L. Zappatini-Tommasi

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A case of Farber disease is reported and the ultrastructural pathology of the disease is reviewed. The present case showed the typical clinical picture of Farber disease. Acid ceramidase deficiency was demonstrated biochemically. Ultrastructural features of one subcutaneous nodule and a skin biopsy are described. Three lysosomal inclusions characterize(More)
A case of Farber disease is reported and the ultrastructural pathology of the disease is reviewed. The present case showed the typical clinical picture of Farber disease. Acid ceramidase deficiency was demonstrated biochemically. Ultrastructural features of one subcutaneous nodule and a skin biopsy are described. Three lysosomal inclusions characterize(More)
The hitherto conventional classification of primitive brain tumours has been recently, and somewhat tentatively, revised for pediatric pathology: a new class of tumours, named Primitive Neuroectodermal Tumours (PNET) has been established, encompassing many undifferentiated, small cell tumours of uncertain origin, mainly medulloblastomas. This paper deals(More)
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