Clark R H, Taylor L L, Wells R J
Pediatrics. 1984 Mar;73(3):324-6.
The case of a patient with ecchymosis, hepatomegaly, leukocytosis, thrombocytopenia, and anemia at birth is presented. Throughout his course, thrombocytopenia, anemia, and leukocytosis without a marked increase in the number of blast forms in either peripheral blood or bone marrow persisted until the patient developed a blast crisis shortly before his death at age 4 months. This patient is the youngest reported to have the juvenile form of chronic myelogenous leukemia and the first that in the present era can be considered congenital in origin.
本文介绍了一名出生时即出现瘀斑、肝肿大、白细胞增多、血小板减少和贫血的患者病例。在其整个病程中,血小板减少、贫血和白细胞增多持续存在,外周血或骨髓中的原始细胞数量均无明显增加,直至该患者在4个月大死亡前不久发生原始细胞危象。该患者是有报道的最年轻的青少年型慢性粒细胞白血病患者,也是当代首例可认为起源于先天性的病例。