中华泌尿外科杂志
中華泌尿外科雜誌
중화비뇨외과잡지
CHINESE JOURNAL OF UROLOGY
2014年
12期
921-924
,共4页
陈跃东%吴准%刘菲%曾彦恺%刘荣福%陈斌%王惠强%庄炫%邢金春
陳躍東%吳準%劉菲%曾彥愷%劉榮福%陳斌%王惠彊%莊炫%邢金春
진약동%오준%류비%증언개%류영복%진빈%왕혜강%장현%형금춘
睾丸肿瘤%幼年性黄色肉芽肿%病理学,临床
睪汍腫瘤%幼年性黃色肉芽腫%病理學,臨床
고환종류%유년성황색육아종%병이학,림상
Testicular neoplasms%Juvenile xanthogranuloma%Pathology,clinical
目的 探讨睾丸幼年性黄色肉芽肿的临床及病理特征. 方法 回顾性分析2013年5月收治1例睾丸幼年性黄色肉芽肿患者的诊治情况.患儿6个月,因发现阴囊内肿物2周入院.查体:左侧睾丸大小约2.0 cm×2.0 cm,质地硬,透光试验阴性.甲胎蛋白37.60 μg/L,人绒毛膜促性腺激素<2.0 IU/L.胸部X线片正常.B超检查提示左睾丸内不均质团块,左侧精索增粗,血供丰富.术前诊断为左侧睾丸肿瘤. 结果 行经腹股沟切口手术,术中见左侧精索明显增粗,睾丸弥漫性肿大,质地硬,与正常睾丸组织界限不清,并浸润附睾,附睾头及体部变硬.行高位精索切断睾丸切除术.组织学检查见大量单核细胞、泡沫细胞及炎症细胞(中性粒细胞、嗜酸性粒细胞及淋巴细胞),局灶伴脓肿形成.未见典型的Touton巨细胞.免疫组化显示CD68、CD163阳性,而CD1a阴性.病理诊断为左睾丸幼年性黄色肉芽肿.术后随访10个月未见肿瘤复发. 结论 睾丸幼年性黄色肉芽肿是一种罕见的睾丸良性疾病,临床表现缺乏特异性,组织学特点和免疫组化标志物是诊断该病的主要依据,需与淋巴瘤、白血病及其他睾丸肿瘤相鉴别.
目的 探討睪汍幼年性黃色肉芽腫的臨床及病理特徵. 方法 迴顧性分析2013年5月收治1例睪汍幼年性黃色肉芽腫患者的診治情況.患兒6箇月,因髮現陰囊內腫物2週入院.查體:左側睪汍大小約2.0 cm×2.0 cm,質地硬,透光試驗陰性.甲胎蛋白37.60 μg/L,人絨毛膜促性腺激素<2.0 IU/L.胸部X線片正常.B超檢查提示左睪汍內不均質糰塊,左側精索增粗,血供豐富.術前診斷為左側睪汍腫瘤. 結果 行經腹股溝切口手術,術中見左側精索明顯增粗,睪汍瀰漫性腫大,質地硬,與正常睪汍組織界限不清,併浸潤附睪,附睪頭及體部變硬.行高位精索切斷睪汍切除術.組織學檢查見大量單覈細胞、泡沫細胞及炎癥細胞(中性粒細胞、嗜痠性粒細胞及淋巴細胞),跼竈伴膿腫形成.未見典型的Touton巨細胞.免疫組化顯示CD68、CD163暘性,而CD1a陰性.病理診斷為左睪汍幼年性黃色肉芽腫.術後隨訪10箇月未見腫瘤複髮. 結論 睪汍幼年性黃色肉芽腫是一種罕見的睪汍良性疾病,臨床錶現缺乏特異性,組織學特點和免疫組化標誌物是診斷該病的主要依據,需與淋巴瘤、白血病及其他睪汍腫瘤相鑒彆.
목적 탐토고환유년성황색육아종적림상급병리특정. 방법 회고성분석2013년5월수치1례고환유년성황색육아종환자적진치정황.환인6개월,인발현음낭내종물2주입원.사체:좌측고환대소약2.0 cm×2.0 cm,질지경,투광시험음성.갑태단백37.60 μg/L,인융모막촉성선격소<2.0 IU/L.흉부X선편정상.B초검사제시좌고환내불균질단괴,좌측정색증조,혈공봉부.술전진단위좌측고환종류. 결과 행경복고구절구수술,술중견좌측정색명현증조,고환미만성종대,질지경,여정상고환조직계한불청,병침윤부고,부고두급체부변경.행고위정색절단고환절제술.조직학검사견대량단핵세포、포말세포급염증세포(중성립세포、기산성립세포급림파세포),국조반농종형성.미견전형적Touton거세포.면역조화현시CD68、CD163양성,이CD1a음성.병리진단위좌고환유년성황색육아종.술후수방10개월미견종류복발. 결론 고환유년성황색육아종시일충한견적고환량성질병,림상표현결핍특이성,조직학특점화면역조화표지물시진단해병적주요의거,수여림파류、백혈병급기타고환종류상감별.
Objective To discuss the clinical and pathological features of the juvenile xanthogranuloma of testis.Methods A case of the juvenile xanthogranuloma of testis was reported.A 6-month-old boy presented with scrotal mass for 2 weeks before admission.Physical examination revealed that the left testis was hard with the size of 2.0 cm×2.0 cm and the serum alpha-fetoprotein was 37.60 μg/L.Chest X-ray and serum human chorionic gonadotropin investigations were normal.B-ultrasound examination showed a solid mass of uniform homogeneity in the left testis,with rich blood supply.Results The patient underwent operation after inguinal incision under general anaesthesia.During operation the left spermatic was augmented,and the mass was infiltrated into the whole testis and epididydis,and an inguinal orchiectomy was competed.Histopathological examination revealed that the lesion was intratesticular and involvement of the epididymis,predominantly occupied with an infiltrative pattern of by mononuclear cells,foamy cells and inflammatory cells (neutrophils,eosinophils,lymphocytes),without Touton giant cells.Immunohistochemical examination revealed positive for CD68 and CD163,and negative for CD1a.The pathological result was juvenile xanthogranuloma.During the follow-up period for 10 months,no recurrence was recorded.Conclusions Juvenile xanthogranuloma of the testis is an extremely rare benign disease lack of special feature in clinical manifestation.The diagnosis mainly depends on histological features and special markers in immunohistochemistry.Differential diagnosis should be made among leukemia,lymphoma and other distinctive neoplasms.