High‐dose intravenous methotrexate followed by autologous stem cell transplantation as a potentially effective therapy for neurolymphomatosis

BACKGROUND Neurolymphomatosis (NL) is a rare neurologic manifestation of systemic lymphoma characterized by lymphomatous infiltration of the peripheral nervous system. The diagnosis of NL is difficult and requires a multidisciplinary approach for obtaining an adequate biopsy specimen of the suspecte...

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Veröffentlicht in:Cancer 2004-06, Vol.100 (11), p.2403-2407
Hauptverfasser: Ghobrial, Irene M., Buadi, Francis, Spinner, Robert J., Colgan, Joseph P., Wolanskyj, Alexandra P., Dyck, P. James, Witzig, Thomas E., Micallef, Ivana N., O'Neill, Brian Patrick
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Sprache:eng
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Zusammenfassung:BACKGROUND Neurolymphomatosis (NL) is a rare neurologic manifestation of systemic lymphoma characterized by lymphomatous infiltration of the peripheral nervous system. The diagnosis of NL is difficult and requires a multidisciplinary approach for obtaining an adequate biopsy specimen of the suspected nerve. The prognosis of patients with NL has been poor because adequate penetration of chemotherapy into the nervous system is difficult. METHODS The authors presented the case of a 37‐year‐old man who was treated for Ann Arbor Stage IVB diffuse large B‐cell lymphoma. The patient developed disease recurrence in the sciatic nerve without systemic involvement. RESULTS The patient achieved a clinical response after receipt of high‐dose intravenous methotrexate followed by high‐dose chemotherapy and autologous stem cell transplant. CONCLUSIONS The authors reported this case to highlight the effectiveness of this regimen in a rare and fatal disorder. In the current study they also reviewed the literature regarding the diagnosis, prognosis, and treatment of NL. Cancer 2004. © 2004 American Cancer Society. In the current study, the authors present a case from their own experience and review the literature regarding the diagnosis, prognosis, and treatment of patients with neurolymphomatosis.
ISSN:0008-543X
1097-0142
DOI:10.1002/cncr.20263