Hepatobiliary and Pancreatic: Hepatosplenic gamma-delta T-cell lymphoma
Article first published online: 21 DEC 2011
© 2011 Journal of Gastroenterology and Hepatology Foundation and Blackwell Publishing Asia Pty Ltd
Journal of Gastroenterology and Hepatology
Volume 27, Issue 1, page 184, January 2012
How to Cite
Qi, X., Han, G., He, C., Guo, W. and Fan, D. (2012), Hepatobiliary and Pancreatic: Hepatosplenic gamma-delta T-cell lymphoma. Journal of Gastroenterology and Hepatology, 27: 184. doi: 10.1111/j.1440-1746.2011.06983.x
- Issue published online: 21 DEC 2011
- Article first published online: 21 DEC 2011
Hepatosplenic gamma-delta (γδ) T-cell lymphoma is a rare form of peripheral T-cell lymphoma that was first proposed as a distinct clinicopathologic entity in 1990. Common presenting symptoms include fever, weakness and abdominal pain. On examination, the liver and spleen are enlarged but there are no enlarged peripheral lymph nodes. Typical blood tests reveal anemia, leukopenia and thrombocytopenia but liver function tests are either normal or near-normal. Histological features are characterized by malignant T-cell proliferation in the sinusoids of the liver, sinuses and red pulp of the spleen and sinuses of the bone marrow. Immunophenotypic expressions include CD2+, CD3+, CD4-, CD5±, CD7±, CD16±, CD56±, TIA-1+, TdT- and granzyme B±. The T-cell receptor—γδ phenotype (TCRδ1+) is positive while the T-cell receptor—αβ phenotype (βF1) is negative. Thus far, responses to chemotherapeutic regimens have been poor and patients have a median survival of only 11–16 months. Of interest to gastroenterologists are case reports of hepatosplenic γδ T-cell lymphomas in patients with inflammatory bowel disease after treatment with monoclonal antibodies against tumor necrosis factor. Most of these patients have been young men receiving concomitant medication with azathioprine, 6-mercaptopurine or methotrexate.
The patient illustrated below was a 46-year-old man who was admitted to hospital with upper abdominal distension and peripheral edema. Twelve months previously, he had been treated by splenectomy for splenomegaly and features of hypersplenism. An abdominal computed tomography scan showed a huge liver that extended into the pelvis. The liver had a heterogeneous appearance but no discrete nodules (Figure 1). Blood tests revealed mild anemia (hemoglobin 108 g/l), a mild elevation of the white cell count (13.4x109/l) and a low platelet count (40x109/l). The differential count of white cells showed an increase in monocytes (24%). Liver function tests were normal apart from an elevated serum bilirubin (46 µmol/l) and a low albumin (25 g/l). A liver biopsy revealed an infiltrate of lymphoid cells in the liver sinusoids (Figure 2 left) and positive histochemical stains for CD3 (Figure 2 right), CD56 and TIA-1. Lymphocytes were positive for the T-cell receptor γδ and strongly positive for Ki-67. The findings were typical of hepatosplenic γδ T-cell lymphoma.