Reed K, Ravikumar T S, Gifford R R, Grage T B
Cancer. 1983 Sep 1;52(5):926-8. doi: 10.1002/1097-0142(19830901)52:5<926::aid-cncr2820520530>3.0.co;2-t.
Fanconi's anemia is a rare autosomal recessive disorder which manifests itself in early childhood, presenting as pancytopenia, pigmentation changes, skeletal deformities, small statures and chromosomal aberrations. Most patients ultimately die from sepsis as a result of their hematologic abnormalities, however, some patients live long enough to develop malignancies such as leukemia, hepatocellular carcinomas and squamous cell carcinoma. The association of Fanconi's anemia and squamous cell carcinoma is examined with a report of a patient with Fanconi's anemia and squamous cell carcinoma of the pyriform sinus and hypopharynx.
范科尼贫血是一种罕见的常染色体隐性疾病,在儿童早期发病,表现为全血细胞减少、色素沉着改变、骨骼畸形、身材矮小和染色体畸变。大多数患者最终因血液学异常死于败血症,然而,一些患者存活时间足够长,会发展为恶性肿瘤,如白血病、肝细胞癌和鳞状细胞癌。本文通过报告一例患有范科尼贫血并伴有梨状窦和下咽鳞状细胞癌的患者,对范科尼贫血与鳞状细胞癌的关联进行了研究。