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Literature DB >> 22379294

Hepatosplenic T-cell lymphoma.

Fahad I Alsohaibani¹, Maheeba A Abdulla, Mousa M Fagih.

Abstract

We report an uncommon case of 38-year-old male patient with Hepatosplenic T-Cell lymphoma (HSTCL) which is a rare aggressive form of Peripheral T-Cell lymphoma that is characterized by primary extranodal disease with malignant T-cell proliferation in the liver, spleen, and bone marrow. Our patient presented with progressive painless jaundice, weight loss and massive hepatosplenomegaly. The diagnosis was challenging as he required an extensive investigations that ultimately showed the characteristic clinical, histopathologic, and cytogenetic features of hepatosplenic T-cell lymphoma.

Entities: Disease Species

Keywords: Hepatosplenic; Hepatosplenomegaly; Lymphoma

Year: 2011 PMID： 22379294 PMCID： PMC3102508 DOI： 10.1007/s12288-010-0051-1

Source DB: PubMed Journal: Indian J Hematol Blood Transfus ISSN： 0971-4502 Impact factor: 0.900

17 in total

1. The World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues. Report of the Clinical Advisory Committee meeting, Airlie House, Virginia, November, 1997.

Authors: N L Harris; E S Jaffe; J Diebold; G Flandrin; H K Muller-Hermelink; J Vardiman; T A Lister; C D Bloomfield
Journal: Ann Oncol Date: 1999-12 Impact factor: 32.976

2. T gamma/delta hepatosplenic lymphoma in a heart transplant patient after an Epstein-Barr virus positive lymphoproliferative disorder: a case report.

Authors: M D Kraus; D F Crawford; Z Kaleem; S Shenoy; C A MacArthur; J A Longtine
Journal: Cancer Date: 1998-03-01 Impact factor: 6.860

3. Hepatosplenic alphabeta T-cell lymphomas: a report of 14 cases and comparison with hepatosplenic gammadelta T-cell lymphomas.

Authors: W R Macon; N B Levy; P J Kurtin; K E Salhany; M Y Elkhalifa; T T Casey; F E Craig; C L Vnencak-Jones; M L Gulley; J P Park; J B Cousar
Journal: Am J Surg Pathol Date: 2001-03 Impact factor: 6.394

4. Hepatosplenic T-cell lymphoma of alphabeta lineage in a 16-year-old boy presenting with hemolytic anemia and thrombocytopenia.

Authors: R Lai; L M Larratt; W Etches; S T Mortimer; L D Jewell; L Dabbagh; R W Coupland
Journal: Am J Surg Pathol Date: 2000-03 Impact factor: 6.394

Review 5. Hepatosplenic T cell lymphoma. A review on 45 cases since the first report describing the disease as a distinct lymphoma entity in 1990.

Authors: E Weidmann
Journal: Leukemia Date: 2000-06 Impact factor: 11.528

6. Hepatosplenic T-cell lymphoma: a distinct clinicopathologic entity of cytotoxic gamma delta T-cell origin.

Authors: C B Cooke; L Krenacs; M Stetler-Stevenson; T C Greiner; M Raffeld; D W Kingma; L Abruzzo; C Frantz; M Kaviani; E S Jaffe
Journal: Blood Date: 1996-12-01 Impact factor: 22.113

7. Hepatosplenic gamma-delta T-cell lymphoma: clinicopathological features and treatment.

Authors: G S Falchook; F Vega; N H Dang; F Samaniego; M A Rodriguez; R E Champlin; C Hosing; S Verstovsek; B Pro
Journal: Ann Oncol Date: 2009-02-23 Impact factor: 32.976

8. Consistent presence of isochromosome 7q in hepatosplenic T gamma/delta lymphoma: a new cytogenetic-clinicopathologic entity.

Authors: C C Wang; H F Tien; M T Lin; I J Su; C H Wang; S M Chuang; M C Shen; C H Liu
Journal: Genes Chromosomes Cancer Date: 1995-03 Impact factor: 5.006

Review 9. A revised European-American classification of lymphoid neoplasms: a proposal from the International Lymphoma Study Group.

Authors: N L Harris; E S Jaffe; H Stein; P M Banks; J K Chan; M L Cleary; G Delsol; C De Wolf-Peeters; B Falini; K C Gatter
Journal: Blood Date: 1994-09-01 Impact factor: 22.113

Review 10. Hepatosplenic gammadelta T-cell lymphoma is a rare clinicopathologic entity with poor outcome: report on a series of 21 patients.

Authors: Karim Belhadj; Felix Reyes; Jean-Pierre Farcet; Herve Tilly; Christian Bastard; Regis Angonin; Eric Deconinck; Frederic Charlotte; Veronique Leblond; Eric Labouyrie; Pierre Lederlin; Jean-Francois Emile; Beatrice Delmas-Marsalet; Bertrand Arnulf; Elie-Serge Zafrani; Philippe Gaulard
Journal: Blood Date: 2003-08-07 Impact factor: 22.113

5 in total

Hepatosplenic T-cell lymphoma.

1. The World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues. Report of the Clinical Advisory Committee meeting, Airlie House, Virginia, November, 1997.

2. T gamma/delta hepatosplenic lymphoma in a heart transplant patient after an Epstein-Barr virus positive lymphoproliferative disorder: a case report.

3. Hepatosplenic alphabeta T-cell lymphomas: a report of 14 cases and comparison with hepatosplenic gammadelta T-cell lymphomas.

4. Hepatosplenic T-cell lymphoma of alphabeta lineage in a 16-year-old boy presenting with hemolytic anemia and thrombocytopenia.

Review 5. Hepatosplenic T cell lymphoma. A review on 45 cases since the first report describing the disease as a distinct lymphoma entity in 1990.

6. Hepatosplenic T-cell lymphoma: a distinct clinicopathologic entity of cytotoxic gamma delta T-cell origin.

7. Hepatosplenic gamma-delta T-cell lymphoma: clinicopathological features and treatment.

8. Consistent presence of isochromosome 7q in hepatosplenic T gamma/delta lymphoma: a new cytogenetic-clinicopathologic entity.

Review 9. A revised European-American classification of lymphoid neoplasms: a proposal from the International Lymphoma Study Group.

Review 10. Hepatosplenic gammadelta T-cell lymphoma is a rare clinicopathologic entity with poor outcome: report on a series of 21 patients.

1. Hepatosplenic T cell lymphoma.

2. Hepatosplenic T Cell Lymphoma in an Immunocompetent Female Diagnosed using Flow Cytometry: A Rare Clinical Entity.

3. Hepatosplenic T-cell lymphoma in a young immunocompetent man.

4. Primary hepatic peripheral T-cell lymphoma associated with Epstein-Barr viral infection.

Review 5. Clinical, Diagnostic and Prognostic Characteristics of Primary Cutaneous Gamma Delta T-cell Lymphomas.