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1.
Spinal Cord ; 41(10): 577-85, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14504618

ABSTRACT

STUDY DESIGN: Case report of recovering radiation myelopathy. OBJECTIVE: To present autopsy and functional imaging findings on a unique case of slowly recovering radiation myelopathy with the aim of the clarification of the underlying mechanism. PATIENT: The cervical spinal cord and the distal part of the medulla oblongata of a 36-year-old thyroid cancer patient had been incorrectly irradiated with a total dose of 61 Gy and a fraction size of 3.4 Gy (J Neurol Sci 1999; 163:39-43), resulting in incomplete cervical transection with a 5-month latency period following the termination of radiotherapy. This was followed by a 9.5-year spontaneous improvement until her demise, during which the check-ups were supplemented by positron emission tomography (PET) investigations; these indicated increased [18F]deoxyglucose and [15O]butanol uptakes, but a diminished [11C]methionine accumulation by the irradiated spinal cord segment. RESULTS: Autopsy revealed demyelination (with axonal loss) and neuronal damage in the cervical spinal cord and the distal part of the medulla oblongata. In the same region, only minimal vascular injury (thickening of some of the capillary walls) was detected, but not cell proliferation or chronic inflammation. Bilateral, secondary pyramidal tract degeneration caudal to the irradiated segment was observed. The PET and autopsy findings, although separated by 2 years, are consistent. CONCLUSIONS: The pathological state of the spinal cord revealed by the autopsy is concordant with the incomplete cervical transection, implying that the functional recovery is supported by a process that probably differs from the restoration of the mechanism destroyed by the radiotherapy. For the restoration of the function, we suggest an altered conduction mechanism of the action potential, involving an increased number of sodium channels along the demyelinated segments of the injured axons, which is fully congruent with the PET findings.


Subject(s)
Blood Vessels/radiation effects , Demyelinating Diseases/etiology , Radiotherapy/adverse effects , Spinal Cord Diseases/etiology , Spinal Cord Diseases/pathology , Adult , Autopsy , Cervical Vertebrae/diagnostic imaging , Cervical Vertebrae/radiation effects , Demyelinating Diseases/metabolism , Demyelinating Diseases/physiopathology , Fatal Outcome , Female , Fluorodeoxyglucose F18/pharmacokinetics , Humans , Medulla Oblongata/diagnostic imaging , Medulla Oblongata/pathology , Medulla Oblongata/radiation effects , Meningitis/complications , Methionine/pharmacokinetics , Nerve Degeneration/etiology , Nerve Degeneration/pathology , Neurons/pathology , Oxygen Radioisotopes/pharmacokinetics , Paraplegia/etiology , Radiation Injuries/complications , Radiography , Spinal Cord/diagnostic imaging , Spinal Cord/metabolism , Spinal Cord/pathology , Spinal Cord/radiation effects , Spinal Cord Diseases/diagnostic imaging , Spinal Cord Diseases/metabolism , Spinal Cord Diseases/physiopathology , Thyroid Neoplasms/radiotherapy , Tomography, Emission-Computed
3.
Hum Exp Toxicol ; 17(4): 206-11, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9617632

ABSTRACT

To indicate the immunotoxic potential of chemicals the examinations prescribed by OECD Guideline 407 were extended by the following additional toxicological, haematological, histopathological, and immune function examinations: absolute and relative organ weight of spleen, thymus, popliteal lymph nodes, lung and brain; histopathology of thymus, mesenteric lymph nodes, popliteal lymph nodes, bone marrow (femur), Peyer's patches (ileum), lungs and colon; PFC assay (spleen), T cell proliferation and NK cell assay. Two well known immunosuppressants Azathioprine (AZA) and Cyclosporine A (CysA) were chosen as model compounds at a dose range which do not cause visible toxic signs on the animals during a 28 days treatment period. The results show that the applied experimental system is much more sensitive in detection of the immunotoxic potential of these two compounds in a low dose range than the examination required by OECD Guideline 407 are.


Subject(s)
Cytotoxicity, Immunologic , Immunosuppressive Agents/toxicity , T-Lymphocytes/drug effects , Toxicity Tests , Administration, Oral , Animals , Azathioprine/administration & dosage , Azathioprine/toxicity , Blood Cell Count , Bone Marrow Cells/drug effects , Bone Marrow Cells/pathology , Cell Division/drug effects , Cyclosporine/administration & dosage , Cyclosporine/toxicity , Guidelines as Topic , Immunosuppressive Agents/administration & dosage , Killer Cells, Natural/drug effects , Lymphoid Tissue/drug effects , Lymphoid Tissue/pathology , Male , Organ Size/drug effects , Rats , Rats, Wistar
4.
Zentralbl Allg Pathol ; 135(6): 549-52, 1989.
Article in German | MEDLINE | ID: mdl-2683502

ABSTRACT

An account is given of possibilities and mechanisms of regression of arteriosclerosis. Reference is made to animal experiments and to angiographic investigations of man, and the assumption is derived that even in man arteriosclerosis is to a certain extent capable of regression. This view applies preferentially to lipidous alterations. A distinction is made between two mechanisms underlying regression. One of them is attributed to reduction of existing hypercholesterolaemia, while the other is related to regression via action of so far unknown wall factors, without lowering of blood cholesterol.


Subject(s)
Arteriosclerosis/therapy , Hypercholesterolemia/therapy , Humans
5.
Z Gesamte Inn Med ; 41(14): 391-3, 1986 Jul 15.
Article in German | MEDLINE | ID: mdl-3765739

ABSTRACT

Atherosclerosis is-even in advanced state--able to regression and this event may occur under certain circumstances. Regression can be of such size, as to lengthen significantly life of patient, relieving essentially his complaints. This regression may be increased by drugs and promoted with alteration of life-circumstances.


Subject(s)
Arteriosclerosis/pathology , Arteries/pathology , Arteriosclerosis/therapy , Humans , Prognosis , Thrombosis/pathology
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