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Biomedical subjects

M Wyss

Publications and source records attributed to M Wyss.

At least 109 records · Page 6Linked to original sources
PubMed1978

[Acute "high risk" and "low risk" juvenile lymphatic leukemia (proceedings)].

After an initial blood and thorax examination, 97 children with ALL were divided into "high risk" and "low risk" groups. From the 20 new "high risk" patients seen between 1972 and 1975 about one quarter were still alive 3 years later, the corresponding proportion from 37 "low risk" patients being about two thirds. Despite increased therapy, the number of early relapses does not appear to have decreased in the new "high risk" cases seen between 1976/77. An investigation of cell surface markers established that T-ALL always occurred in the "high risk" group, whereas B-negative/T-negative ALL was found not only in the "low risk" group but also occasionally in the "high risk" group.

B-Lymphocytes↗
PubMed1978

The applicability of the gland/wall ratio (Reid-Index) to clinicopathological correlation studies.

We studied at necropsy the bronchi of 49 subjects whose lung function has been measured during life. In each case the glands were examined in three bronchi by measuring the gland/wall ratio (Reid-Index) and by point-counting. The results of the two methods were compared: the data of the gland/wall ratio were normally distributed while those of the volume density established by point-counting were not. Gland/wall ratio and volume density of glands correlated moderately (RSp = 0.524). The function between them was not linear, in contrast with that between gland/wall ratio and gland thickness. The stereological background of these functions is discussed. In 34 subjects without restrictive lung disease FEV1 correlated inversely with the volume density of glands (RSp = -0.396), but not with the gland/wall ratio (Reid-Index)(RSp = -0.243). This discrepancy probably results from the different distribution of the data obtained by the two methods and from the non-linear function between them. These findings indicate that the gland/wall ratio (Reid-Index) is less applicable to clinicopathological correlations than the volume density of glands established by point-counting.

Adult↗
PubMed1978

[Congenital malabsorption of vitamin B12 (Imerslund's syndrome) in a premature girl with Down's syndrome (author's transl)].

A baby girl, born prematurely and with Down's syndrome, is hospitalized at the age of 51 days for a megaloblastic anemia. The anemia was caused by a selective malabsorption of vitamin B12 (Imerslund's syndrome), even in presence of intrinsic factor. The pathogenesis of different causes of vitamin B12 deficiency is discussed and the favourable development of this case after four years of treatment is shown.

Anemia, Macrocytic↗
PubMed1978

Multiple transfusions of HLA compatible blood in thalassaemia major.

The effect of polytransfusion regimen is studied in two patients with thalassaemia major over a period of 74 and 56 months respectively. In both cases we have observed an improvement of the general condition in the growth as well as a reduction of hepatosplenomegaly and cardiomegaly. Furthermore a decrease of reticulocytes, erythroblasts and fetal hemoglobin values was obtained. The consequences of these frequent transfusions on iron storage metabolism are discussed. The advantage of giving HLA compatible blood is demonstrated by only a weal alloimmunization in one patient having received 77 HLA compatible transfusions and the lack of immunization in the second patient after 52 transfusions. In 6 other patients affected with thalassaemia major and 3 more with bone marrow aplasia, transfusion with incompatible HLA blood was followed by immunization of variable importance.

Blood Transfusion↗
PubMed1978

[A case of endothelial splenic cyst in an infant].

The authors report a case of isolated splenomegaly in a healthy 7-year-old boy, not showing any other clinical or biological anomaly. The radiological examination (selective arteriography of left renal artery) and spleenscan were compatible with an intrasplenic process. The splenectomy was performed. The spleen was large (15/20 cm) and demonstrating a cystic lesion in the inferior pole. Histological examination revealed polycystic formations covered with endothelial type cells and associated with angiomatous multifocal lesions. Differential diagnosis of cystic lesions of the spleen is discussed and complete preoperative investigation is stressed.

Child↗
PubMed1977

Effects of parathyroid hormone on total protein, calcium magnesium, phosphorus, sodium and potassium concentrations of normal human parotid saliva.

The effects of parathyroid hormone (PTH) administered to six young normal adult subjects on protein, calcium, magnesium, phosphorus, sodium and potassium concentrations in parotid saliva have been studied in relation to the salivary flow rate. Stensen's duct was cannulated and excretion patterns of the constituents determined before and after stimulation of saliva production by lemon juice. After a control period (period 1), 50 U of PTH were given i.v. followed by an infusion of 2 U/min for 60-90 min (period 2). In the absence of any detectable changes in plasma, PTH induced a significant rise of salivary protein, calcium, and phosphorus concentrations at rest and following lemon juice stimulation, and of sodium concentration, but only at high flow rates for the latter. PTH did not change magnesium and potassium excretions significantly. Control experiments without PTH were performed on five other subjects. Protein, phosphorus and potassium concentrations did not change significantly between period 1 and period 2. Calcium and sodium excretions were reduced and magnesium excretion increased during period 2. These results provide evidence that PTH acts on the parotid gland by affecting protein secretion and electrolyte transport. Possible mechanisms of these changes are discussed.

Adult↗
PubMed1976

[Granulocyte transfusions. Technical data, granulocyte function and results].

A new method called "repetitive filtration leukopheresis" is described for granulocyte transfusion therapy. 23 patients received a total of 91 transfusions. All patients presented neutropenia of less than 300/mm3 and various kinds of infection resistant to antibiotic therapy. A favorable result was observed in 18 cases following these transfusions, which did not produce the secondary effects noted by others (chills, rash, fever, dyspnea). It was felt that this remarkable tolerance was a result of the collection procedure (elution at pH 7.4 ommission of centrifugation, thus securing the functional integrity of the cells). This impression was confirmed by the results of a battery of tests performed on the collected granulocytes, which included evaluation of their phagocytic and bacteriolytic functions and of their ability to break down a phagocytized antigen, together with measurements of lysosomial enzymes released in the supernatant.

Bacteriolysis↗
PubMed1976

Autologous marrow reconstitutions in severe aplastic anaemia after ALG pretreatment and HL-A semi-incompatible bone marrow cell transfusion.

Three consecutive patients considered to have end-stage acquired aplastic anaemia were given 100-160 mg/kg antilymphocyte globulin (ALG) i.v. followed by an infusion of 2-3.8 x 10(8) nucleated marrow cells/kg i.v. from HL-A one haplotype-identical, MLC-positive family donors. All patients showed autologous marrow reconstitutions lasting now 2-3 1/2 years. No clear-cut evidence of marrow engraftment could be established and no graft-versus-host disease was seen. It is assumed that these patients had some normal pluripotent haemopoetic stem cells which proved to be able of endoreduplication and of going into cycle after ALG conditioning and allogeneic marrow transfusion.

Adult↗
PubMed1975

[Post-transfusion HL-A alloimmunization in acute leukemia].

Patients with acute leukemia (AML and ALL) who received multiple transfusions of whole blood, platelets or granulocytes, may develop anti-HL-A immunization in spite of chemotherapy. The frequency of HL-A alloimmunization was studied in 21 patients with AML and in 11 children with ALL. Multispecific HL-A antibodies were detected in 10 patients with AML and in 8 with ALL. The presence of these antibodies was associated with febrile transfusion reactions and with immediate destruction of platelets or granulocytes. Selection of HL-A compatible donors eliminated those reactions and the platelet counts could be maintained at levels sufficient to avoid the risk of hemorrhage. It seems therefore warranted to transfuse exclusively HL-A compatible platelets or leukocytes, as soon as anti-HL-A immunization has been detected.

Antibody Formation↗