Hepatosplenic Gamma Delta T-Cell Lymphoma (HSGDTCL): Two Rare Case Reports from Western India

Peripheral T cell lymphomas are a heterogeneous group of post-thymic, mature lymphoid malignancies, accounting for approximately 10-15% of all non-Hodgkin's lymphomas. Hepatosplenic T-cell lymphoma (HSGDTCL) is a rare entity, which is characterized by primary extra nodal disease with typical s...

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Main Authors: Irappa Madabhavi, Gaurang Modi, Harsha Panchal, Apurva Patel, Swaroop Revannasiddaiah, Asha Anand, Sonia Parikh, Kshitij Joshi, Malay Sarkar
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2017-10-01
Series:International Journal of Hematology-Oncology and Stem Cell Research
Subjects:
Online Access:https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/372
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spelling doaj-5cb278878ef94758b5602341899e940d2020-11-25T04:08:31ZengTehran University of Medical SciencesInternational Journal of Hematology-Oncology and Stem Cell Research2008-22072017-10-01114Hepatosplenic Gamma Delta T-Cell Lymphoma (HSGDTCL): Two Rare Case Reports from Western IndiaIrappa Madabhavi0Gaurang Modi1Harsha Panchal2Apurva Patel3Swaroop Revannasiddaiah4Asha Anand5Sonia Parikh6Kshitij Joshi7Malay Sarkar8Department of Medical and Pediatric Oncology, GCRI, Ahmedabad, Gujarat, IndiaDepartment of Medical and Pediatric Oncology, GCRI, Ahmedabad, Gujarat, IndiaDepartment of Medical and Pediatric Oncology, GCRI, Ahmedabad, Gujarat, IndiaDepartment of Radiotherapy, Government Medical College, Haldwani, Uttarakhand, IndiaDepartment of Medical and Pediatric Oncology, GCRI, Ahmedabad, Gujarat, IndiaDepartment of Medical and Pediatric Oncology, GCRI, Ahmedabad, Gujarat, IndiaDepartment of Medical and Pediatric Oncology, GCRI, Ahmedabad, Gujarat, IndiaDepartment of Pulmonary Medicine, IGMC, Shimla, Himachal Pradesh, IndiaDepartment of Pulmonary Medicine, IGMC, Shimla, Himachal Pradesh, India Peripheral T cell lymphomas are a heterogeneous group of post-thymic, mature lymphoid malignancies, accounting for approximately 10-15% of all non-Hodgkin's lymphomas. Hepatosplenic T-cell lymphoma (HSGDTCL) is a rare entity, which is characterized by primary extra nodal disease with typical sinusoidal or sinusal infiltration of the liver and the spleen, respectively by expression of the T cell receptor   chain, and by a number of other frequent clinicopathologic features, including aggressive course of disease. Secondary involvement of liver by hematopoietic malignancies is much more common as compared to primary liver involvement. Primary involvement of liver by non- Hodgkin’s lymphoma (NHL) is documented and mostly DLBCL (diffuse large B cell lymphoma) type.  But, T cell lymphoma primarily arising from liver is very rare. It occurred commonly in immunocompromised patients and prognosis is very poor. Here, we present two case reports of Hepatosplenic gamma-delta T-cell lymphoma (HSGDTCL) and both are immunocompetent patients. Liver biopsy from the mass and subsequent IHC (immunohistochemistry) were performed for the purpose of diagnosis, which were positive for LCA (leukocyte common antigen), CD2 and negative for CD5, CD20 and CD79a. First patient was a 63-year-old female with hepatitis C virus seropositivity presented with liver mass simulating hepatocellular carcinoma.  Second patient was a 60-year- old male, chronic alcoholic patient, presented with liver mass and lytic bony lesion in pelvis. Both patients were managed with conventional CHOP (cyclophosphamide, hydroxydaunorubicin, vincristine, and prednisolone) and showed complete response after 4 cycles of chemotherapy. After completion of 6 cycles of chemotherapy, both patients remained under 6-month surveillance period for any recurrence of the disease. https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/372Hepatosplenic gamma delta T cell lymphoma (HSGDTCL)Immuno competent patientsCHOP
collection DOAJ
language English
format Article
sources DOAJ
author Irappa Madabhavi
Gaurang Modi
Harsha Panchal
Apurva Patel
Swaroop Revannasiddaiah
Asha Anand
Sonia Parikh
Kshitij Joshi
Malay Sarkar
spellingShingle Irappa Madabhavi
Gaurang Modi
Harsha Panchal
Apurva Patel
Swaroop Revannasiddaiah
Asha Anand
Sonia Parikh
Kshitij Joshi
Malay Sarkar
Hepatosplenic Gamma Delta T-Cell Lymphoma (HSGDTCL): Two Rare Case Reports from Western India
International Journal of Hematology-Oncology and Stem Cell Research
Hepatosplenic gamma delta T cell lymphoma (HSGDTCL)
Immuno competent patients
CHOP
author_facet Irappa Madabhavi
Gaurang Modi
Harsha Panchal
Apurva Patel
Swaroop Revannasiddaiah
Asha Anand
Sonia Parikh
Kshitij Joshi
Malay Sarkar
author_sort Irappa Madabhavi
title Hepatosplenic Gamma Delta T-Cell Lymphoma (HSGDTCL): Two Rare Case Reports from Western India
title_short Hepatosplenic Gamma Delta T-Cell Lymphoma (HSGDTCL): Two Rare Case Reports from Western India
title_full Hepatosplenic Gamma Delta T-Cell Lymphoma (HSGDTCL): Two Rare Case Reports from Western India
title_fullStr Hepatosplenic Gamma Delta T-Cell Lymphoma (HSGDTCL): Two Rare Case Reports from Western India
title_full_unstemmed Hepatosplenic Gamma Delta T-Cell Lymphoma (HSGDTCL): Two Rare Case Reports from Western India
title_sort hepatosplenic gamma delta t-cell lymphoma (hsgdtcl): two rare case reports from western india
publisher Tehran University of Medical Sciences
series International Journal of Hematology-Oncology and Stem Cell Research
issn 2008-2207
publishDate 2017-10-01
description Peripheral T cell lymphomas are a heterogeneous group of post-thymic, mature lymphoid malignancies, accounting for approximately 10-15% of all non-Hodgkin's lymphomas. Hepatosplenic T-cell lymphoma (HSGDTCL) is a rare entity, which is characterized by primary extra nodal disease with typical sinusoidal or sinusal infiltration of the liver and the spleen, respectively by expression of the T cell receptor   chain, and by a number of other frequent clinicopathologic features, including aggressive course of disease. Secondary involvement of liver by hematopoietic malignancies is much more common as compared to primary liver involvement. Primary involvement of liver by non- Hodgkin’s lymphoma (NHL) is documented and mostly DLBCL (diffuse large B cell lymphoma) type.  But, T cell lymphoma primarily arising from liver is very rare. It occurred commonly in immunocompromised patients and prognosis is very poor. Here, we present two case reports of Hepatosplenic gamma-delta T-cell lymphoma (HSGDTCL) and both are immunocompetent patients. Liver biopsy from the mass and subsequent IHC (immunohistochemistry) were performed for the purpose of diagnosis, which were positive for LCA (leukocyte common antigen), CD2 and negative for CD5, CD20 and CD79a. First patient was a 63-year-old female with hepatitis C virus seropositivity presented with liver mass simulating hepatocellular carcinoma.  Second patient was a 60-year- old male, chronic alcoholic patient, presented with liver mass and lytic bony lesion in pelvis. Both patients were managed with conventional CHOP (cyclophosphamide, hydroxydaunorubicin, vincristine, and prednisolone) and showed complete response after 4 cycles of chemotherapy. After completion of 6 cycles of chemotherapy, both patients remained under 6-month surveillance period for any recurrence of the disease.
topic Hepatosplenic gamma delta T cell lymphoma (HSGDTCL)
Immuno competent patients
CHOP
url https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/372
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