Osteoclast-Like Giant Cell Tumor Of The Liver: A Case Report And Literature Review

摘要

Osteoclast-like giant cell tumor (OGCT) of the liver is a rare tumor; only eight cases have been reported in the western literature. Herein is a review of the clinical and histological presentations of nine cases of OGCT; the ninth case is derived from an autopsy at our institution. The histological findings include benign multinucleate giant cells, and malignant pleomorphic mononuclear cells, with or without the classic hepatocellular carcinoma cells. The giant cells have a reactive nature akin to the giant cells associated with giant cell tumor of the bone, and they are positive for CD-68 and are nonreactive with cytokeratin and epithelial membrane antigen (EMA). The mononuclear cells are positive for cytokeratin and EMA but are negative for CD-68. The mononuclear cells can have sarcomatoid morphology. In our case, we observed multinucleate cells in association with the primary lesion and lung metastasis but not in the lymph node metastasis. Osteoclast-like giant cell tumors are rare tumors and have been reported in many organs, including ovary1, pancreas2, and urinary tract3. Only eight cases of osteoclast-like giant cell tumor (OGCT) of the liver have been reported in the western literature, most of which have consisted of biopsies or resection specimens with limited clinical and histologic information. Report of A Case A 65 year-old male presented with general weakness and right upper quadrant pain for two weeks. He had a past medical history of hepatitis C, liver cirrhosis, diabetes mellitus, and congestive heart failure. On physical examination, he had jaundice, abdominal distension and hepatomegaly. The significant laboratory findings included blood glucose 320 grams/dL, total bilirubin 2.7 mg/dL, GGT 122 U/dL, AST 97 U/dL, LDH 1156 u/dL, markedly elevated AFP 24,179 ng/dL, positive antibody for hepatitis C, and negative serology for hepatitis B. A CT scan at that time showed a large mass in the right hepatic lobe measuring 9.0 cm in greatest diameter. The diagnosis of hepatocellular carcinoma was rendered clinically; however, the patient was lost to follow-up before a tissue biopsy could be performed. One month later, due to increasing abdominal discomfort, the patient visited the emergency room, and a repeat CT showed significant enlargement of the liver mass and increasing ascites. The patient was admitted and an ultrasound guided biopsy was planned. Five days after admission, he suddenly developed hypovolemic shock and expired in spite of resuscitative measures. Pathologic Findings A complete autopsy was performed. The patient's abdomen was tense and markedly distended; it measured 147 cm in circumference. More than five liters of bloody fluid and blood clots were found in the peritoneal cavity. A ruptured, large, necrotic hepatic mass located in the right lobe of the liver measured 13 x 12 x 12 cm. The rupture and massive bleeding were the direct cause of the sudden death. Several necrotic satellite nodules were noted around the main mass. Tumor thrombi were present in the portal and hepatic veins. Many regional lymph nodes were enlarged and grossly replaced by tumor. Bilateral lungs showed necrotic metastases. Other organs were not involved by metastatic lesions. The rest of the liver was cirrhotic, and the 370 gram enlarged spleen showed passive congestion.Microscopic examination of the liver confirmed the macronodular cirrhosis. The majority of the sections from the hepatic mass showed extensive coagulative necrosis and tumor ghost cells and a few viable foci composed of benign osteoclast-like giant cells with abundant eosinophilic cytoplasm and a variable number of nuclei, mixed with malignant pleomorphic mononuclear cells (Figure 1. a).