解放军医学院学报
解放軍醫學院學報
해방군의학원학보
Academic Journal of Chinese Pla Medical School
2015年
5期
419-424
,共6页
张秉栋%薛勇敢%刘洪一%王白石%贾宝庆
張秉棟%薛勇敢%劉洪一%王白石%賈寶慶
장병동%설용감%류홍일%왕백석%가보경
甲状腺肿瘤%淋巴瘤%外科手术
甲狀腺腫瘤%淋巴瘤%外科手術
갑상선종류%림파류%외과수술
thyroid neoplasms%lymphoma%surgical procedures,operative
目的:分析原发性甲状腺淋巴瘤的临床表现、诊断、治疗及预后。方法回顾1993年6月-2013年6月解放军总医院收治的原发性甲状腺淋巴瘤20例,分析其临床表现、诊断经过、治疗方案及预后。按疾病分期及是否接受手术分组,分析不同病理类型患者的生存情况。结果1例入院当天因窒息死亡未做治疗,5例通过超声引导穿刺活检明确诊断后接受化疗或化疗+放疗,14例接受单纯手术、手术+化疗或手术+化疗+放疗。中位随访期为41(0~131)个月,随访仍未到达终点。3例黏膜相关淋巴组织淋巴瘤(mucosa-associated lymphoma tissue,MALT)患者长期存活;弥漫大B细胞淋巴瘤(diffuse large B-cell lymphoma,DLBCL)ⅠE期2年、5年生存率均为100%(5例),ⅡE期2年、5年生存率分别为72.9%(6例)和58.3%(5例),ⅠE期DLBCL患者预后优于ⅡE期患者(P=0.048)。DLBCL中接受手术患者2年、5年生存率均为74.1%(7例),未接受手术患者(不包括未治疗患者1例)2年、5年生存率分别为100%(4例)和75.0%(3例)。是否接受手术对DLBCL患者预后无显著影响(P=0.804)。结论 MALT患者经过治疗可长期存活,ⅠE期DLBCL患者预后优于ⅡE期。手术对DLBCL患者预后无显著影响,外科手术的干预应慎重选择。
目的:分析原髮性甲狀腺淋巴瘤的臨床錶現、診斷、治療及預後。方法迴顧1993年6月-2013年6月解放軍總醫院收治的原髮性甲狀腺淋巴瘤20例,分析其臨床錶現、診斷經過、治療方案及預後。按疾病分期及是否接受手術分組,分析不同病理類型患者的生存情況。結果1例入院噹天因窒息死亡未做治療,5例通過超聲引導穿刺活檢明確診斷後接受化療或化療+放療,14例接受單純手術、手術+化療或手術+化療+放療。中位隨訪期為41(0~131)箇月,隨訪仍未到達終點。3例黏膜相關淋巴組織淋巴瘤(mucosa-associated lymphoma tissue,MALT)患者長期存活;瀰漫大B細胞淋巴瘤(diffuse large B-cell lymphoma,DLBCL)ⅠE期2年、5年生存率均為100%(5例),ⅡE期2年、5年生存率分彆為72.9%(6例)和58.3%(5例),ⅠE期DLBCL患者預後優于ⅡE期患者(P=0.048)。DLBCL中接受手術患者2年、5年生存率均為74.1%(7例),未接受手術患者(不包括未治療患者1例)2年、5年生存率分彆為100%(4例)和75.0%(3例)。是否接受手術對DLBCL患者預後無顯著影響(P=0.804)。結論 MALT患者經過治療可長期存活,ⅠE期DLBCL患者預後優于ⅡE期。手術對DLBCL患者預後無顯著影響,外科手術的榦預應慎重選擇。
목적:분석원발성갑상선림파류적림상표현、진단、치료급예후。방법회고1993년6월-2013년6월해방군총의원수치적원발성갑상선림파류20례,분석기림상표현、진단경과、치료방안급예후。안질병분기급시부접수수술분조,분석불동병리류형환자적생존정황。결과1례입원당천인질식사망미주치료,5례통과초성인도천자활검명학진단후접수화료혹화료+방료,14례접수단순수술、수술+화료혹수술+화료+방료。중위수방기위41(0~131)개월,수방잉미도체종점。3례점막상관림파조직림파류(mucosa-associated lymphoma tissue,MALT)환자장기존활;미만대B세포림파류(diffuse large B-cell lymphoma,DLBCL)ⅠE기2년、5년생존솔균위100%(5례),ⅡE기2년、5년생존솔분별위72.9%(6례)화58.3%(5례),ⅠE기DLBCL환자예후우우ⅡE기환자(P=0.048)。DLBCL중접수수술환자2년、5년생존솔균위74.1%(7례),미접수수술환자(불포괄미치료환자1례)2년、5년생존솔분별위100%(4례)화75.0%(3례)。시부접수수술대DLBCL환자예후무현저영향(P=0.804)。결론 MALT환자경과치료가장기존활,ⅠE기DLBCL환자예후우우ⅡE기。수술대DLBCL환자예후무현저영향,외과수술적간예응신중선택。
Objective To analyze the clinical presentation, pathological type, diagnosis, treatment and prognosis of primary thyroid lymphoma (PTL).Methods Clinical data about 20 cases with primary thyroid lymphoma admitted to Chinese PLA General Hospital from June 1993 to June 2013, including clinical manifestation, diagnosis procedure, treatment project and prognosis, were reviewed. According to the stage of primary thyroid lymphoma and whether accepted operation, patients with different pathological types were divided into different groups and their overall survival was analyzed.Results One case died of suffocation without treatment, 5 cases underwent chemotherapy or chemotherapy + radiotherapy after ultrasound guided puncture biopsy for diagnosis, 14 cases underwent operation, operation + chemotherapy or operation + chemotherapy + radiotherapy. The median follow-up time of all patients was 41 months (0 - 131 months), but the follow-up had not reached the end yet. Three MALT patients got long-term survival. The 2-year and 5-year survival rates ofⅠE stage DLBCL were 100% (5 cases) and 100% (5 cases) respectively. The 2-year and 5-year survival rates ofⅡE stage DLBCL were 72.9%(6 cases) and 58.3% (5 cases) respectively. The prognosis of DLBCL patients with stageⅠE was better thanⅡE (P=0.048). The 2-year and 5-year survival rates of DLBCL patients underwent surgery were 74.1% (7 cases) and 74.1% (7 cases) respectively. The 2-year and 5-year survival rates of DLBCL patients without surgery were 100% (4 cases) and 75.0% (3 cases), which showed no significant difference between two groups (P=0.804).Conclusion MALT patients with treatment can get a long-term survival. The prognosis of stageⅠE patients with DLBCL is better than that of stageⅡE patients. Operation has no significant effect on the prognosis of patients with DLBCL. Surgical operation intervention should be chosen carefully.