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Details of blood changes in 32 patients with pancytopenia associated with long-term exposure to benzene
  1. Muzaffer Aksoy,
  2. Koray Dinçol,
  3. Şakir Erdem,
  4. Turan Akgün,
  5. Günçaǧ Dinçol
  1. 2nd Internal Clinic of Istanbul Medical School, Capa, Istanbul, Turkey

    Abstract

    Aksoy, M., Dinçol, K., Erdem, Ş., Akgün, T., and Dinçol, G. (1972).Brit. J. industr. Med.,29, 56-64. Details of blood changes in 32 patients with pancytopenia associated with long-term exposure to benzene. A study was performed on 32 pancytopenic patients who had had long-term exposure to benzene. They had been subjected to high concentrations of benzene varying from 150 to 650 p.p.m. for from 4 months to 15 years. Apart from four, in whom the platelet count was normal, all had pancytopenia. As the bone marrow punctures of the pancytopenic patients showed a great variation from acellularity to hypercellularity, the patients were classified and studied according to the bone marrow findings.

    Anaemia was macrocytic in 14, in three of whom a megaloblastic erythropoiesis was detected. The findings in some patients, such as mild reticulocytosis, hyperbilirubinaemia, erythroblastaemia, an increase in quantitative osmotic fragility and in faecal urobilinogen excretion as well as elevated serum LDH levels, suggested that these might be attributed to either increased haemolysis or the presence of ineffective erythropoiesis.

    The HbF content in 20 out of 24 pancytopenic patients was above normal, ranging between 3·2% and 19·5%, with a mean of 6·1%. Mean values of HbF in groups with a hypoplastic, hyperplastic, and normoplastic bone marrow were essentially the same. The absolute amounts of HbF exceeded 400 mg/100 ml in only 8 out of 24 patients, all of whom survived.

    The HbA2 level was within normal limits in 21 out of 24 pancytopenic patients. It was definitely decreased in one and slightly so in three. These findings may suggest that HbA2 occasionally shows a tendency to decrease in some patients with chronic benzene poisoning. The maturation arrest in both the myeloid and erythroid elements was the most frequently encountered finding.

    In the bone marrow examinations, gaint erythroid precursors varying from 9% to 72% were detected in two patients. In one of them, who also had hepatosplenomegaly, the development of preleukaemia was accepted. Varying mortality rates were estimated in the above-mentioned groups. The results obtained from treatment with steroids, androgens, phyto-haemagglutinin, and oxymetholone are also described.

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