目前强化治疗儿童急性淋巴细胞白血病后的肝脏组织学:微泡性脂肪改变和铁沉着是主要发现。

Päivi Halonen, Jorma Mattila, Tarja Ruuska, Matti K Salo, Anne Mäkipernaa
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引用次数: 26

摘要

背景:在儿童急性淋巴细胞白血病(ALL)的现代强化治疗中,血清肝酶达到相当高的水平。由于没有治疗后肝脏组织病理学的最新数据,我们对该主题进行了研究。方法:对27例连续接受标准(SR)和中危(IR) ALL治疗的儿童进行肝活检标本评估、血清肝功能检查和血脂测定,年龄为3.5-17.6岁。结果:所有患者肝脏组织学均不完全正常。27例患者中有25例(93%)检测到脂肪浸润,27例患者中有19例(70%)检测到铁沉着。14人(52%)两者都有。3例(11%)患者除了脂肪改变和铁质沉着外,还伴有轻度门脉和/或门脉周围纤维化。脂肪变化以微泡性为主。大多数情况下,铁沉着是II/IV至III/IV级(占16/19或84%)。未发现肝炎或肝硬化。纤维化患者血清总胆固醇和ldl -胆固醇水平高于脂肪改变患者(P = 0.036, P = 0.042)或铁沉着+/-脂肪改变患者(P = 0.036, P = 0.042)。在连续的ALT测量中,纤维化组比脂肪改变组或铁苷沉积组更常达到300 U/L或更高的值(在Kruskall-Wallis试验中,分别有33对12或4%的测量值,P = 0.014)。结论:目前治疗儿童ALL后肝脏的主要表现为微泡性脂肪改变和铁质沉着。纤维化很少发生。连续血清谷丙转氨酶测量值高或血清脂质谱紊乱可能有助于决定是否需要肝活检。
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Liver histology after current intensified therapy for childhood acute lymphoblastic leukemia: microvesicular fatty change and siderosis are the main findings.

Background: During modern intensified therapy for childhood acute lymphoblastic leukemia (ALL) serum liver enzymes reach fairly high levels. Since no recent data on liver histopathology after therapy are available, we conducted a study of the subject.

Procedure: Liver biopsy specimens were evaluated and serum liver function tests and lipid profiles measured from 27 consecutive children, aged 3.5-17.6 years, treated according to the regimens for standard (SR) and intermediate risk (IR) ALL.

Results: None of the patients had entirely normal liver histology. Fatty infiltration was detected in 25 out of 27 (93%) and siderosis in 19 out of 27 patients (70%). Fourteen (52%) had both. Three (11%) also had mild portal and/or periportal fibrosis in addition to fatty change and siderosis. Fatty change was mainly microvesicular. Siderosis was in most cases grade II/IV to III/IV (in 16/19 or 84%). No hepatitis or cirrhosis was found. Serum total and LDL-cholesterol levels were higher in the patients with fibrosis than in the patients with fatty change (P = 0.036, P = 0.042) or with siderosis +/- fatty change (P = 0.036, P = 0.042). In serial ALT measurements a value of 300 U/L or more was oftener reached in the fibrosis than in the fatty change or siderosis groups (in 33 vs. in 12 or in 4% of the measurements, respectively, P = 0.014, in Kruskall-Wallis test).

Conclusions: Microvesicular fatty change and siderosis are the main liver findings after current therapy for childhood ALL. Fibrosis occurs rarely. High values in serial serum ALT measurements repeatedly or a disturbed serum lipid profile may facilitate decisions about the need for a liver biopsy.

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