- Author:
Lai XU
1
;
Yu-pei ZHAO
;
Wei-bin WANG
;
Tai-ping ZHANG
;
Quan LIAO
;
Ge CHEN
;
Li ZHOU
;
Hong SHU
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adult; Age of Onset; Aged; Carcinoma, Medullary; classification; genetics; pathology; Carcinoma, Neuroendocrine; Female; Genetic Diseases, Inborn; pathology; Humans; Male; Middle Aged; Prognosis; Retrospective Studies; Survival Rate; Thyroid Neoplasms; classification; genetics; pathology; Young Adult
- From: Acta Academiae Medicinae Sinicae 2012;34(4):401-404
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo study the clinical characteristics and outcomes of the hereditary medullary thyroid carcinoma (HMTC) and the sporadic medullary thyroid carcinoma (SMTC).
METHODSThe clinical data of 78 patients with medullary thyroid carcinoma who underwent surgery in our hospital between July 1980 and May 2011 were retrospectively analyzed.
RESULTSOf these 78 patients, there were 23 HMTC cases and 55 SMTC cases. The HMTC group was significantly younger age of onset [(36.4±13.5) years vs. (46.6±11.2) years, P<0.01] and a lower pre/post-operative serum calcitonin levels [(850.4±110.20) ng/L vs. (1450.4±118.3) ng/L, P<0.01 and (410.8±133.2) ng/L vs. (1585.4±129.5) ng/L, P<0.01] than the SMTC group. In addition, the mean tumor diameter was also significantly smaller in the HMTC group (14.3 mm vs. 21.0 mm in SMTC group, P<0.05). Tumor multifocality was seen in a significantly higher proportion of HMTC cases compared with the SMTC cases (56.6% vs. 29.1%, P<0.05). The overall 10-year survival was 100% in HMTC group and 80.2% in SMTC group (P<0.05).
CONCLUSIONHMTC has a better prognosis than SMTC.