Clinicopathological analysis of nine cases of small cell carcinoma of the uterine cervix.
- Author:
Guo-hua DENG
1
;
Xun ZHANG
;
Ling-ying WU
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Antineoplastic Combined Chemotherapy Protocols; therapeutic use; CD56 Antigen; metabolism; Carcinoma, Small Cell; metabolism; pathology; therapy; Chromogranin A; metabolism; Cisplatin; therapeutic use; Combined Modality Therapy; Cyclin-Dependent Kinase Inhibitor p16; metabolism; Female; Follow-Up Studies; Humans; Hysterectomy; methods; Lymph Node Excision; Middle Aged; Neoplasm Staging; Nuclear Proteins; metabolism; Paclitaxel; Phosphopyruvate Hydratase; metabolism; Radiotherapy, High-Energy; Survival Rate; Synaptophysin; metabolism; Taxoids; therapeutic use; Thyroid Nuclear Factor 1; Transcription Factors; metabolism; Uterine Cervical Neoplasms; metabolism; pathology; therapy
- From: Chinese Journal of Oncology 2010;32(3):199-202
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the clinicopathologic characteristics, therapy and prognostic factors of small cell carcinoma of the uterine cervix (SCCC).
METHODSNine patients with SCCC underwent radical hysterectomy at the Cancer Hospital of CAMS between 2000 to 2009. Clinical and pathological data were analyzed, and the related literature was reviewed.
RESULTSThe average age of 9 patients was 41 years old. Irregular vaginal bleeding and postcoital spotting were the most common symptoms. According to FIGO staging criteria, six patients were stage Ib1 disease, 2 stage Ib2 and 1 stage IVb. All tumors were composed of small-sized cells with scant cytoplasm, darkly stained round to oval nuclei, finely dispersed chromatin and absence of nucleoli. High mitotic activity and lymphovascular invasion were also common findings. Immunohistochemical staining showed at least three neuroendocrine markers (NSE, CgA, Syn and CD56) were positive in each case. All patients received postoperative chemotherapy, with or without radiotherapy. Seven patients remained alive 6 to 104 months and one died 14 months postoperatively.
CONCLUSIONSCCC is a highly malignant tumor with aggressive behavior. Correct diagnosis of SCCC depends on the combination of light microscopic and immunohistochemical analysis. It is necessary to use multimodality treatment for SCCC, especially the chemotherapy. However, the prognosis is dismal.