Chandra R S, Kapur S P, Kelleher J, Luban N, Patterson K
Arch Pathol Lab Med. 1984 Feb;108(2):168-71.
Hepatic tumors unassociated with cirrhosis were encountered in seven patients aged 10 to 19 years. Four patients had received androgens for aplastic anemia. Two patients had transfusional hemosiderosis. One patient had had a renal transplant 2 1/2 years ago. Two patients are alive at 2 3/4 and 2 1/2 years after surgical resections. Nodules were found at autopsy in the others. The tumors were well differentiated and, in the androgen-related cases, differed from the others in the following features: canalicular bile retention, mild nuclear atypia, and acinar formation. No mitoses, vascular invasion, or metastatic tumor were evident. The clinical setting was variable; different factors, including iron overload and androgen therapy, played a role in the development of tumor. Although the androgen-related cases showed mild cellular atypia, biologic evidence of malignancy was lacking as in most previous reports.
7例10至19岁的患者出现了与肝硬化无关的肝脏肿瘤。4例患者因再生障碍性贫血接受了雄激素治疗。2例患者有输血性含铁血黄素沉着症。1例患者在2年半前接受了肾移植。2例患者在手术切除后2年3/4和2年半时仍存活。其他患者在尸检时发现有结节。肿瘤分化良好,在雄激素相关病例中,在以下特征方面与其他病例不同:胆小管胆汁潴留、轻度核异型性和腺泡形成。未见有丝分裂、血管侵犯或转移瘤。临床情况各不相同;包括铁过载和雄激素治疗在内的不同因素在肿瘤的发生中起了作用。尽管雄激素相关病例显示出轻度细胞异型性,但与大多数先前报告一样,缺乏恶性肿瘤的生物学证据。