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Biomedical subjects

R Scolozzi

Publications and source records attributed to R Scolozzi.

At least 37 records · Page 2Linked to original sources
PubMed1983

[Dysmyelopoietic syndrome 7 years after melphalan treatment of multiple myeloma. Clinical case].

A case of myelodysplasia (refractory anaemia with excessive blasts) arising 7 years after a 3 year period of intermittent monthly treatment cycles with melphalan for multiple myelomas is reported. This is another example of preleukaemic syndrome possibly caused by melphalan. Among the possible pathogenetic mechanisms, the incidence of cyclic episodes of medullary hypoplasia are emphasised.

Blood Transfusion↗
PubMed1983

[Prognostic factors and response to chemotherapy in breast cancer. bibliographic review].

The recent literature on prognostic factors in breast cancer was examined with regard to: early or delayed diagnosis, age, menopause, tumour site and size, histological type and grading, involvement of lymph nodes, clinical stage, local recurrence, and distant metastasis. With respect to prognostic factors connected with the response to therapy, the following points were considered: menopause, involvement of lymph nodes, dimensions, clinical stage, free interval, performance and loss of weight, particular sites of metastasis, radiotherapy, oestrogen receptors, prior endocrine management, and certain body fluid parameters (haemoglobin, total lymphocytes, platelets, and white cells, albumin, LDH, SGOT, alkaline phosphatase, blood bilirubin and calcium). Radiotherapy appears to make patients less responsive to subsequent antiblastic treatment, whereas premenopausal status, good psychological and physical efficiency, and prior endocrine management seem to play a positive role in the response to chemotherapy.

Adult↗
PubMed1981

[Prognosis of chronic lymphatic leukemia. Retrospective study of the survival period 47 patients].

Forty-seven consecutive patients with chronic lymphocytic leukemia (CLL) followed in the Clinica Medica and the Sezione di Ematologia of Ferrara from January 1966 to June 1979 were classified according to the staging system of Rai and to age, sex and the occurrence of enlarged spleen or liver or both. Analysis of actuarial survival curves revealed the following: 1) the method of staging proposed by Rai was confirmed to be a reliable predictor for prognosis of CLL; 2( neither age nor sex do appear to be prognostic factor; 3) the enlarged liver did not appear to make worse the prognosis of CLL, probably by hepatomegalies due to other aetiologies. Furthermore the bound of peripheral lymphocytosis of 15,000/mm3, also according to other authors, seems to be too high: numerous cases of undoubted CLL with smaller lymphocytosis ae left out of this and other statistics published on CLL.

Adult↗
PubMed1979

[Indirect immunoelectrophoresis in the study of urinary proteins].

The indirect immunoelectrophoresis applied to the proteinurias is a simple and quick method, of usual execution, that makes use of not concentrated urines and discriminant between physiological and pathological proteinurias. The results obtained from a various casistic, collected in many years are presented. For the correlation which exist between morphological isototype and immunoelectropherogram, sometimes, it is possible to go up to the diagnosis of nephropathy also without applying to the renal biopsy.

Albuminuria↗
PubMed1978

[The significance of cryoglobulins and cryohemagglutinins. Immunological and clinical study of 39 cases].

In about 5 years of clinical and immunological research, 39 cases of cryoplasmopathies (5 with cryoglobulinaemia and 34 with cryohaemoagglutinaemia) were identified on the basis of immunological typing studies (immunoelectrophoresis, immunodiffusion, identification and isolation of cryoantibodies, cryocrit, titration, identificcation of antibody specificity). Discussion and physiopathological interpretation of possibly associated cases and diseases are conducted on the basis of personal immunological data and the most recent literature on matters of clinical immunohaematology.

Agranulocytosis↗
PubMedDate not supplied

[Hyper-IgD syndrome and other hereditary periodic fever syndromes].

Hereditary periodic fever syndromes are a group of systemic disorders characterized by recurrent attacks of systemic inflammation (autoinflammation) without infectious or autoimmune cause. The hyper-IgD syndrome (HIDS) is a rare autosomal recessive inflammatory disorder characterized by recurrent fever, increased serum IgD (normal value < 100 U/ml) and generalized inflammation (lymphadenopathy, arthralgias/arthritis, abdominal complaints, skin rash, and headache). The attacks persist during the entire life although frequency and severity tend to diminish with age. HIDS is caused by specific mutations in the gene encoding mevalonate kinase, resulting in depressed enzymatic activity. At present the therapy for the syndrome is only supportive. Other than HIDS, other hereditary systemic inflammatory disorders have been described: the Familial Mediterranean Fever, the tumour necrosis factor receptor associated periodic syndrome (TRAPS), a disease related to the mutations of one of the TNF receptors, the Familial Cold Urticaria and the Muckle-Wells syndrome. The differential diagnosis with other causes of periodic fever is crucial for assessing appropriate management and treatment.

Chromosomes, Human↗