临床与实验病理学杂志
臨床與實驗病理學雜誌
림상여실험병이학잡지
CHINESE JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY
2015年
5期
492-496
,共5页
税迎春%王建军%管群%王海%李万春%王建东%刘琦%石群立
稅迎春%王建軍%管群%王海%李萬春%王建東%劉琦%石群立
세영춘%왕건군%관군%왕해%리만춘%왕건동%류기%석군립
卵巢肿瘤%小细胞癌%高钙血症%急性肾功能不全%免疫组织化学
卵巢腫瘤%小細胞癌%高鈣血癥%急性腎功能不全%免疫組織化學
란소종류%소세포암%고개혈증%급성신공능불전%면역조직화학
ovarian neoplasm%small cell carcinoma%hypercalcaemia%acute renal dysfunction%immunohistochemistry
目的:探讨卵巢高钙血症型小细胞癌( ovarian small cell carcinoma hypercalcemic type, OSCCHT)伴急性肾功能不全的临床病理学特征、诊断及鉴别诊断。方法回顾性分析1例OSCCHT伴急性肾脏功能不全患者的临床资料、组织学形态、免疫表型、超微结构等,并复习相关文献。结果患者女性,29岁。因无明显诱因出现食欲不振伴明显消瘦1个月余。实验室检查示肾功能异常;影像学示盆腔肿块,考虑附件来源。血液透析肾功能部分恢复后行手术。右侧卵巢见一12 cm ×10 cm ×10 cm大小肿瘤,镜下见瘤细胞呈弥漫实性分布,被纤维条索分割成多结节状,部分细胞间可见小滤泡样、假腺样结构,腔内可见嗜酸性分泌物,瘤细胞中等偏大,胞质嗜酸性,核圆形、卵圆形,核呈空泡状,核质比高,核分裂象多见。免疫表型:癌细胞EMA和CK、C-erbB-2均(+),CA125(灶+),ER、PR、Syn、CgA、PTH、Inhibin、CD99、AFP、PLAP、CD30和CD20均(-),Ki-67增殖指数约60%。结论 OSCCHT临床少见,同时伴急性肾脏功能不全更为罕见。 OSCCHT是一种进展迅速、高度恶性的卵巢恶性肿瘤,确诊主要根据其临床特点(血钙升高等)、病理学特征及免疫表型,必要时可结合电镜和分子生物学检测辅助诊断。
目的:探討卵巢高鈣血癥型小細胞癌( ovarian small cell carcinoma hypercalcemic type, OSCCHT)伴急性腎功能不全的臨床病理學特徵、診斷及鑒彆診斷。方法迴顧性分析1例OSCCHT伴急性腎髒功能不全患者的臨床資料、組織學形態、免疫錶型、超微結構等,併複習相關文獻。結果患者女性,29歲。因無明顯誘因齣現食欲不振伴明顯消瘦1箇月餘。實驗室檢查示腎功能異常;影像學示盆腔腫塊,攷慮附件來源。血液透析腎功能部分恢複後行手術。右側卵巢見一12 cm ×10 cm ×10 cm大小腫瘤,鏡下見瘤細胞呈瀰漫實性分佈,被纖維條索分割成多結節狀,部分細胞間可見小濾泡樣、假腺樣結構,腔內可見嗜痠性分泌物,瘤細胞中等偏大,胞質嗜痠性,覈圓形、卵圓形,覈呈空泡狀,覈質比高,覈分裂象多見。免疫錶型:癌細胞EMA和CK、C-erbB-2均(+),CA125(竈+),ER、PR、Syn、CgA、PTH、Inhibin、CD99、AFP、PLAP、CD30和CD20均(-),Ki-67增殖指數約60%。結論 OSCCHT臨床少見,同時伴急性腎髒功能不全更為罕見。 OSCCHT是一種進展迅速、高度噁性的卵巢噁性腫瘤,確診主要根據其臨床特點(血鈣升高等)、病理學特徵及免疫錶型,必要時可結閤電鏡和分子生物學檢測輔助診斷。
목적:탐토란소고개혈증형소세포암( ovarian small cell carcinoma hypercalcemic type, OSCCHT)반급성신공능불전적림상병이학특정、진단급감별진단。방법회고성분석1례OSCCHT반급성신장공능불전환자적림상자료、조직학형태、면역표형、초미결구등,병복습상관문헌。결과환자녀성,29세。인무명현유인출현식욕불진반명현소수1개월여。실험실검사시신공능이상;영상학시분강종괴,고필부건래원。혈액투석신공능부분회복후행수술。우측란소견일12 cm ×10 cm ×10 cm대소종류,경하견류세포정미만실성분포,피섬유조색분할성다결절상,부분세포간가견소려포양、가선양결구,강내가견기산성분비물,류세포중등편대,포질기산성,핵원형、란원형,핵정공포상,핵질비고,핵분렬상다견。면역표형:암세포EMA화CK、C-erbB-2균(+),CA125(조+),ER、PR、Syn、CgA、PTH、Inhibin、CD99、AFP、PLAP、CD30화CD20균(-),Ki-67증식지수약60%。결론 OSCCHT림상소견,동시반급성신장공능불전경위한견。 OSCCHT시일충진전신속、고도악성적란소악성종류,학진주요근거기림상특점(혈개승고등)、병이학특정급면역표형,필요시가결합전경화분자생물학검측보조진단。
Purpose To investigate the clinicopathlogical characteristics, diagnosis and differential diagnosis of ovarian small cell car-cinoma hypercalcemic type ( OSCCHT) associated with acute renal dysfunction. Methods A case of OSCCHT associated with acute renal dysfunction was reported. The clinical and pathologic data, treatment and pathological examinations were analyzed and the related literatures were reviewed. Results A 29-year-olds women was presented to hospital with inappetence and significant weight loss for 2 months. The laboratory examination showed abnormal renal function, and pelvic cavity mass, possibly coming from adnexa of the uterus was seen by radiography. Serum levels showed significantly increased serum calcium with acute renal dysfunction. An emergency opera-tion was performed just after renal function partially recovered by 2 times hemodialysis. During surgery, right ovary tumor with a size of 12 cm × 10 cm × 10 cm was inspected. Microscopically, the tumor cells were arranged in a diffuse solid pattern, mutiple nodules were separated by fibrous tissue. some small folliculars and pseudoglandular cavities with acidophilia secretion within nodules could been ob-served. Tumor cells were medium to large with eosinophilic cytoplasm, round or oval vesicular nucleus, increased karyoplasmic ratio and pathologic mitosis. Immunohistochemistry revealed that the tumor cells expressed EMA, CKpan, C-erbB-2 ( +) , CA125 ( focal+) and Ki-67 proliferation index was about 60%, while ER, PR, Syn, CgA, PTH, Inhibin, CD99, AFP, PLAP, CD30 and CD20 were not expressed. Conclusion Ovarian small cell carcinoma hypercalcemic type with acute renal dysfunction is a very rare with a rapidly progressive and highly malignant tumor. The final diagnosis mainly lies on clinical information ( hypercalcaemia) , morphology and immunohistochemistry, combined with electron microscopy and molecular biological detection when necessary.