Rodríguez J M, Picardo A, Torres A J, García Calvo M, Ortega L, Martínez S, Balibrea J L
II Cátedra de Cirugía, Hospital Clínico Universidad Complutense, Madrid.
Rev Esp Enferm Dig. 1993 Jul;84(1):56-9.
Peutz-Jeghers syndrome is characterized by hamartomatous polyps in the gastrointestinal tract associated with mucocutaneous melanin spots; the condition is inherited in an autosomic dominant fashion. Although the hamartomatous polyps are not regarded as malignant, there is an association between the Peutz-Jeghers syndrome and the development of carcinomas of the gastrointestinal tract. Similarly, there is an increasing evidence suggesting that hamartomas can give rise to adenocarcinomas. We present a patient with Peutz-Jeghers syndrome who developed an adenocarcinoma in an hamartomatous jejunal polyp.
佩-吉二氏综合征的特征是胃肠道存在错构瘤性息肉,并伴有黏膜皮肤黑色素斑;该病以常染色体显性方式遗传。虽然错构瘤性息肉不被视为恶性,但佩-吉二氏综合征与胃肠道癌的发生之间存在关联。同样,越来越多的证据表明错构瘤可引发腺癌。我们报告了一名患有佩-吉二氏综合征的患者,其在空肠错构瘤性息肉中发生了腺癌。