A case of congenital giant gallbladder with massive hydrops mimicking celiac cyst

  • Authors:
    • Liang Zong
    • Ping Chen
    • Lei Wang
    • Chunlan He
    • Guangyao Wang
    • Jian Jiang
    • Hao Wang
  • View Affiliations

  • Published online on: October 31, 2012     https://doi.org/10.3892/ol.2012.1010
  • Pages: 226-228
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Abstract

We present a case of a 55-year-old female who suffered from a mass in the right upper abdomen, which had been present for over six months. Pre-operative blood examinations, including tumor markers, were normal. Initially, the admitting diagnosis was a giant celiac cyst, due to its liquid cystic appearance and large size (approximately 30.0x18.0 cm), visible in the hepatic region under ultrasound. Following the discovery of a cystic duct during surgery, the diagnosis was corrected to be a giant gallbladder. As no obstructive matter was observed, the giant gallbladder was considered to be congenital.

Introduction

Large gallbladders are commonly present in biliary diseases, but reports of giant gallbladder are rare (14). Previous studies have revealed that a giant gallbladder was always accompanied with a tumor or gallstones. However, extremely large gallbladder with no marked obstructive factors such as biliary tumors and gallstones is considerably rarer. In this case report we present a rare case of a giant gallbladder that contained nothing but extremely large hydrops. This unique case may be useful in exploring the mechanisms involved in the development of giant gallbladders. Written informed consent was obtained from the patient’s family.

Case report

The patient was a 55-year-old female who complained of a mass in the right upper abdomen that had first appeared over six months previously. Prior to this, the patient had a 5-year-long history of abdominal distension. Until admission, the patient was well; she experienced epigastric discomfort due to compression, but did not experience a fever, vomiting, abdominal ache or jaundice. A physical examination revealed a large lump in the liver area on the right side of the rib cage. This continued down as far as the hip bone, but not past the mid-section, and the patient did not experience any notable tenderness. Routine blood test results, including hepatic function and renal function, were found to be normal. An abdominal ultrasound scan revealed a giant, liquid, dark area measuring 30.0×18.0 cm, visible in the hepatic region (Fig. 1). No abnormalities were revealed in the laboratory data, including the tumor markers that are listed in Table I.

Table I

Laboratory findings on admission.

Table I

Laboratory findings on admission.

Blood markersIndexNormal range
WBC (×109/l)10.14.0–10.0
RBC (×1012/l)3.73.5–5.0
BUN (mmol/l)5.63.2–6.0
Hemoglobin (g/l)113110–150
Hematocrit (vol%)4037–48
Platelets (×109/l)210100–300l
Total protein (g/l)6760–80
Albumin/globulin ratio1.21.1–2.5
Total bilirubin (μmol/l)11.25.7–23.5
Direct bilirubin (μmol/l)2.31.7–7.8
SGOT (U/l)370–50
SGPT (U/l)420–50
Total cholesterol (mmol/l)1.301.29–1.55
Serum amylase (U/l)6125–125
Lactic dehydrogenase (U/l)147.0135.0–215.0
Alkaline phosphatase (U/l)7625–150
CA19-9 (KU/l)5.47<35.00
CA242 (KU/l)1.31<20.00
CA125 (KU/l)2.27<35.00
CA15-3 (KU/l)2.28<35.00l
NSE (ng/ml)<1.0<13.00
CEA (ng/ml)1.21<5.00
Ferritin (ng/ml)27.13<219.00
Bta-HCG (MIU/ml)<0.02l<3.00
AFP (ng/ml)0.88<20.00
Free-PSA (ng/ml)<0.22<1.00
PSA (ng/ml)<0.04<5.00
HGH (ng/ml)2.15<7.50

A laparotomy was performed, during which an incision was made in the middle line, below the umbilicus. Initially, it was not possible to determine the point at which the sac originated, due to its large size of approximately 30.0×31.0×18.0 cm. The sac constituted almost half of the total epigastric region. Additionally, it was not possible to discern the layers of peritoneum and sac, owing to its very firm adhesion. As the uncertainty concerning the sac was so great, it was decided that the sac be emptied with a large trocar; approximately 3,800 ml of fluid was drained, leaving at least 200 ml in the bottom of the cyst. The diagnosis was corrected to be a giant gallbladder when a 4 mm slender cystic duct connecting to an 8 mm choledochus was discovered during the operation. As no obstructive matter, such as a tumor or gallstones were observed, this particular giant gallbladder was considered to be congenital. The pathological section revealed that columnar epithelium was present in the lining of the gallbladder wall along with inflammatory cell infiltration (Fig. 2A and B). Following the operation, there were no complications. The patient was treated and discharged after 10 days.

Discussion

A normal gallbladder is typically no more than 7.5–10 cm in length. However, it can present a considerably large size under the rare condition of genoconstitution. However, most gallbladders of extremely large size are correlated with pathological states, particularly in obstructive biliary diseases. The original study by Courvoisier et al stated that a growing, large gallbladder was more frequently caused by a biliary obstructive tumor such as a pancreatic malignancy, rather than gallstones, which may attribute to intraluminal hypertension over a shorter period of time (57). According to Courvoisier et al, a gallstone does not result in an enlarged gallbladder, as it is formed over an extended period of time, resulting in a shrunken, fibrotic and scarred gallbladder that does not allow extended enlargement. However, an exception to Courvoisier’s law supports the theory that the stones may be responsible for a growing, large gallbladder. This theory suggests that the stones may dislodge and acutely block the duct distally to the hepatic/cystic duct junction, contributing to the action of check valves. In a review of published work (1), such cases of a giant gallbladder combined with gallstones can be further explained by this theory of etiology.

The case we present here was unique, owing to the unusually large size of the gallbladder, being amongst the largest found in a review of the literature (Table II). Moreover, no obstructive factors, such as a tumor or stones, were present. However, the biliary duct was fluent, which enabled bile to freely enter the intestinal tract. As neither marked biliary inflammation nor biliary obstruction was observed, this particular giant gallbladder was considered to be congenital. With the progression of the disease, the giant gallbladder became increasingly filled with bile, which lead to chronic inflammation that subsequently damaged the contractile function of the gallbladder and contributed to further growth of the congenital large gallbladder.

Table II

Overview of the reported cases of giant gallbladder.

Table II

Overview of the reported cases of giant gallbladder.

Authors (Ref.)GenderAge (years)Size (cm)ObstructionPost-operative diagnosis
Grosberg (1)Female9514×5.5StoneAcute gangrenous cholecystitis, cholelithiasis
Maeda et al(2)Female3618×4NoChronic cholecystitis, cholelithiasis
Hsu et al(3)Female8716.4×13.6×7.8NoAcute cholecystitis, gall bladder adenocarcinoma
Panaro et al(4)NA1743×21×20NoByler’s disease

[i] NA, not available.

References

1 

Grosberg SJ: Giant gallbladder. Am J Dig Dis. 7:1039–1040. 1962. View Article : Google Scholar

2 

Maeda Y, Setoguchi T, Yoshida T, et al: A giant gallbladder. Gastroenterol Jpn. 14:621–624. 1979.

3 

Hsu KF, Yeh CL, Shih ML, et al: Giant gallbladder: adenocarcinoma complicated with empyema. J Trauma. 70:2612011. View Article : Google Scholar : PubMed/NCBI

4 

Panaro F, Chastaing L and Navarro F: Education and imaging. Hepatobiliary and pancreatic: giant gallbladder associated with Byler’s disease. J Gastroenterol Hepatol. 27:6202012.PubMed/NCBI

5 

Hagege A: Case of retention jaundice; importance of Courvoisier-Terrier law. Tunis Med. 45:4391957.(In French).

6 

Watts GT: Courvoisier’s law. Lancet. 2:1293–1294. 1985.

7 

Verghese A and Berk SL: Courvoisier’s law. Lancet. 1:991986.

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Spandidos Publications style
Zong L, Chen P, Wang L, He C, Wang G, Jiang J and Wang H: A case of congenital giant gallbladder with massive hydrops mimicking celiac cyst. Oncol Lett 5: 226-228, 2013
APA
Zong, L., Chen, P., Wang, L., He, C., Wang, G., Jiang, J., & Wang, H. (2013). A case of congenital giant gallbladder with massive hydrops mimicking celiac cyst. Oncology Letters, 5, 226-228. https://doi.org/10.3892/ol.2012.1010
MLA
Zong, L., Chen, P., Wang, L., He, C., Wang, G., Jiang, J., Wang, H."A case of congenital giant gallbladder with massive hydrops mimicking celiac cyst". Oncology Letters 5.1 (2013): 226-228.
Chicago
Zong, L., Chen, P., Wang, L., He, C., Wang, G., Jiang, J., Wang, H."A case of congenital giant gallbladder with massive hydrops mimicking celiac cyst". Oncology Letters 5, no. 1 (2013): 226-228. https://doi.org/10.3892/ol.2012.1010