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Heap of stones: An unusual cause for biliary colic and elevated liver function tests
Henning Wittenburg
Corresponding author
henning.wittenburg@medizin.uni-leipzig.de

Correspondence and reprint request:
, Volker Keim, Albrecht Hoffmeister
University Hospital of Leipzig, Department of Internal Medicine, Neurology and Dermatology, Division of Gastroenterology and Rheumatology, Liebigstrasse 20, 04103 Leipzig, Germany
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="s0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="st0015">Case Report</span><p id="p0005" class="elsevierStylePara elsevierViewall">A 40-year old woman presented to our emergency department due to recurrent abdominal pain in the right upper quadrant with no fever or jaundice consistent with biliary colics&#46; A cholecystectomy for symptomatic cholecystolithiasis was performed four years previously&#46; Besides hypothyroidism&#44; the past medical history was unremarkable&#46; Physical exam revealed adiposity grade 1 &#40;BMI 32&#41; and tenderness in the right upper quadrant&#46; Liver function tests &#40;ASAT&#44; ALAT&#44; GGT&#44; AP&#44; total bilirubin&#41; were slightly elevated&#46; Abdominal ultrasound showed multiple small hyperechoic foci with complete acoustic shadows in the ventral segments of the right liver lobe &#40;<a class="elsevierStyleCrossRef" href="#f0005">Figure 1A</a>&#44; arrows&#41;&#46; These finding were confirmed on MRCP &#40;not shown&#41;&#46; For removal of symptomatic intrahepatic gallstones&#44; an ERCP was performed &#40;<a class="elsevierStyleCrossRef" href="#f0005">Figure 1B</a>&#41;&#46; The cholangiogram showed trifurcation of the hilus and confirmed dilatation of the bile ducts filled with multiple intraductalar small calculi in liver segment V only &#40;<a class="elsevierStyleCrossRef" href="#f0005">Figure 1B</a>&#44; arrowheads&#41;&#46; Employing dormia baskets and stone extraction balloons&#44; gallstones were removed from the intrahepatic bile ducts&#46; Gross appearance of multiple small&#44; round&#44; white to yellowish calculi suggested cholesterol gallstones &#40;<a class="elsevierStyleCrossRef" href="#f0005">Figure 1C</a>&#41;&#46; Finally&#44; following repeated ERCPs&#44; the intrahepatic gallstones were completely removed &#40;<a class="elsevierStyleCrossRef" href="#f0005">Figure 1D</a>&#41;&#46; The patient&#8217;s symptoms revolved&#46;</p><elsevierMultimedia ident="f0005"></elsevierMultimedia><p id="p0010" class="elsevierStylePara elsevierViewall">The location of the calculi in this patient suggested primary intrahepatic cholesterol gallstones rather than secondary intrahepatic stones due to migration from the gallbladder&#46; Variation of the anatomy of the bile ducts as a cause for intrahepatic cholelithiasis is controversial&#46; However&#44; some authors explain the predominance of intrahepatic gallstones in the left liver lobe with impaired bile flow due to the acute angle of the left hepatic duct&#46; In our case&#44; trifurcation of the hilus with an arcuated course of the segmental duct may have predisposed to primary intrahepatic stone formation in liver segment V only&#46;</p><p id="p0015" class="elsevierStylePara elsevierViewall">The young age of the patient with cholelithiasis&#44; recurrence of symptoms after cholecystectomy and intrahepatic calculi suggested the low phospholipid associated cholelithiasis &#40;LPAC&#41; syndrome&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Intrahepatic bile ducts filled with gallstones but no stricture as we found in our patient was recently described as one phenotype of the LPAC syndrome&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> In patients with LPAC&#44; the presumed low phospholipid concentration in bile is due to mutations of the <span class="elsevierStyleItalic">ABCB4</span> gene that encodes the phospholipid transporter MDR3 that is located on the canalicular membrane of hepatocytes and transport phospholipids into bile&#46; In this patient&#44; we did not examine bile under the polarizing light microscope&#44; measure phospholipid content in bile or&#44; to date&#44; sequence the <span class="elsevierStyleItalic">ABCB4</span> gene&#46; However&#44; in this subtype of the LPAC syndrome ursodeoxycholic acid was reported to be beneficial and we recommended therapy with ursodeoxycholic acid &#40;1&#44;000 mg&#47;day&#41; for dissolution of remaining microliths and prevention of recurrent disease&#46;</p></span></span>"
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Article information
ISSN: 16652681
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