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Adenocarcinoma of Gall Bladder

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Carcinoma of Gall Bladder ; Adenocarcinoma of Gall Bladder ; Papillary Adenocarcinoma of Gall Bladder ; Intestinal-type Adenocarcinoma of Gall Bladder ; Mucinous Adenocarcinoma of Gall Bladder ; Signet Ring Carcinoma of Gall Bladder; Clear Cell Adenocarcinoma of Gall Bladder ; Squamous/Adenosquamous Cell Carcinoma of Gall Bladder ;Small (oat) Cell Carcinoma of the Gall Bladder.

The most common tumour of the gall bladder is adenocarcinoma.

Although it is not one of the more frequent cancers, it is not rare, being incidentally found in 2% of patients who undergo gallbladder surgery.

Because this cancer is usually associated with cholelithiasis and chronic cholecystitis, it is considerably more common in women than men. Populations that have a high incidence of cholelithiasis, have a high risk of carcinoma of the gallbladder.

Adenocarcinomas account for 90% of gallbladder carcinomas and are characterized by glands lined by cuboidal or columnar cells, which may contain mucin.

They may be well, moderately, or poorly differentiated, depending on the degree of gland formation.  

There are several histologic variants of adenocarcinoma recognized: papillary, intestinal, mucinous, signet-ring cell, and clear cell. Many tumours contain more than one histologic variant.

Symptoms produced by the tumour are similar to those encountered with gallstone disease.

However, by the time the tumour becomes symptomatic, it is almost invariably incurable, the 5-year survival rate being less than 3%.

For practical purposes, surgical cure is obtained only in patients who undergo cholecystectomy for gallbladder disease and in whom the cancer is an accidental finding.

                     

Expression of nm23 and KAI1 and their clinical significance in gallbladder adenocarcinoma. Zhonghua Zhong Liu Za Zhi. 2008 Jun;30(6):441-3.

OBJECTIVE: To investigate the expression of two tumor metastasis suppressor genes nm23 and KAI1 in gallbladder adenocarcinoma, and their clinicopathological significance. METHODS: Specimens and clinical data from 31 gallbladder adenocarcinoma patients were collected. Histopathological grading and the expression of nm23 and KAI1 were detected by HE and immunohistochemical staining, respectively. All cases were followed up for at least three years. RESULTS: Immunohistochemical staining showed that the positive rate of nm23 and KAI1 proteins was 71.0% (22/31) and 61.3% (19/31), respectively. The positive expression rates of nm23 and KAI1 proteins in the early stage carcinomas were significantly higher than those in the moderate and advanced stage ones (P exact = 0.0051 and P exact = 0.0084), and both had an negative correlation with clinicopathologic stage (P trend = 0.0047 and P trend = 0.0058). There was a significant difference in the expression of nm23 and KAI1 proteins among well, moderately and poorly differentiated carcinomas (P exact = 0.0328 and P exact = 0.0020). The expression of nm23 and KAI1 was positively correlated with histopathological grade (P trend = 0.0086 and P trend = 0.0006). There was also a significant difference in the expression of nm23 and KAI1 proteins between 17 survival and 14 dead patients (P exact = 0.0038 and P exact = 0.0001 ). A synergistic effect of nm23 and KAI1 protein on the survival was observed , and seemed to be more important than any individual gene alone (P exact = 0.0005). CONCLUSION: The expressions of nm23 and KAI1 proteins are negatively correlated with clinical stage, but positively with histopathological grade in gallbladder adenocarcinoma. These two tumor metastasis suppressor genes may act synergistically to inhibit the tumor metastasis.

Clinicopathologic features of gallbladder adenocarcinoma with marked stromal fibrosis--a report of 19 cases. Ai Zheng. 2006 Jul;25(7):896-900.

BACKGROUND & OBJECTIVE: Macropathologic types of gallbladder cancer are mostly polyp type, intumescent type, and cauliflower form lump. Its histological types include well or poorly differentiated adenocarcinoma, mucinous adenocarcinoma, and undifferentiated cancer. This research was to explore the clinicopathologic features of gallbladder adenocarcinoma with marked stromal fibrosis. METHODS: Pathology of 19 cases of gallbladder adenocarcinoma with marked stromal fibrosis was observed using a light microscopy and SP immunohistochemistry. Clinicopathologic features of 19 patients were analyzed. RESULTS: Most of the patients had long-term history of cholecystitis gallbladder calculus. B ultrasound showed that the gallbladder wall was irregularly thickened or presented nodosity. Observed with naked eyes, gallbladder adenocarcinoma with marked stromal fibrosis did not form cancer nodule and extrude into the gallbladder lumen, the gallbladder wall showed regional thickening, a few cases showed diffuse irregular thickening. Observed under a light microscope, the adenocarcinoma cells were mostly arranged as single layers, seldom arranged as multiple layers, and formed adenoid structures with different sizes, various shapes, and irregular arrangement; the nuclei were heterogenic with haryomitosis presented in a few cases; inflammatory cells were infiltrated in hyperplastic fibrous connective tissue of some cases. According to immune phenotyping, CK (AE1/AE3), CK (AE1), CK7 (OV-TL12/30), CK8 (C51), CK18 (Dc-10), CK19 (RCK108), and EMA (Mc-5) showed strong expression, CEA (COL-1), CK20 (Ks20. 4), and MUC-5AC (CLH2) showed moderate expression, and MUC-2 (B306. 1) showed weak expression; CK17 (E3) showed focal expression. CONCLUSIONS: The clinical manifestation, macropathologic type, histological characteristics of gallbladder adenocarcinoma with stromal fibrosis are different from other types of adenocarcinoma. Its genesis may be related to chronic cholecystitis: long-term inflammation causes regional hyperplasia and heterogeneity of the gland body, lead to focal or regional thickening of the gallbladder wall, and result in gallbladder adenocarcinoma with stromal fibrosis finally.

 
July 2009   
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