首页> 外文OA文献 >MALIGNANT ANDROBLASTOMA MANIFESTED PRIMARILY IN THE SPERMATIC CORDS BILATERALLY AND SECONDARILY IN THE LEFT TESTIS : REPORT OF A CASE AND REVIEW OF THE LITERATURE
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MALIGNANT ANDROBLASTOMA MANIFESTED PRIMARILY IN THE SPERMATIC CORDS BILATERALLY AND SECONDARILY IN THE LEFT TESTIS : REPORT OF A CASE AND REVIEW OF THE LITERATURE

机译:在左侧睾丸中双侧和次生主要在雄性睾丸的恶性雄性母细胞瘤中证实:一例病例报告并复习文献

摘要

1. A case of malignant androblastoma manifested primarily in the spermatic cords bilaterally and presumably secondarily in the left testis is presented. The patient, a 50-year-old man, was admitted to our hospital on June 23, 1975, complaining of painless firm masses in the scrotum on both sides of several months duration. There was no gynecomastia. Right inguinal orchidectomy was pereformed on July 3, left inguinal orchidectomy on July 23, and the exstirpation of the metastatic nodule from the skin of the left thigh on August 21, with postoperative chemotherapy with 5FU (250 mg X 23). This patient died on September 15, due to enlarged metastases about 2 months after the first operation. 2. Authors could collect 70 cases of androblastoma from the literature up to the end of 1975 including authors’ case, and a statistical survey was made on 70 cases of androblastomas with a discussion on its clinical features, pathohistology, histogenesis, nomenclature and differential pathohistology. 3. In the age distribution androblastoma showed two peaks, the highest one at the age of 0~1 year and the other at 30~34 years. The youngest is 5 hours old and the oldest 90 years old. 4. Gynecomastia has occurred in 15 of 70 (21.4%) as a whole, in 11 of 60 (18.3%) benign and in 4 of 10 (40%) malignant tumors. 5. Authors summarized 10 cases of malignant androblastoma up to date including authors' case and a discussion was made on its clinical features, pathohistology, therapy, prognosis, metastasis and predisposing factors. 6. In the literature up to date, authors could not find a report of primary androblastoma in the spermatic cord, namely in an extratesticular site. Most probably, the tumor of authors' case originated from aberrant cell elements of the primitive gonadal blastema located in the spermatic cord.
机译:1.恶性母细胞瘤主要表现在双侧精索,左睾丸次之。该患者是一名50岁的男性,于1975年6月23日入院,主诉几个月内阴囊两侧无痛的硬块肿块。没有男性乳房发育。于7月3日进行右腹股沟切除术,于7月23日进行左腹股沟切除术,于8月21日从左大腿皮肤切除转移性结节,并用5FU(250 mg X 23)进行术后化疗。该患者在第一次手术后约2个月因转移扩大而死亡,于9月15日死亡。 2.直到1975年底,作者可以收集包括文献在内的70例雄性母细胞瘤病例,并对70例雄性母细胞瘤进行统计调查,并探讨其临床特征,病理组织学,组织发生,命名和鉴别病理组织学。 。 3.在年龄分布中,成胶质细胞瘤出现两个高峰,最高峰出现在0〜1岁,另一个高峰发生在30〜34岁。最小的年龄为5小时,最大的年龄为90岁。 4.男性乳房发育症总共发生在70例中的15例(占21.4%),60例良性中的11例(占18.3%)和10例恶性肿瘤中的4例(占40%)。 5.作者总结了包括作者病例在内的10例恶性恶性母细胞瘤,并就其临床特征,病理组织学,治疗,预后,转移和诱发因素进行了讨论。 6.在最新文献中,作者找不到在精索中,即在睾丸外部位的原发性成雄细胞瘤的报道。作者病例的肿瘤很可能起源于位于精索中的原始性腺性成纤维细胞的异常细胞成分。

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