Kim Seon Young, Kwon Joong Goo, Kim Myung Hwan, Oh Jae Young, Park Jin Hong, Park Kyung Chan, Ryoo Jung Il, Ryoo Hun Mo
Department of Internal Medicine, Catholic University of Daegu School of Medicine, Daegu, Korea.
Korean J Gastroenterol. 2012 Nov;60(5):320-4. doi: 10.4166/kjg.2012.60.5.320.
Protein-losing enteropathy (PLE) is a syndrome characterized by excessive gastrointestinal protein loss, resulting in hypoproteinemia and edema. A variety of benign and malignant conditions can be associated with PLE and acute leukemia is a very rare cause of PLE. We report a case of PLE associated with acute lymphoblastic leukemia. A 27-year-old man was admitted due to watery diarrhea, epigastric pain and bilateral leg edema. Laboratory findings showed hypoproteinemia and polycythemia. The diagnosis of PLE and acute lymphoblastic leukemia were confirmed on the measurement of fecal a1-antitrypsin clearance and bone marrow examination. After systemic chemotherapy and autologous stem cell transplantation, his clinical symptoms and abnormal laboratory findings were gradually improved.
蛋白丢失性肠病(PLE)是一种以胃肠道蛋白质过度丢失为特征的综合征,可导致低蛋白血症和水肿。多种良性和恶性疾病都可能与PLE相关,而急性白血病是PLE非常罕见的病因。我们报告一例与急性淋巴细胞白血病相关的PLE病例。一名27岁男性因水样腹泻、上腹部疼痛和双侧腿部水肿入院。实验室检查结果显示低蛋白血症和红细胞增多症。通过检测粪便α1-抗胰蛋白酶清除率和骨髓检查,确诊为PLE和急性淋巴细胞白血病。经过全身化疗和自体干细胞移植后,他的临床症状和实验室异常结果逐渐改善。