PEDIATRICS Vol. 116 No. 6 December 2005, pp. e876-e879 (doi:10.1542/peds.2005-1068)
ELECTRONIC ARTICLE |
Cerebral Lymphoma in an Adenosine DeaminaseDeficient Patient With Severe Combined Immunodeficiency Receiving Polyethylene GlycolConjugated Adenosine Deaminase

* Department of Pediatrics, Louisiana State University Health Sciences Center, Shreveport, Louisiana
Department of Biochemistry, Duke University Medical Center, Durham, North Carolina
Polyethylene glycolconjugated adenosine deaminase (PEG-ADA) provides an alternate therapy to mismatched stem cell transplantation for patients with ADA-deficient severe combined immunodeficiency. Although replacement therapy with PEG-ADA is effective in preventing infections, immune function does not return to normal, and most patients remain lymphopenic. Information is limited regarding the prognosis of patients on long-term ADA-replacement therapy. Here we present a case of a 10-year-old child who was diagnosed with ADA-severe combined immunodeficiency at 4 weeks of age after contracting pneumonia. Treatment with PEG-ADA was begun, the biochemical markers of ADA deficiency normalized, and his clinical progress was very good without significant infections. At 10 years of age, after presenting with headaches and cranial nerve deficits, he was diagnosed with Epstein-Barr viruspositive malignant brain lymphoma. It did not respond to various regimens of aggressive chemotherapy, and the patient expired 5 months later. We speculate that in this patient the immunologic surveillance by T cells may have been defective with respect to elimination of Epstein-Barr virusinfected cells, hence the formation of neoplasm. The possible mechanisms underlying such pathology are reviewed.
Key Words: immunodeficiency severe combined immunodeficiency ADA deficiency PEG-ADA lymphoma
Abbreviations: SCID, severe combined immunodeficiency ADA, adenosine deaminase EBV, Epstein-Barr virus PEG, polyethylene glycol BMT, bone marrow transplant dAXP, erythrocyte deoxyadenosine nucleotides Ig, immunoglobulin
Accepted Jun 13, 2005.
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