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急性淋巴细胞白血病中的环化学图谱。

Cycochemical profiles in acute lymphoblastic leukemia.

作者信息

McKenna R W, Brynes R K, Nesbit M E, Bloomfield C D, Kersey J H, Spanjers E, Brunning R D

出版信息

Am J Pediatr Hematol Oncol. 1979 Fall;1(3):263-75. doi: 10.1097/00043426-197923000-00011.

Abstract

Lymphoblasts from 61 untreated patients with acute lymphoblastic leukemia (ALL), classified according to the French-American-British (FAB) morphologic classification, were studied for cytochemical characteristics and membrane surface markers. Seventy-three % (eight of 11) of patients with E-rosette positive lymphoblasts (T ALL) had strong focal paranuclear acid phosphatase (AcP) activity in more than 75% of their lymphoblasts; lymphoblasts from only 6% (three of 48) (p = 0.005) of patients with E-rosette negative, surface immunoglobulin negative lymphoblasts (non-T, non-B ALL) exhibited this characteristic AcP activity. The non-T, non-B ALL cases that manifested focal paranuclear AcP activity had clinical features more characteristic of the T ALL cases. The distribution of beta-glucuronidase activity in the lymphoblast cytoplasm was similar to that of AcP for T ALL and non-T, non-B ALL but the stain was generally more difficult to interpret THan the AcP and was a less reliable indicator of immunologic type of ALL. The periodic acid-Schiff (PAS) and nonspecific esterase stains were not useful in distinguishing between T ALL and non-T, non-B ALL but PAS negativity was associated with certain clinical features within the non-T, non-B ALL group. Cytochemical evaluation of the lymphoblasts at diagnosis in patients with ALL may be useful in identifying subsets of ALL that have distinct immunologic and clinical characteristics and important therapeutic and prognostic implications.

摘要

对61例未经治疗的急性淋巴细胞白血病(ALL)患者的淋巴母细胞进行了研究,这些患者根据法美英(FAB)形态学分类进行分类,研究内容包括细胞化学特征和膜表面标志物。E花环阳性淋巴母细胞(T-ALL)患者中有73%(11例中的8例)其淋巴母细胞中超过75%具有强烈的局灶性核旁酸性磷酸酶(AcP)活性;E花环阴性、表面免疫球蛋白阴性的淋巴母细胞(非T、非B-ALL)患者中只有6%(48例中的3例)(p = 0.005)的淋巴母细胞表现出这种特征性的AcP活性。表现出局灶性核旁AcP活性的非T、非B-ALL病例具有更类似于T-ALL病例的临床特征。T-ALL和非T、非B-ALL的淋巴母细胞胞质中β-葡萄糖醛酸酶活性的分布与AcP相似,但该染色通常比AcP更难解释,并且是ALL免疫类型的较不可靠指标。过碘酸希夫(PAS)和非特异性酯酶染色在区分T-ALL和非T、非B-ALL方面没有用处,但PAS阴性与非T、非B-ALL组内的某些临床特征相关。对ALL患者诊断时的淋巴母细胞进行细胞化学评估可能有助于识别具有不同免疫和临床特征以及重要治疗和预后意义的ALL亚组。

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