Introduction

Hepatoid adenocarcinoma (HAC) is a very rare finding, and generally occurs in the stomach, ovaries, and lungs. The term hepatoid adenocarcinoma was first introduced by Ishikura et al. in 1985 [1]. This report presents only the ninth case of HAC in the urinary bladder to be published in the literature, and reviews the previously reported cases.

Case presentation

A 49-year-old Japanese woman was diagnosed as having a breast tumor, and a total mastectomy was subsequently performed. A histology study of the breast tumor revealed a ductal carcinoma in situ with the pathological stage TisN0M0. A year after surgery, abdominal computed tomography (CT) revealed a mass lesion in the urinary bladder (Figure 1). There were no abnormal findings in the liver. Serological markers for hepatitis B and C viruses were also within normal limits. Cystoscopy revealed a solitary tumor on the left wall of the bladder (Figure 2). The tumor appeared to occur from the subepithelial tissue. Based on the findings, our patient was diagnosed as having a bladder tumor, therefore trans-urethral resection of the bladder tumor (TURBT) was performed. The tumor cells were microscopically typed as a hepatocellular carcinoma, featuring large, polygonal cells with marked nuclear atypia and eosinophilic granular or clear cytoplasma (Figure 3). Immunohistochemical staining test results were positive for α-fetoprotein (AFP) (Figure 4). A histology study of the tumor revealed a typical HAC, predominantly resembling a hepatocellular carcinoma. The tumor had spread to the subepithelial connective tissue below the non-atypical transitional epithelium, and the pathological stage was T1N0M0. After surgery, her serum AFP concentration was within normal limits. Chemotherapy was not administered. At 20 months after surgery, our patient has had no evidence of recurrence.

Figure 1
figure 1

Abdominal computed tomography showing a 6mm mass in the bladder.

Full size image
Figure 2
figure 2

Cystoscopy showing a solitary tumor on the left wall of the bladder.

Full size image
Figure 3
figure 3

Histopathological features of hepatoid adenocarcinoma of the urinary bladder. The tumor was composed of large, polygonal cells with eosinophilic cytoplasm. The cells were predominantly arranged in a trabecular pattern (hematoxylin and eosin stained specimen, ×100).

Full size image
Figure 4
figure 4

Immunohistochemical profile of hepatoid adenocarcinoma of the urinary bladder. Intra-cytoplasmic cells positive for α-fetoprotein, ×100.

Full size image

Discussion

HAC is a rare tumor, which is characterized by the morphological phenotype of a hepatocellular carcinoma. HAC is defined by the reproduction of a pattern similar to that of a hepatocellular carcinoma, with a combination of histopathological findings of solid nests and trabecular structures of polygonal atypical cells with wide granular cytoplasm and an immunochemical expression of AFP. Before a diagnosis of HAC is made, the metastases of a hepatocellular carcinoma should be ruled out.

Metzgeroth et al. recently published an evaluation of 262 HAC cases [2]. The stomach was the most common location with a frequency of 63 percent, followed by the ovaries (10 percent), lungs (4 percent), gallbladder (3 percent), pancreas (4 percent), uterus (4 percent), and urinary bladder (3 percent). HAC usually presents in older patients. The male to female ratio was 2.4:1 and the median age at diagnosis was 65 years (range 21 to 88 years). HAC is treated like other adenocarcinomas of the common type, depending on the organ system involved. The prognosis of HAC is considered to be unfavorable. HAC is regarded to be an aggressive neoplasm associated with a high proportion of metastases at the time of diagnosis. The lymph nodes, the liver and the brain are common metastatic sites. The survival rate of 83 cases with various HAC indicated 43 patients had died within the first 12 months, and 40 patients were alive for more than 12 months. The one-year survival rate (expressed as a percentage) was about 55 percent and the median overall period of survival was 11 months (range 0 to 102 months) [2].

The first case of HAC in the urinary bladder was reported by Sinard et al. in 1994 [3] and only eight cases have been reported to date [3–7]. The main clinical and pathological data from the previously reported cases are presented in Table 1[2–6]. As can be seen from the previous cases and our patient’s case, the patients were six men and three women. Their mean age was 68 years (range: 49 to 89 years). Hematuria was the initial symptom in six patients. Six cases received serum AFP examinations and five yielded positive results. However, HAC was not always accompanied by high levels of serum AFP [8]. Three cases were treated with cystectomies and six with TURBT. The pathological stages were T1 (n=3), T2 (n=3), and T3 (n=3). The prognosis of HAC was considered to be unfavorable, like that of other organs. Three patients underwent cystectomies and died of the disease 12 to 19 months later due to lung metastases. However, three cases of pT1 appeared to have been cured by TURBT and, post-operatively, they have had no evidence of recurrence more than 20 months later. The prolonged patient survival might be related to the low pathological stage of the tumor. Further studies with a large number of cases are required to classify the risk and management of HAC in the urinary bladder.

Table 1 Characteristics of patients with hepatoid adenocarcinoma (HAC) in the urinary bladder
Full size table

Conclusions

Hepatoid adenocarcinoma is a highly aggressive tumor mimicking the histological appearance of hepatocellular carcinoma. There are few reports describing hepatoid adenocarcinoma of the urinary bladder. It is important to be aware of atypical cancer localizations in order to reach a correct diagnosis.

Consent

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.