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Biomedical subjects

J Julien

Publications and source records attributed to J Julien.

214 records · Page 12Linked to original sources

Cardiac complications in non-insulin-dependent diabetes mellitus.

There is clear evidence of the negative influence of type I or II diabetes non-insulin-dependent diabetes mellitus (NIDDM) on the prevalence, severity, and prognosis of cardiovascular disease. Epidemiologic studies have confirmed the relationship between NIDDM and the occurrence of coronary artery disease (CAD) and cardiac heart failure (CHF). The clinical aspects of NIDDM cardiac complications include a high rate of silent events, which merit an improvement in their diagnosis and treatment. Besides pharmacological therapy, aggressive approaches including percutaneous transluminal coronary angioplasty (PTCA), and coronary surgery should be considered for the treatment of stable angina. IN some subgroups, the benefit of surgery has been proven. Available data indicate that diabetes (both type I and II) is a risk factor for an increase in morbidity and mortality following coronary bypass surgery. These data do not differentiate results between type I and type II diabetes. The indications for surgical revascularization are: three-vessel disease, left main artery stenosis, two-vessel disease including proximal left anterior descending artery stenosis, and two-vessel disease with left ventricular dysfunction. For PTCA, diabetes (type I more than type II) renders the technique more difficult and restenosis more frequent. From the results obtained in the general population and from a few specific studies, it is suspected that, in type II diabetes, PTCA and CABG are superior to conventional medical treatment. However, further specific studies on the beneficial effects of PTCA/CABG over optimal medical therapy are needed, at least in some angiographic conditions. Management of the diabetic patient with acute myocardial infarction is for the most part similar to the nondiabetic patient, with certain special considerations. Treatment includes thrombolytic therapy, invasive management, surgery, PTCA, beta blocker use, and aspirin use. Finally, diabetes mellitus is a cause of systolic and diastolic function, leading to clinical signs of CHF. Conventional medical therapy also applies to cardiac failure complicating diabetes. Medical therapy includes as the first line diuretics and angiotensin-converting enzyme inhibitors. We conclude that cardiac care can be improved in diabetic patients. For the time being, the first step is to improve the detection of coronary artery disease. As serious events are more likely to occur in the diabetic population, it would be easier (shorter studies and less patients) to demonstrate the benefit of a selected therapy. Further studies are therefore required. In the meantime, special efforts can be made: (1) prevent the development of coronary artery disease. Preventive measures aimed at the control of risk factors at the individual level must be optimal. What should be promoted is a more global approach to the patient, taking into account all parts of the risk factor profile, in order to amplify the reduction in risk and in cardiovascular morbidity and mortality. (2) When CAD is confirmed: the goal is to prevent all major cardiac events: unstable angina, myocardial infarction, sudden death, and CHF secondary to silent ischemic events. This can be achieved through the improvement of the accuracy of noninvasive diagnostic procedures, taking into account the cost of these procedures and the absence of pain perception in diabetic patients.

Angina Pectoris↗

Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 cases.

The authors recently reexamined the peripheral nerve biopsies from 42 patients with chronic inflammatory demyelinating polyneuropathy (CIDP). There were 27 males and 15 females, aged from 9 to 84 years, and 13 had relapses. No patient had vasculitis, monoclonal gammopathy, tumor, diabetes mellitus, Lyme disease, familial neuropathy, HIV, or any other immune deficiency. In the endoneurium, perivascular inflammatory cell infiltrates were present in only one case, but scattered histiocytes marked by KP1 on paraffin-embedded fragments were present in every case and there were no T-lymphocytes. At ultrastructural examination macrophage-associated demyelination was observed in 17 cases, of which 6 had relapses separated by intervals of several months or years. Axonal lesions without associated primary demyelination were observed in 4 cases and 3 of these had relapses. Thirty-two patients had mixed lesions of demyelination and axonal involvement. This study confirms other recent data indicating that in all cases of CIDP, macrophages are present in the endoneurium. Macrophage-associated demyelination is the characteristic feature of demyelinating forms. On the other hand, isolated primary axonal forms, which have been known since 1989, are relatively frequent and prone to relapses.

Adolescent↗

Myelin modifications in 8 cases of peripheral neuropathy with Waldenström's macroglobulinemia and anti-MAG activity.

Characteristic myelin modifications in patients with IgM monoclonal gammopathy and anti-MAG activity have mainly been studied in cases of undetermined significance, but also exist in cases with indolent Waldenström's macroglobulinemia, i.e., when lymphoplasmocytic infiltration in bone marrow is 15% or more, without any visceral involvement. Since 1983, the authors have examined nerve biopsies from 8 cases with Waldenström's macroglobulinelia by direct immunofluorescence examination on frozen sections and ultrastructural examination. At direct immunofluorescence, fixation of anti-IgM serum on myelinated fibers was present in 7 cases. At ultrastructural examination, a widening of some myelin lamellae at the periphery of a few fibers was visible in 8 cases. A few fibers with hypermyelination were present in 5 cases. In 2 of these 5 cases widening of some myelin lamellae was present in numerous fibers, 88% in one of them. Frequently, there was a major widening of some myelin lamellae with dilated lamellae present in the inner part of the myelin sheath. Certain lamellae were more dilated, up to 50 nm. Occasionally, enlarged lamellae were not compacted with each other. The authors also examined nerve biopsies from 36 patients with IgM monoclonal gammopathy of undetermined significance and anti-MAG activity, but found only one case with major widening of some myelin lamellae. Five other cases with major widening of some myelin lamellae, 4 Waldenström's macroglobulinemia and 1 IgM monoclonal gammopathy of undetermined significance, have been reported. Given that demyelinating neuropathies are far more numerous in cases with IgM monoclonal gammopathy of undetermined significance, it is likely that cases of indolent Waldenström's macroglobulinemia are prone to develop major myelin modifications, possibly due to another mechanism, added to the classic anti-MAG activity.

Aged↗

Subacute inflammatory polyneuropathy: two cases with plasmacytoid histiocytes in the endoneurium.

Inflammatory polyneuropathies are mainly known by their acute form, Guillain-Barré syndrome, but there are also chronic cases and all are considered as having an autoimmune mechanism. In each form, peripheral nerve biopsies show scattered macrophages in the endoneurium and in certain cases macrophages invade the Schwann cell cytoplasm and destroy the myelin sheath. In rarer cases there is a primary axonal degeneration. The authors studied two chronic cases, which both exhibited mixed primitive axonal and demyelinating lesions, with peculiar histiocytes in the endoneurium. These rounded cells were characteristically well marked by KP1 but showed well-developed rough endoplasmic reticulum cysternae at ultrastructural examination. Such plasmacytoid histiocytes have mainly been studied in subacute lymphadenopathies and have been only briefly illustrated in a few cases of peripheral neuropathies due to Lyme disease or HIV infection. The two cases reported here had no associated diseases and probably correspond to a peculiar subacute autoimmune reaction.

Adult↗

[Drachman's "ophthalmoplegia plus" or Kearns and Shy syndrome. Apropos of 2 cases with mitochondrial abnormality ultrastructurally demonstrated in the muscle].

Two typical cases of the Kearns and Shy syndrome are reported. Some of the authors have previously published observations on simple ocular myopathy and oculo-pharyngeal dystrophy associated with abnormalities of the mitochrondria in skeletal muscle cells. This disease, which is still called "ophthalmoplegia plus", combines a progressive external ophthalmoplegia, muscular defects and varied neurological signs with other symptoms particularly retinal, endocrine and cardiac. Histo-enzymological and ultra-structural studied of a fragment of skeletal muscle confirm the presence of mitochondrial anomalies.

Adult↗

[Peripheral neuropathies i- Waldenstrom's disease. Histological and ultrastructural studies of 5 cases].

In four cases it was the existence of peripheral neuropathy which led to the discovery of macroglobulinemia within an interval from 1 to 11 years. The treatment of the disease also markedly improved the peripheral neuropathy in three cases. Two patients died. Two of the biopsies of the peripheral nerve showed infiltration by atypical lymphocytes. Ultrastructural changes in the five cases were variable. Marked axonal involvement in the two cases with cellular infiltration. In one of these two cases it was combined with segmental demyelinization. This lesion was clearly predominant in the three other cases. In one of them demyelinization occurred in a very peculiar way with dilation of the internal part of the mesaxone going on in the most peripheral layers of the myelin. Discussion of the mechanisms of the involvement of the peripheral nervous parenchyma in Waldenström's disease. Cellular infiltrations, amorphous deposits, changes in the capillaries and macroglobuline may occur.

Adult↗

[Arterial hypertension in heart transplant recipients].

Arterial hypertension is frequent after cardiac transplantation. Since cyclosporin was introduced its incidence has risen up to 40 to 100 per cent of the patients. Its date of onset and severity are variable. Arterial hypertension acts on the heart by increasing left ventricular hypertrophy and transplant dysfunction and on the kidney by aggravating the cyclosporin-induced renal impairment which is often present. Several mechanisms have been suggested to account for the occurrence of hypertension in these patients, including poor neurological control of blood pressure, a hypothetical haemodynamic effect and the influence of corticosteroids and cyclosporin. Cyclosporin seems to play the main role. The treatment of this iatrogenic arterial hypertension remains to be precisely determined.

Adrenal Cortex Hormones↗

[Cerebral infarction and migrainous attack. Angiographic and CT scan studies (author's transl)].

A lateral homonymous hemianopia appareared in a 40 years old housewife during a migrainous attack and persisted as sequella. Angiographic study was normal and CT scan showed an area of low density at the right occipital level enhancing with heterogenous aspect after the iodinate injection. The occurrence of a cerebral infarction during a migrainous attack is probably due to numerous factors.

Adult↗

[Trigeminal sensory neuropathy and Sharp's syndrome (author's transl)].

Neurological manifestations are rarely observed with mixed connective tissue disease (MCTD). The most frequent is a trigeminal sensory neuropathy which sometimes appeared as an early symptom. We report a new case of bilateral isolated trigeminal sensory neuropathy during M.C.T.D. Similitudes can be drawn with trigeminal neuropathies observed in connective tissue diseases such as scléroderma. Mechanisms are discussed.

Female↗