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Regression Of Hodgkin Lymphoma After Discontinuation Of A Tumor Necrosis Factor Inhibitor For Crohn's Disease: A Case Report And Review Of The Literature

Cassaday et al., 2011Lymphoma

Cassaday, R. D., Malik, J. T., & Chang, J. E. (2011). Regression of Hodgkin lymphoma after discontinuation of a tumor necrosis factor inhibitor for Crohn's disease: a case report and review of the literature. Clinical lymphoma, myeloma & leukemia, 11(3), 289–292. https://doi.org/10.1016/j.clml.2011.03.018

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Abstract

Lymphoma is an increasingly recognized complication of tumor necrosis factor (TNF) inhibition for the treatment of autoimmune and inflammatory disease; the majority of these cases are non-Hodgkin lymphomas (NHL). The impact of withdrawing TNF inhibition therapy in cases of lymphoma is not well described. A woman with Crohn's disease (CD) was diagnosed with Hodgkin lymphoma (HL) and subsequently went into remission with standard chemotherapy. Her CD later worsened, requiring initiation of adalimumab, a TNF inhibitor. Ten months later, she was found to have recurrence of HL. When she opted against additional treatment for the lymphoma, the TNF inhibitor was discontinued. Three months later, the measurable sites of disease had completely regressed. It can be concluded that HL is a potential complication of treatment with TNF inhibitors. Withdrawal of immunosuppression may be a consideration for patients treated for lymphoproliferative disorders including HL. Maintenance of an intact immune system may be important for prevention of lymphoma relapse. Further understanding of this complex interaction will help clinicians determine in which patients these agents have a favorable risk-benefit ratio.

Case Details

Disease Location

Intra-abdominal liver and spleen

Personal Characteristics

54 -year-old female history of crohn's disease, diagnosed 16 years before hl

Clinical Characteristics

Diagnosed with nodular sclerosing hl after cervical lymphadenopathy was indentified during parathyroidectomy for surgical management of primary hyperparathyroidism excisional ln biopsy confirmed reed-sternberg cells, which were positive for CD30 & 15, and negative for CD3, 20, 45,and cyclin d1. Positive results for epstein-barr-encoded RNA (eber). CT scan for staging evaluation confirmed stage iiia disease 10 months after adalimumab was started, she admitted with abdominal pain, diarrhea and fever. CT showed intra-abdominal lymphadenopathy and multiple hypodense lesions in the liver and spleen liver biopsy confirmed recurrent nodular sclerosing hl, morphologic and immunophenotypic features were similar to findings from initial diagnosis with the exception of negative eber immunostaining. Refused additional chemo and referral was made for home hospice 2 months after the 3 months follow-up, had recurrent abdominal pain and fever which were attributed to cholecystitis base on inflammatory gallbladder changes on ultrasonographic imaging. Underwent cholecystectomy and liver biopsy during the operation, probable abscess near the hilum of the liver was noted and a percutaneous drain was placed, liver biopsy showed evidence of residual hl but imaging at that time showed no gross residual disease post-op was complicated by a retroperitoneal hematoma and her condition deteriorated and died 20 days after the operation

Remission Characteristics

Achieved complete remission with stanford v therapy 3 months after discharge, CT revealed resolution of liver and spleen lesions and the multiple abdominal lymphadenopathy

Treatment & Mechanisms

Proposed Remission Mechanisms

Withdrawal of adalimumab therapy

Clinical Treatment

3 cycles of stanford v regimen m started adalimumab appx 1 year after chemotherapy underwent multiple bowel resections and was receiving chronic steroid treatment and azathioprine at the time of hl diagnosis when discharge with hospice referral, patient was given prednisone for gi symptoms open cholecystectomy

Non-Clinical Treatment

None reported