폐아세포종 1예

A Case of Pulmonary Blastoma

  • 박강수 (인제대학교 의과대학 상계백병원 내과학교실) ;
  • 함희용 (인제대학교 의과대학 상계백병원 내과학교실) ;
  • 황성보 (인제대학교 의과대학 상계백병원 내과학교실) ;
  • 최수전 (인제대학교 의과대학 상계백병원 내과학교실) ;
  • 이신영 (인제대학교 의과대학 상계백병원 흉부외과학교실) ;
  • 고일향 (인제대학교 의과대학 상계백병원 해부병리과학교실)
  • Park, Kang-Soo (Department of Internal Medicine, Sanggye Paik Hospital, Inje University) ;
  • Hahm, Hee-Yong (Department of Internal Medicine, Sanggye Paik Hospital, Inje University) ;
  • Hwang, Seong-Bo (Department of Internal Medicine, Sanggye Paik Hospital, Inje University) ;
  • Choi, Soo-Jeon (Department of Internal Medicine, Sanggye Paik Hospital, Inje University) ;
  • Lee, Shin-Yeong (Department of Thoracic Surgery, Sanggye Paik Hospital, Inje University) ;
  • Ko, Ill-Hyang (Department of Anatomic Pathology, Sanggye Paik Hospital, Inje University)
  • 발행 : 1994.08.31

초록

최근 저자들은 32세여자에서 발생한 WDFA(Well-differentiated fetal adenocarcinoma)형의 폐아세포종(pulmonary blastoma) 1예를 경험하였기에 보고하는 바이다.

Pulmonary blastoma is a rare lung tumor resembling fetal lung tissue. Pathologically the tumor can be classified to 2 groups, well-differentiated fetal adenocarcinoma(WDFA) and biphasic blastoma. WDFA has more favorable progonosis with fewer metastasis at initial presentation and fewer recurrence after treatment. We experienced a case of pulmonary blastoma in 32-year-old female patient. The patient was refered to our hospital because of abnormal mass shadow in right middle lobe. The diagnosis of pulmonary blastoma(WDFA type, Stage I T2N0M0) was confirmed after right middle lobectomy. We followed up 22 months without an evidence of recurrence.

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