Department of Pediatrics, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Eur J Pediatr. 2013 Jun;172(6):829-32. doi: 10.1007/s00431-013-2030-7. Epub 2013 May 16.
Secondary polycythemia with increased production of erythropoietin (EPO) is known to occur in kidney diseases such as hydronephrosis and cystic disease, but the mechanism remains unclear. We report an 18-year-old female with isolated renal relapse of acute lymphoblastic leukemia accompanied by polycythemia. At the relapse, she presented with bilateral nephromegaly, mild renal dysfunction, and erythrocytosis with increased serum EPO levels up to 52.1 mIU/mL (9.1-32.8). Renal biopsy demonstrated diffuse lymphoblastic infiltration. The expression of hypoxia-inducible factor (HIF)-1α, which is undetectable in normal kidney, was observed in the renal tubule epithelium compressed by lymphoblastic cells. These findings suggest that erythrocytosis was caused by renal ischemia due to leukemic infiltration. Polycythemia probably became apparent because of the lack of leukemic involvement of the bone marrow. With chemotherapy, the serum EPO level rapidly decreased to normal range accompanied by the normalization of kidney size and function. Renal leukemic infiltration may enhance EPO production, although not recognized in the majority of cases because of bone marrow involvement.
Our case has clarified the mechanism of previously reported polycythemia associated with renal diseases as renal ischemia. Furthermore, we have added renal ischemia resulting from tumor infiltration to the list of causes of secondary polycythemia.
继发于促红细胞生成素(EPO)产生增加的红细胞增多症已知发生于肾脏疾病如肾积水和囊性疾病,但机制尚不清楚。我们报告一例 18 岁女性,患有孤立性肾脏复发的急性淋巴细胞白血病并伴有红细胞增多症。在复发时,她表现为双侧肾肿大、轻度肾功能不全和红细胞增多症,血清 EPO 水平升高至 52.1 mIU/mL(9.1-32.8)。肾活检显示弥漫性淋巴母细胞浸润。缺氧诱导因子(HIF)-1α的表达在正常肾脏中不可检测,但在被淋巴母细胞压迫的肾小管上皮中观察到。这些发现表明红细胞增多症是由白血病浸润引起的肾缺血引起的。红细胞增多症可能变得明显是因为骨髓没有白血病浸润。随着化疗,血清 EPO 水平迅速降至正常范围,同时肾脏大小和功能也恢复正常。肾白血病浸润可能会增强 EPO 的产生,尽管由于骨髓受累,大多数情况下并未被识别。
我们的病例阐明了先前报道的与肾脏疾病相关的红细胞增多症的机制为肾缺血。此外,我们将肿瘤浸润引起的肾缺血添加到继发性红细胞增多症的原因列表中。