Niemann-Pick disease type C (a cellular cholesterol lipidosis) treated by bone marrow transplantation
Autor: | Dong-Tsamn Lin, Sheng-Chuan Huang, S. S. F. Peng, Kai-Hsin Lin, Wuh-Liang Hwu, Y.-S. Hsu, R.-L. Chen, Meng-Yao Lu |
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Rok vydání: | 1999 |
Předmět: |
Male
Pathology medicine.medical_specialty Transplantation Conditioning Hepatosplenomegaly Spleen Central nervous system disease Lysosomal storage disease Medicine Humans Busulfan Cyclophosphamide Bone Marrow Transplantation Niemann-Pick Diseases Transplantation Niemann–Pick disease type C Lung business.industry Infant Hematology medicine.disease medicine.anatomical_structure Child Preschool Female Bone marrow medicine.symptom business Niemann–Pick disease Immunosuppressive Agents |
Zdroj: | Bone marrow transplantation. 24(1) |
ISSN: | 0268-3369 |
Popis: | Bone marrow transplantation (BMT) has been used for a wide variety of lysosomal storage diseases with encouraging results. We report a 3-year 5-month-old girl with Niemann-Pick type C disease (NPC) who received an allogeneic BMT. The patient presented with repeated lower respiratory tract infections, hepatosplenomegaly, failure to thrive, and developmental delay. Chest computed tomography (CT) revealed diffuse interstitial lung infiltration. Bone marrow and liver biopsies revealed abundant lipid-filled foamy macrophages. Skin fibroblast sphingomyelinase assay revealed partial deficiency. The ability of her skin fibroblasts to esterify cholesterol was very low, and the cells stained brightly for free cholesterol. She received BMT from a healthy HLA-identical male sibling donor at the age of 2 year 6 months. Full engraftment was evidenced by repeated bone marrow sex chromosome studies. Regression of the hepatosplenomegaly, markedly reduced foamy macrophage infiltration in bone marrow, and decreased interstitial lung infiltration was noted 6 months after BMT. Her neurological status, however, deteriorated. Follow-up magnetic resonance image (MRI) revealed progressive, diffuse brain atrophy. We conclude that resolution occurred in the liver, spleen, bone marrow and lung following successful engraftment. Such a response is remarkable since the underlying problem involves a membrane receptor for cholesterol. This positive response might be due to replacement of the monocyte-phagocytic system or it may imply the existence of cross-correction in the NPC membrane receptor defect by BMT approach. Since BMT did not halt the neurological deterioration, it is unlikely to be an adequate treatment for NPC. |
Databáze: | OpenAIRE |
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