Ishtiaq Osama, Baqai Haider Z, Anwer Faiz, Hussain Nisar
Medical Unit II, Holy Family Hospital, Rawalpindi.
J Ayub Med Coll Abbottabad. 2004 Jan-Mar;16(1):8-13.
There has been little systematic study on the clinical spectrum of pancytopenia. This study was done to describe the etiology, presentation and outcome of patients with pancytopenia presenting in a general medical ward.
Hundred patients with pancytopenia were included in the study from October 2001 to October 2002. Patients on cancer chemotherapy were excluded. Blood counts, bone marrow examinations and trephine biopsies were performed according to standard methods.
In all cases, megaloblastic anemia constituted the largest group (n = 39), and also seen in conjunction with hemolytic anemia and septicemia. Hypersplenism secondary to portal hypertension (cirrhosis) was the second most common diagnosis (n = 19). Aplastic anemia, septicemia and myelodysplasia were other common causes. Two patients were the suspected cases of viral hemorrhagic fever. Thirteen (13%) patients expired. Absolute neutrophil count (ANC) less than 500/microliter was seen in 14 (14%) patients, among which 6 (15.3%) had megaloblastic anemia, 3 (37.5%) had aplastic anemia, and 2 (40%) had myelodysplasia. Eleven patients with platelet counts < or = 10 x 10(9)/L, 6 (54.5%) presented with bleeding; and 2 of these 8 had aplastic anemia and 1 patient with megaloblastic anemia. MCV values > 100 fL and > 110 fL were more frequent in patients with megaloblastic anemia with most prominent anisopoikilocytosis, microcytosis and fragmented RBCs. Macrocytosis was noted in 35 (89.7%) patients with megaloblastic anemia and 12 (63.1%) with hypersplenism, 4 (50%) with aplastic anemia. Hypersegmented neutrophils were noted in the blood films of 36 (92.3%) patients with megaloblastic anemia.
Megaloblastic anemia, hypersplenism and aplastic anemia are the common causes of pancytopenia in our study.
关于全血细胞减少的临床谱,系统研究较少。本研究旨在描述综合内科病房中全血细胞减少患者的病因、临床表现及转归。
2001年10月至2002年10月纳入100例全血细胞减少患者。排除接受癌症化疗的患者。按照标准方法进行血细胞计数、骨髓检查及骨髓活检。
所有病例中,巨幼细胞贫血患者最多(n = 39),也可见于合并溶血性贫血和败血症的情况。门静脉高压(肝硬化)继发的脾功能亢进是第二常见诊断(n = 19)。再生障碍性贫血、败血症和骨髓增生异常综合征是其他常见病因。2例患者疑似病毒出血热。13例(13%)患者死亡。14例(14%)患者中性粒细胞绝对值(ANC)低于500/微升,其中6例(15.3%)为巨幼细胞贫血,3例(37.5%)为再生障碍性贫血,2例(40%)为骨髓增生异常综合征。11例血小板计数≤10×10⁹/L的患者中,6例(54.5%)有出血表现;这8例中有2例为再生障碍性贫血,1例为巨幼细胞贫血。巨幼细胞贫血患者中,平均红细胞体积(MCV)值>100 fL和>110 fL更为常见,且大多伴有显著的异形红细胞增多、小红细胞症和破碎红细胞。35例(89.7%)巨幼细胞贫血患者、12例(63.1%)脾功能亢进患者及4例(50%)再生障碍性贫血患者出现大红细胞症。36例(92.3%)巨幼细胞贫血患者的血片中可见核分叶过多的中性粒细胞。
在我们的研究中,巨幼细胞贫血、脾功能亢进和再生障碍性贫血是全血细胞减少的常见病因。