastase stain was negative for intracytoplasmic globules. Plasma cells were not prominent. The trichrome and reticulin stains confirmed the absence of fibrosis. Overall, the morphologic changes noted were thought to be found most commonly in the setting of medication or toxin-induced injury (including herbal medication) (Figure 1).

(a)

(b)

Figure 1: Acute cholestatic hepatitis. (a) Portal inflammation with bile ductular reaction and periportal hepatocyte injury (H&E 100X). (b) Lobular disarray characterized by lobular inflammation, acidophil bodies, and cholestasis (H&E 200X).

Even though liver markers initially rose, after two days hepatic panel numbers started to downtrend, and the patient was discharged from the hospital. In the outpatient setting patient was monitored closely with liver panel labs. After two months of close follow up, all numbers came back to normal levels, and patient was discharged from clinic (Figure 2). Except for the temporary jaundice and malaise, he remained asymptomatic throughout.

Figure 2: Trend of liver enzymes during admission and in the outpatient setting.

3. Discussion

HDS liver injury shares the same underlying biochemical process with DILI in which the foreign chemical needs to be metabolized in order to be eliminated. It is during that process that potential hepatotoxic metabolites can be produced and cause injury in susceptible patients [2]. Most cases of herbal hepatotoxicity reflect an idiosyncratic pattern, which means reactions can occur unpredictably in the population. The other group includes those products that cause intrinsic injury, which means predictable reactions in humans or in animal models when enough dose of the offending agent is administered. Acetaminophen is the prototypic cause of intrinsic injury [1]. In order to consider DILI, other more common etiologies should be rule ruled out first. In this case, we performed a thorough evaluation including viral hepatitis panel as well as autoimmune markers due to the significantly elevated transaminases initially noted, and given the young age of the patient.

After an extensive evaluation which included a liver biopsy that ultimately suggested medication/toxin (including possible HDS) effect, we consider that the main cause of the acute hepatitis in this case was Ilex paraguariensis, also known as yerba mate, which the patient drank while in Argentina. The present case describes the first reported case of HDS injury secondary to the use of yerba mate, a common herbal product that is drunk as a tea in the southern portion of South America, namely Argentina, Brazil, Paraguay, and Uruguay [3]. In these countries the leaves and stems of the plant are processed in the production of several types of beverages including mate or chimarrao (warm), as well as various types of teas and carbonated drinks. Some of the attributed biological properties include an antioxidant and hypocholesterolemic capacity as well as possible cancer prevention properties [4]. It is also possible that some of these drinks might have the presence of adulterants that may be incorporated into the final product, either intentionally or unintentionally.

Pathogenesis is difficult to characterize in HDS injury as this is mainly a human and not animal process and thus experimental data on animals are limited. However, some of the available experimental studies have described an intrinsic pattern of HDS with the possible involvement of unsaturated pyrrolizidine alkaloids (PAs). These can damage the endothelial cells of the liver and reduce the sinusoidal blood flow, causing clinical features of hepatic sinusoidal obstruction syndrome [2]. In our case, the hepatotoxic pattern was cholestatic which correlates with a possible hepatic sinusoidal obstruction syndrome-like presentation.

Liver injury from HDS is a growing and challenging problem. Further clinical and basic science research as well as better monitoring and regulatory efforts is needed in order to insure consumer safety [5].

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this article.

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