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The Broad Clinical Spectrum and Transplant Results of PNP Deficiency
Yael Dinur Schejter1, Ehud Even-Or2, Bella Shadur2,3,4
1Bone Marrow Transplantation Department, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. yaelsch@hadassah.org.il.
Purpose:
Purine nucleoside phosphorylase (PNP) is a known yet rare cause of combined immunodeficiency with a heterogeneous clinical presentation. We aim to add to the expanding clinical spectrum of disease, and to summarize the available data on bone marrow transplant for this condition.
Methods:
Data was collected from patient files retrospectively. A review of the literature of hematopoietic stem cell transplantation (HSCT) for PNP deficiency was conducted.
Results:
Four patients were treated in two centers in Israel. One patient died of EBV-related lymphoma with CNS involvement prior to transplant. The other three patients underwent successful HSCT with good immune reconstitution post-transplant (follow-up 8-108 months) and excellent neurological outcomes.
Conclusion:
PNP is a variable immunodeficiency and should be considered in various clinical contexts, with or without neurological manifestations. HSCT offers a good treatment option, with excellent clinical outcomes, when preformed in a timely manner.
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