Crom D B, Wilimas J A, Green A A, Pratt C B, Jenkins J J, Behm F G
Department of Hematology/Oncology, St. Jude Children's Research Hospital, Memphis, TN 38128.
Med Pediatr Oncol. 1989;17(2):101-4. doi: 10.1002/mpo.2950170206.
From January 1962 to July 1988, 34 infants less than 29 days of age who had cancer were seen at St. Jude Children's Research Hospital (SJCRH). The malignancies in this group consisted of 19 neuroblastomas, 6 leukemias, 3 retinoblastomas, 2 Wilms' tumors, 2 melanomas, and 2 teratomas. Twenty-three patients (68%) are alive and free of disease 2 months to 24 years after diagnosis. We reviewed the presentation and initial symptoms, pathology reports, patient population, associated anomalies, potential genetic influences, and possible perinatal factors. The most common initial symptom was an enlarging abdomen or abdominal mass. Pathological findings were occasionally difficult to interpret; five additional infants who were referred to us did not have malignancies. There was no increased incidence of associated anomalies or perinatal insults. The only genetic factor was retinoblastoma in one parent of each infant diagnosed as having retinoblastoma. The possible etiology of neonatal tumors is discussed.
1962年1月至1988年7月期间,圣裘德儿童研究医院(SJCRH)共收治了34名年龄小于29天的患癌婴儿。该组恶性肿瘤包括19例神经母细胞瘤、6例白血病、3例视网膜母细胞瘤、2例肾母细胞瘤、2例黑色素瘤和2例畸胎瘤。23名患者(68%)在确诊后2个月至24年仍存活且无疾病。我们回顾了临床表现和初始症状、病理报告、患者群体、相关异常、潜在遗传影响以及可能的围产期因素。最常见的初始症状是腹部增大或腹部肿块。病理结果有时难以解释;另外转诊至我院的5名婴儿并无恶性肿瘤。相关异常或围产期损伤的发生率并未增加。唯一的遗传因素是,每例被诊断为视网膜母细胞瘤的婴儿,其父母一方患有视网膜母细胞瘤。本文还讨论了新生儿肿瘤可能的病因。