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1.
Am J Clin Pathol ; 78(2): 141-9, 1982 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-6179423

RESUMEN

Acid phosphatase and alpha-naphthyl acetate esterase reaction patterns were evaluated in lymphocytes from patients with a variety of neoplastic and non-neoplastic conditions: leukemia, 59; NHL, 53; and reactive follicular hyperplasia, 23. Fifteen individuals with normal peripheral blood were also studied. For both enzymes, statistical analysis showed a strong correlation between a globular reaction pattern and T lymphocytic origin in both non-neoplastic lymph nodes and normal peripheral blood specimens (P less than 0.0001). A similarly strong correlation was found between a granular acid phosphatase pattern and T lymphocytic origin in cell isolated from non-neoplastic lymph nodes (P less than 0.0001) but not in those obtained from normal peripheral blood where this pattern was observed with equal frequency in B, T, and "null" lymphocytes (P = 0.415). A granular alpha-naphthyl acetate esterase pattern was correlated with non-T lymphocytes from normal peripheral blood (P less than 0.0001), but was observed with equal frequency in B, T, and "null" lymphocytes fron non-neoplastic lymph nodes (P = 0.76). In the eight T cell neoplasias studied, a globular pattern was evident in the majority of cells for both enzymes. In the majority of the B cell neoplasias, however, a granular pattern was observed for both enzymes.


Asunto(s)
Fosfatasa Ácida/sangre , Hidrolasas de Éster Carboxílico/sangre , Leucemia/enzimología , Linfocitos/enzimología , Linfoma/enzimología , Naftol AS D Esterasa/sangre , Histocitoquímica , Humanos , Hiperplasia/enzimología , Ganglios Linfáticos/patología , Formación de Roseta , Coloración y Etiquetado , Linfocitos T/enzimología
3.
Cancer ; 52(2): 318-21, 1983 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-6861074

RESUMEN

The clinical course of 41 previously reported patients with angioimmunoblastic lymphadenopathy with dysproteinemia (AILD) on whom follow-up information has been obtained for five or more years is described. Of the 41 patients, 27 achieved a complete remission (CR). The durations of the CR ranged from two to 214 months, with a median of 48 months. Nine of these 27 complete responders are still alive and well without evidence of disease, whereas the remaining 18 patients have died of pneumonia, septicemia, immunoblastic lymphoma, or unrelated causes. These 27 patients had a significantly longer median survival (51 mos) than did the 14 patients who had partial or no response (9 mos) (P = 0.0006). Only two of these 14 patients who did not initially achieve a CR are alive (survivals, 66 months and 70 months). There was a trend suggesting that patients who received combination chemotherapy which included prednisone had a slightly longer survival than did the remaining patients (P = 0.087). Lymphocytopenia was evident in a higher proportion of dead patients than in those who remained alive (P = 0.089).


Asunto(s)
Linfadenopatía Inmunoblástica/patología , Estudios de Seguimiento , Humanos , Pronóstico , Factores de Tiempo
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