Akbulut Metin, Kelten Canan, Bir Ferda, Soysal Mehmet Emin, Duzcan Suleyman Ender
Pamukkale University School of Medicine, Department of Pathology, Morfoloji Binasi, Kinikli 20070, Denizli, Turkey.
Gynecol Oncol. 2007 Apr;105(1):248-51. doi: 10.1016/j.ygyno.2006.11.024. Epub 2007 Jan 12.
Psammocarcinoma is a rare variant of serous carcinoma arising from either ovary or peritoneum. Although behavior of tumor is uncertain, it has been suggested to be similar to serous carcinomas of low malignant potential.
A 67-year-old woman was admitted with an abnormal vaginal bleeding and abdomino-pelvic pain. Computed tomography showed a heavily calcified rectovaginal mass that was histologically characterized by numerous psammoma bodies and low-grade cytological features. Following the primary surgery, the patient received 9 cycles of chemotherapy. Five years later, she presented with diffuse recurrence and 1 year later, with metastasis to the vertebra.
Although psammocarcinoma is known to behave in a more indolent course, clinicians should be aware that patients with this disease may have a clinically aggressive, recurrent, and metastatic tumor that necessitated systemic therapy.
砂粒体癌是一种罕见的浆液性癌变异型,起源于卵巢或腹膜。尽管肿瘤的行为尚不确定,但有人认为它与低恶性潜能的浆液性癌相似。
一名67岁女性因异常阴道出血和腹盆腔疼痛入院。计算机断层扫描显示直肠阴道有一个大量钙化的肿块,组织学特征为大量砂粒体和低级别细胞学特征。初次手术后,患者接受了9个周期的化疗。五年后,她出现弥漫性复发,一年后发生椎体转移。
尽管已知砂粒体癌病程较为惰性,但临床医生应意识到,患有这种疾病的患者可能会出现具有临床侵袭性、复发性和转移性的肿瘤,需要进行全身治疗。