Hepatosplenic T-cell lymphoma
|Hepatosplenic T-cell lymphoma|
|Classification and external resources|
|Please help improve this article by expanding it. Further information might be found on the talk page. (December 2009)|
Hepatosplenic γδ T-cell lymphoma
The cell of origin for this disease is an immature cytotoxic T-cell clonally expressing the γδ T-cell receptor. This disease is seen more often in immunosuppressed solid organ transplant recipients, an association that has led to the hypothesis that long-term immune stimulation in the setting of immunosuppression is the causative agent.
The constellation of thrombocytopenia, anemia, and leukocytosis is common in patients with hepatosplenic T-cell lymphoma. The discovery of neoplastic cells in peripheral blood is often a finding late in the clinical course.
Sites of Involvement
Spleen and liver
While the bone marrow is commonly involved, the detection of the neoplastic infiltrate may be difficult due to diffuse, interstitial pattern. Immunohistochemistry can aid in the detection of this lymphoma.
|Positive||CD3, TCRδ1, TIA-1|
|Negative||CD4, CD5, CD8|
Clonal rearrangement of the γ gene of the T-cell receptor is the hallmark of this disease. A few cases have shown rearrangement of the T-cell receptor β gene. Isochromosome 7q has been observed in all cases described so far, sometimes in conjunction with other chromosomal abnormalities such as trisomy 8.
CHOP-R frequently induces remission initially, but most patients relapse and die within 2 years. Autologus bone marrow transplantion is currently being investigated in the treatment of hepatosplenic lymphoma.
- ↑ Mackey AC, Green L, Liang LC, Dinndorf P, Avigan M (February 2007). "Hepatosplenic T cell lymphoma associated with infliximab use in young patients treated for inflammatory bowel disease". J. Pediatr. Gastroenterol. Nutr. 44 (2): 265–7. doi:10.1097/MPG.0b013e31802f6424. PMID 17255842. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?an=00005176-200702000-00019.
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 2.9 Elaine Sarkin Jaffe, Nancy Lee Harris, World Health Organization, International Agency for Research on Cancer, Harald Stein, J.W. Vardiman (2001). Pathology and genetics of tumours of haematopoietic and lymphoid tissues. World Health Organization Classification of Tumors. 3. Lyon: IARC Press. ISBN 92-832-2411-6. http://books.google.com.au/books?id=XSKqcy7TUZUC.
- ↑ 3.0 3.1 3.2 3.3 3.4 Cooke CB, Krenacs L, Stetler-Stevenson M, et al. (December 1996). "Hepatosplenic T-cell lymphoma: a distinct clinicopathologic entity of cytotoxic gamma delta T-cell origin". Blood 88 (11): 4265–74. PMID 8943863. http://www.bloodjournal.org/cgi/pmidlookup?view=long&pmid=8943863.
- ↑ Ross CW, Schnitzer B, Sheldon S, Braun DK, Hanson CA (September 1994). [Expression error: Missing operand for > "Gamma/delta T-cell posttransplantation lymphoproliferative disorder primarily in the spleen"]. Am. J. Clin. Pathol. 102 (3): 310–5. PMID 8085554.
- ↑ Macon WR, Levy NB, Kurtin PJ, et al. (March 2001). "Hepatosplenic alphabeta T-cell lymphomas: a report of 14 cases and comparison with hepatosplenic gammadelta T-cell lymphomas". Am. J. Surg. Pathol. 25 (3): 285–96. doi:10.1097/00000478-200103000-00002. PMID 11224598. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0147-5185&volume=25&issue=3&spage=285.
- ↑ Farcet JP, Gaulard P, Marolleau JP, et al. (June 1990). "Hepatosplenic T-cell lymphoma: sinusal/sinusoidal localization of malignant cells expressing the T-cell receptor gamma delta". Blood 75 (11): 2213–9. PMID 2140703. http://www.bloodjournal.org/cgi/pmidlookup?view=long&pmid=2140703.
- ↑ Alonsozana EL, Stamberg J, Kumar D, et al. (August 1997). [Expression error: Missing operand for > "Isochromosome 7q: the primary cytogenetic abnormality in hepatosplenic gammadelta T cell lymphoma"]. Leukemia 11 (8): 1367–72. doi:10.1038/sj.leu.2400742. PMID 9264394.