一例青少年B淋巴细胞白血病伴复发性基因异常化疗后无症状性肠内肺病。

The Korean Journal of Hematology Pub Date : 2012-03-01 Epub Date: 2012-03-28 DOI:10.5045/kjh.2012.47.1.74
Dae-Kyu Shin, Jisu Oh, Harry Yoon, Jo Eun Kim, So Young Chong, Doyeun Oh
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引用次数: 9

摘要

肠肺病(PI)是一种罕见的疾病,其特征是肠粘膜下层或浆膜下有多个肺囊肿。在此,我们报告一例罕见的18岁男性B淋巴细胞白血病伴复发性遗传异常的化疗诱导后无症状PI。患者经保守治疗,恢复无并发症。在血液恶性肿瘤化疗期间或之后,PI的可能性应被认为是一种并发症。除非有并发症,如腹膜炎、肠穿孔和严重败血症,否则应考虑保守治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Asymptomatic pneumatosis intestinalis following chemotherapy for B lymphoblastic leukemia with recurrent genetic abnormalities in an adolescent patient.

Asymptomatic pneumatosis intestinalis following chemotherapy for B lymphoblastic leukemia with recurrent genetic abnormalities in an adolescent patient.

Asymptomatic pneumatosis intestinalis following chemotherapy for B lymphoblastic leukemia with recurrent genetic abnormalities in an adolescent patient.

Asymptomatic pneumatosis intestinalis following chemotherapy for B lymphoblastic leukemia with recurrent genetic abnormalities in an adolescent patient.

Pneumatosis intestinalis (PI) is a rare condition characterized by multiple pneumocysts in the submucosa or subserosa of the bowel. Here, we report a rare case of asymptomatic PI after chemotherapy induction in an 18-yr-old man with B lymphoblastic leukemia with recurrent genetic abnormalities. The patient was treated conservatively and recovered without complications. The possibility of PI should be considered as a complication during or after chemotherapy for hematologic malignancies. Conservative treatment should be considered unless there are complications, including peritonitis, bowel perforation, and severe sepsis.

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