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Biomedical subjects

M Magallón

Publications and source records attributed to M Magallón.

30 records · Page 2Linked to original sources

[Unusual bone tumor in a hemophiliac patient. Diagnosis using aspiration biopsy of the lesion].

Bone tumors due to repeated haemorrhages in haemophiliacs (haemophilic pseudotumours) usually are no diagnostic trouble. However, when x-ray findings are not conclusive, the differential diagnosis with malignant tumours may be difficult as bleeding complications hinder invasive diagnostic procedures. A fifteen year-old patient with severe haemophilia A is presented, who had a tumor in his left fibula with no previous traumatism. X-ray and CT scan images showed a broken cortical substance with reactive sclerosis and no alteration of the soft tissues. In order to establish the diagnosis and choose the adequate surgical management, aspiration with thin needle was performed through the cortical hole, under visual control with CT scan. A benign lesion was found upon study of the aspirate. No haemorrhagic or infectious complications developed after tumor dissection and filling with heterologous lyophilized bone. The final diagnosis was "giant cell reparative granuloma", an uncommon lesion in the fibula not previously reported in haemophiliacs. It was concluded that aspiration, when appropriately applied, may be a useful diagnostic procedure which should be borne in mind for the diagnosis of bone tumors in haemophiliacs.

Adolescent↗

[Pathogenesis of peripheral cytopenias in hemophiliac patients].

The frequent occurrence of peripheral cytopenias is a common clinical fact in patients with HIV-1 infection, and its pathogenetic mechanism is not clear, although several hypotheses have been proposed. Such cytopenias are frequently observed in haemophilic patients, in whom the immunologic alteration induced by continuous antigenic stimulants derived from plasma concentrate therapy has been postulated as an additional causative factor. One-hundred and forty five haemophiliacs treated with commercial antihaemophilic concentrates were studied. The patients were divided into three therapeutic groups according to the mean number of units of therapeutic factor VIII administered per Kg every year in the four years prior to the study (group I: less than 500 U; group II: between 501 and 1500 U; group III: more than 1500 U). The occurrence of cytopenias in the patients was co-ordinated with the presence or absence of HIV infection and the therapeutic group. The statistical studies showed clear correlation between peripheral cytopenias and presence of anti-HIV markers, regardless of the amount of concentrates perceived (except for the total neutrophil count).

Factor IX↗

[Neurologic and neuropsychologic manifestations in asymptomatic HIV positive subjects. Results of the first year follow-up].

Neurologic alterations were noted as important early from the description of the AIDS epidemic. At present, there is evidence that the Human Immunodeficiency Virus can be the aetiologic agent of the AIDS dementia complex. The natural history of this disease is not well known. Various longitudinal studies have been undertaken to assess the appearance of neurologic and neuropsychologic alterations in seropositive patients. Until now the results show that asymptomatic seropositive patients have not significant alterations. We are studying seropositive asymptomatic patients with haemophilia. The results of the first year of the study indicate that these patients, taken all together, have not significant alterations. However, neuropsychologic and subtle neurologic alterations were found in 3 patients (21%). If these findings are also observed in other similar studies, these group II "asymptomatic" patients will must be reclassified, with probable changes in management and prognosis.

Follow-Up Studies↗