Tamura Akihiro, Uemura Suguru, Saito Atsuro, Okubo Saki, Nino Nanako, Tahara Teppei, Yokoi Takehito, Kishimoto Kenji, Ishida Toshiaki, Hasegawa Daiichiro, Kawasaki Keiichiro, Yoshimoto Seiji, Nakao Hideto, Yoshida Makiko, Kosaka Yoshiyuki
Department of Hematology and Oncology, Children's Cancer Center, Hyogo Prefectural Kobe Children's Hospital, Minatojima-Minamimachi 1-6-7, Chuo-ku, Kobe, 650-0047, Japan.
Department of Neonatology, Hyogo Prefectural Kobe Children's Hospital, Minatojima-Minamimachi 1-6-7, Chuo-ku, Kobe, 650-0047, Japan.
Int J Hematol. 2017 Nov;106(5):711-717. doi: 10.1007/s12185-017-2248-7. Epub 2017 May 18.
Congenital pure erythroid leukemia is exceedingly rare and poses a diagnostic challenge. We report an atypical case of congenital pure erythroid leukemia that did not express typical erythroid markers. The patient presented with a high white blood cell count with blastic cells at birth. Although flow cytometric analyses of peripheral blood and bone marrow showed a large CD45-negative cell population, we did not identify any evidence of monoclonality. While the circulating blasts decreased with only supportive care, hepatomegaly with multiple nodules was accompanied by liver failure, disseminated intravascular coagulation, and development of hemophagocytic lymphohistiocytosis. Pathological examination of the liver biopsy specimen revealed a small round cell tumor that was negative for nearly all hematopoietic cell markers, including classical erythroid cell markers, and positive for CD43, CD71, and E-cadherin, an early erythroid marker epithelial calcium-dependent adhesion protein, suggesting that these tumor cells originated from an immature erythroblast. We found high β-catenin and c-Myc protein expression, which were not previously described in pure erythroid leukemia. Cytosine arabinoside temporarily alleviated clinical symptoms; however, the patient died of progressive disease at 8 months of age. This case indicates that E-cadherin is useful for diagnosing pure erythroid leukemia, even in immature cases.
先天性纯红细胞白血病极为罕见,且诊断具有挑战性。我们报告了一例非典型的先天性纯红细胞白血病病例,该病例未表达典型的红细胞标志物。该患者出生时白细胞计数高且伴有原始细胞。尽管外周血和骨髓的流式细胞术分析显示有大量CD45阴性细胞群,但我们未发现单克隆性的任何证据。虽然仅通过支持治疗循环中的原始细胞减少,但肝脏肿大伴多个结节,并伴有肝功能衰竭、弥散性血管内凝血和噬血细胞性淋巴组织细胞增生症的发展。肝脏活检标本的病理检查显示为小圆形细胞瘤,几乎所有造血细胞标志物均为阴性,包括经典的红细胞标志物,而CD43、CD71和E-钙黏蛋白(一种早期红细胞标志物上皮钙依赖性黏附蛋白)为阳性,提示这些肿瘤细胞起源于未成熟的成红细胞。我们发现了高β-连环蛋白和c-Myc蛋白表达,这在纯红细胞白血病中此前未见报道。阿糖胞苷暂时缓解了临床症状;然而,患者在8个月大时死于疾病进展。该病例表明,即使在未成熟病例中,E-钙黏蛋白也有助于诊断纯红细胞白血病