Saleh W A, Van de Ven C J, Kim W
Department of Obstetrics and Gynecology, Henry Ford Hospital, Detroit, MI 48202.
Henry Ford Hosp Med J. 1992;40(1-2):136-8.
Peritoneal papillary serous carcinoma is a rare tumor that involves the surface of the pelvic and/or abdominal peritoneum. Long-term survival among patients with this tumor has been rare. Most patients with this cancer have been treated with debulking surgery and postoperative chemotherapy. A case of incompletely resected peritoneal papillary serous carcinoma with a complete response to cisplatin-based chemotherapy is reported. Subsequent laparotomy revealed no residual tumor. This case suggests that primary chemotherapy may be successful in treating unresectable primary papillary serous tumors of the peritoneum.
腹膜乳头状浆液性癌是一种累及盆腔和/或腹腔腹膜表面的罕见肿瘤。该肿瘤患者的长期生存情况较为罕见。大多数此类癌症患者接受了肿瘤减灭术和术后化疗。本文报告了一例腹膜乳头状浆液性癌不完全切除病例,该病例对基于顺铂的化疗有完全反应。随后的剖腹手术显示无残留肿瘤。该病例表明,原发性化疗可能成功治疗无法切除的原发性腹膜乳头状浆液性肿瘤。