Emadi Ashkan, Burns Kathleen H, Confer Bradley, Borowitz Michael J, Streiff Michael B
Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD 21231-1000, USA.
Acta Haematol. 2008;119(3):169-72. doi: 10.1159/000134222. Epub 2008 May 21.
Pancytopenia is an uncommon manifestation of cystinosis, a congenital lysosomal storage disease. We describe a 34-year-old patient with nephropathic cystinosis with multisystem involvement who developed progressive bone marrow failure after renal transplantation. Bone marrow examination demonstrated widespread deposition of cystine crystals in histiocytes and in the background. We review the literature on the hematologic manifestations of cystinosis and discuss the available treatment options for patients with bone marrow failure secondary to cystine accumulation. The availability of effective oral therapy and the limited activity of hematopoietic growth factors in these patients highlight the importance of bone marrow examination early in the evaluation of cystinosis patients with abnormal blood counts.
全血细胞减少是胱氨酸贮积症(一种先天性溶酶体贮积病)的罕见表现。我们描述了一名34岁患有肾病性胱氨酸贮积症且多系统受累的患者,其在肾移植后出现进行性骨髓衰竭。骨髓检查显示组织细胞及背景中广泛存在胱氨酸晶体沉积。我们回顾了关于胱氨酸贮积症血液学表现的文献,并讨论了继发于胱氨酸蓄积的骨髓衰竭患者的可用治疗方案。有效的口服治疗方法的可及性以及造血生长因子在这些患者中的有限活性凸显了在评估血细胞计数异常的胱氨酸贮积症患者时早期进行骨髓检查的重要性。