[Celiac disease in children].
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Biomedical subjects
Publications and source records attributed to J Henker.
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A report is given on frequency investigations in the plasmocytoma in a dissection material of 36,985 cases of the years 1951 to 1971. 107 observations of multiple, nearly exclusively osseous plasmocytomas are evaluated concerning frequency of age and sex, affection of the skeleton as well as correlations between the degree of the histological maturity of the tumour cells and the produced para-proteins as well as the existence of the Bence-Jones-protein. The findings were compared with those of the literature.
About 8-years old boy with a brief clinical history and postmortem findings of a subactue encephalomyelopathy (Leigh-Syndrom) is reported. Pathohistological features were found to be of microcyst formation, vascular proliferation, proliferation of astrocytes, fibrillary gliosis, partial destruction of the myelin sheaths, relative preservation of the cell bodies of neurons. The lesions were symmetrical and involved the tegmentum mesencephali, the lamine quadrigemina, the substantia nigra, the tegmentum pontis, the tegmentum of the medulla oblongata, the basal protion of nucl. lentiformis, the ansa lenticularis, the thalamus, the hypothalamus and the gray matter of the spinal cord. Moderate changes were in the cerebellum. There was no marked histological changes in the cerebral cortex and white matter of the cerebrum, the mammillary bodies, the nervi and tracti optici and the peripheral nerves.
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A monozygous pair of twins with discordant presentation of coeliac disease is reported. The gluten-sensitive enteropathy in one of the twins might have been initiated by a virus infection.