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睾丸原发性类癌肿瘤:29 例临床病理研究。

Primary carcinoid tumors of the testis: a clinicopathologic study of 29 cases.

机构信息

Departments of Pathology, VA Maryland Health Care System, USA.

出版信息

Am J Surg Pathol. 2010 Apr;34(4):519-24. doi: 10.1097/PAS.0b013e3181d31f33.

Abstract

Testicular carcinoid tumors are rare with only limited studies. We identified 29 primary testicular carcinoid cases from 7 academic institutions. Patients ranged in age from 12 to 65 years old (mean 36). The most common presenting symptom was the sole finding of either a testicular mass or swelling seen in 15/24 cases with available information. The next most common mode of presentation was as an incidental finding seen in 6 cases. Two patients had carcinoid syndrome including diarrhea, hot flashes, and palpitations. Nineteen were pure carcinoid tumors, 3 were associated with cystic teratoma, 2 with cysts lacking epithelial lining, 4 with epidermoid cyst, and 1 with dermoid cyst. The mean size was 2.5 cm. All 29 primary carcinoids lacked associated intratubular germ cell neoplasia, unclassified type. Mitotic figures were rare in primary carcinoid tumors with only 3 cases showing more than 2 per 10 HPF; necrosis was found in only 1 case. Random scattered mild to moderate nuclear atypia was seen in 12/29 cases. Of the 28 cases found premortem, treatment included focal excision in 3 patients and radical orchiectomy in 25 patients. Follow-up, available in 24 cases, ranged from 1 to 228 months (mean 52.7 mo); of the 20 patients with testicular typical carcinoid tumors found premortem, all were alive at last follow-up without recurrences or metastases. Of the 4 patients with a primary atypical carcinoid tumor, 1 at the time of diagnosis had retroperitoneal and lung metastases who after chemotherapy underwent resection of the retroperitoneal tumor showing metastatic yolk sac tumor and embryonal carcinoma. After resection, serum AFP levels remained elevated and the patient is scheduled for salvage chemotherapy and bone marrow transplant. The other 2 patients with atypical carcinoid and follow-up had no evidence of disease at 68 and 114 months. Most primary carcinoid tumors of the testis have a benign clinical course even if associated with epidermoid/dermoid cysts, or histologically mature teratoma. However, lesions with the morphology of atypical carcinoid can occasionally exhibit metastatic spread.

摘要

睾丸类癌肿瘤罕见,相关研究有限。我们从 7 家学术机构中确定了 29 例原发性睾丸类癌病例。患者年龄在 12 岁至 65 岁之间(平均 36 岁)。最常见的表现为 15/24 例有可用信息的患者仅表现为睾丸肿块或肿胀。下一个最常见的表现模式是 6 例偶然发现。2 例患者出现类癌综合征,包括腹泻、潮热和心悸。19 例为单纯类癌肿瘤,3 例与囊性畸胎瘤有关,2 例与无上皮衬里的囊肿有关,4 例与表皮样囊肿有关,1 例与皮样囊肿有关。肿瘤平均大小为 2.5cm。所有 29 例原发性类癌均缺乏相关的未分类型睾丸内生殖细胞肿瘤。原发性类癌肿瘤的有丝分裂象罕见,仅 3 例每 10HPF 超过 2 个;仅 1 例有坏死。12/29 例可见随机散在的轻度至中度核异型性。28 例生前发现的病例中,治疗包括 3 例局部切除术和 25 例根治性睾丸切除术。24 例可获得随访,随访时间为 1 至 228 个月(平均 52.7 个月);20 例生前发现的睾丸典型类癌肿瘤患者均存活,无复发或转移。4 例原发性非典型类癌患者中,1 例诊断时存在腹膜后和肺部转移,化疗后行腹膜后肿瘤切除术,显示转移的卵黄囊瘤和胚胎癌。切除后,血清 AFP 水平仍升高,患者计划接受挽救化疗和骨髓移植。另外 2 例非典型类癌患者和随访患者在 68 个月和 114 个月时均无疾病证据。大多数睾丸类癌肿瘤具有良性临床过程,即使与表皮样/皮样囊肿或组织学成熟的畸胎瘤有关。然而,具有非典型类癌形态的病变偶尔会出现转移扩散。

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