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肝泡状棘球蚴病患者肝自发性破裂:1 例报告。

Spontaneous liver rupture in a patient with peliosis hepatis: a case report.

机构信息

Department of Surgery, Inha University School of Medicine, Incheon 400-711, South Korea.

出版信息

World J Gastroenterol. 2009 Nov 21;15(43):5493-7. doi: 10.3748/wjg.15.5493.

Abstract

Peliosis hepatis is a rare pathological entity and may cause fatal hepatic hemorrhage and liver failure. Here, we present a young male patient with aplastic anemia, who had received long-term treatment with oxymetholone. The patient suffered from sudden onset of intra-abdominal hemorrhage with profuse hemoperitoneum. The patient was treated successfully with a right hemihepatectomy and is in good health after 13 postoperative months. We suggest that peliosis hepatis be considered in patients with hepatic parenchymal hematoma, especially in patients under prolonged synthetic anabolic steroid medication. The possibility of a potentially life-threatening complication of massive intra-abdominal bleeding should also be considered.

摘要

肝小泡状变是一种罕见的病理实体,可能导致致命性肝出血和肝功能衰竭。在这里,我们介绍一位接受长期氧甲氢龙治疗的再生障碍性贫血年轻男性患者。该患者突发腹腔内出血,大量血腹。患者成功接受了右半肝切除术,术后 13 个月健康状况良好。我们建议,对于肝实质血肿患者,尤其是长期使用合成合成代谢类固醇药物的患者,应考虑肝小泡状变。还应考虑可能发生危及生命的大量腹腔内出血的并发症。

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本文引用的文献

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Peliosis hepatis.肝紫癜病
Am J Pathol. 1950 Jan;26(1):1-15, incl 2 pl.
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