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  4. An Unusual Cause of Severe Granulomatous Hepatitis and Jaundice.
 
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Titre

An Unusual Cause of Severe Granulomatous Hepatitis and Jaundice.

Type
étude de cas
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
The American Journal of Gastroenterology  
Auteur(s)
Coukos, A.
Auteure/Auteur
Uldry, E.
Auteure/Auteur
Meylan, S.
Auteure/Auteur
Schmidt, S.
Auteure/Auteur
Fasquelle, F.
Auteure/Auteur
Sempoux, C.
Auteure/Auteur
Fraga, M.
Auteure/Auteur
Liens vers les personnes
Schmidt Kobbe, Sabine  
Sempoux, Christine  
Coukos, Alexander  
Fraga Christinet, Montserrat  
Uldry, Emilie  
Meylan, Sylvain  
Fasquelle, Francois  
Liens vers les unités
Radiodiagnostic & radiol. Interven.  
Institut universitaire de pathologie (IUPA)  
Gastro-entérologie  
Chirurgie viscérale  
Maladies infectieuses  
ISSN
1572-0241
Statut éditorial
Publié
Date de publication
2023-11-01
Volume
118
Numéro
11
Première page
1920
Peer-reviewed
Oui
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
A 22-year-old Syrian man with a history of radiologically and serologically documented cystic echinococcosis presented intense acute abdominal pain and sepsis 2 months after a journey in Iraq. Liver biochemistries were minimally elevated (alanine transaminase 88 IU/L, alkaline phosphatase 150 IU/L) with marked hyperbilirubinemia (total bilirubin 5.7 mg/dL, direct bilirubin 4.7 mg/dL), elevated C-reactive protein (306 mg/L), and anemia (hemoglobin 8.9 g/dL). Abdominal computed tomography and magnetic resonance imaging showed fistulation of the known hydatid cyst to the intrahepatic biliary tree and an adjacent arterial pseudoaneurysm (arrow) (a). Endoscopic retrograde cholangiopancreatography enabled drainage of the fistulated cyst (b). The arterial pseudoaneurysm was embolized. Despite drainage and broad-spectrum antibiotics, liver function tests and jaundice worsened. A liver biopsy showed acute severe hepatitis with necrotic foci, numerous portal and lobular granulomas forming nodules, with some giant cells, and dystrophic bile ducts (c). The cultured bile revealed Salmonella enterica serotype paratyphi B. The presentation was consistent with typhoid fever due to Salmonella typhi-infected liver cyst. The patient recovered after a 2-month piperacillin-tazobactam antibiotic regimen. Typhoid fever is associated with a mortality of approximately 15% in the preantibiotic era which is <1% with appropriate treatment. Hepatitis arises in around 5% of cases. Pathogens include S. enterica serotypes typhi, paratyphi A, and rarely, Salmonella paratyphi B and C. Histopathologically, hepatocellular necrosis together with granulomatous agglomerates of Kupffer cells are characteristic lesions. Salmonella is the second most common cause of potentially lethal infectious arterial pseudoaneurysms, requiring swift intravascular treatment. Although rare in Western regions, typhoid fever must be considered in any case of abdominal pain with sepsis on return from an endemic region. (Informed consent was obtained from the patient to publish these images.)
Sujets

Humans

Jaundice/etiology

Hepatitis/complicatio...

Hepatitis/diagnosis

Granuloma/diagnosis

Granuloma/etiology

Jaundice, Obstructive...

PID Serval
serval:BIB_E1B8A245AB14
DOI
10.14309/ajg.0000000000002358
PMID
37307563
WOS
001102204200006
Permalien
https://iris.unil.ch/handle/iris/260154
Date de création
2023-06-15T16:00:43.420Z
Date de création dans IRIS
2025-05-21T07:22:55Z
Fichier(s)
En cours de chargement...
Vignette d'image
Nom

Coukos Case report Am J Gastroenterol 2023.pdf

Version du manuscrit

published

Licence

https://iris.unil.ch/disclaimer

Taille

213.78 KB

Format

Adobe PDF

PID Serval

serval:BIB_E1B8A245AB14.P001

Somme de contrôle

(MD5):b95002a4d5b5706db25e774ce1bfdbaa

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