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遗传性椭园形红细胞增多症(hereolitaryelliplocytosis.H E),我国已有近20例报道,而同时伴有急淋L_2型,国内未见报道。我院发现一例报告如下。 患者王某,男性,26岁,以头晕乏力一周就诊,伴鼻衄,齿龈出血。无明显原因,素常感冒,常服用“安乃近”,否认毒物及放射线接触史。查体:一般情况好,轻度贫血貌,四肢可见散在的皮下瘀斑,出血点,表浅淋巴结未见肿大,心肺(-),腹平软,肝脾未触及,神经系统未见异常,无骨骼痛。实验室检查:Hb98g/L,RBC 3.32×10~(12)/L,WBC2.65×10~9/L,BPC 23×10~9/L,分类:中性粒0.32,原淋0.01,幼淋0.01,
Hereditary hypersplenism (hereolitaryelliplocytosis.H E), China has nearly 20 cases reported, while accompanied by acute lymphoblastic L_2 type, no domestic report. Our hospital found a case report as follows. Patient Wang, male, 26 years old, dizziness, fatigue week treatment, with epistaxis, gum bleeding. No obvious reason, common cold, often taking “metamizole”, denied the history of poison and radiation exposure. Physical examination: the general situation is good, mild anemia, scattered subcutaneous ecchymosis visible limbs, bleeding, superficial lymph node enlargement, cardiopulmonary (-), abdominal soft, liver and spleen not touched, the nervous system was normal , No bone pain. Laboratory tests: Hb98g / L, RBC 3.32 × 10-12 / L, WBC2.65 × 10 ~ 9/L, BPC 23 × 10 ~ 9 / L, Category: Neutrophil 0.32, 0.01,