首页> 外文期刊>The Journal of Urology >Clinical and pathological features associated with the testicular tumor of the adrenogenital syndrome.
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Clinical and pathological features associated with the testicular tumor of the adrenogenital syndrome.

机译:与肾上腺皮质综合征睾丸肿瘤相关的临床和病理特征。

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PURPOSE: Testicular tumor of the adrenogenital syndrome is a rare clinical entity found in young men with endocrine disorders. Histologically it resembles Leydig cell tumor. We 1) reviewed the clinical features of testicular tumor of the adrenogenital syndrome and 2) determined if special histopathological features of the tumor and synaptophysin reactivity could distinguish testicular tumor of the adrenogenital syndrome from Leydig cell tumor. MATERIALS AND METHODS: We reviewed the medical and pathological records for all patients with testicular tumor of the adrenogenital syndrome seen at our institution from 1978 to 2004. These tumors were examined by histological and immunophenotypic methods for comparison to Leydig cell tumor. RESULTS: A total of 14 males with an endocrine disorder had pathological evidence of testicular tumor of the adrenogenital syndrome. These tumors were often bilateral (93% or 13 of 14 cases), associated with pain (92% or 12 of 13) and refractory to medical management with high dose exogenous steroids (93% or 13 of 14). Testicular tumor of the adrenogenital syndrome was managed by tumor enucleation in 7 patients (54%) and by radical orchiectomy in 6 (46%). All patients had resolution of pain at 3-month followup. Upon histological review features found to be more common to testicular tumor of the adrenogenital syndrome compared with Leydig cell tumor were nuclear pleiomorphism, low mitotic activity, extensive fibrosis, lymphoid aggregates, adipose metaplasia and prominent lipochrome pigment. Synaptophysin (ICN, Costa Mesa, California) reactivity was strong in testicular tumor of the adrenogenital syndrome but rarely observed in Leydig cell tumor. CONCLUSIONS: In our series medical treatment failed in patients with testicular tumor of the adrenogenital syndrome and conservative surgical therapy was possible in select individuals. We identified special histopathological and immunophenotypic features, including synaptophysin staining, which distinguish testicular tumor of the adrenogenital syndrome from Leydig cell tumor.
机译:目的:肾上腺皮质综合征的睾丸肿瘤是在患有内分泌失调的年轻男性中发现的罕见临床实体。从组织学上讲,它类似于Leydig细胞肿瘤。我们1)回顾了肾上腺源性综合征的睾丸肿瘤的临床特征,以及2)确定了肿瘤的特殊组织病理学特征和突触素反应性是否可以将Leydig细胞瘤与肾上腺源性综合征的睾丸肿瘤区分开。材料与方法:我们回顾了从1978年至2004年在本院就诊的所有患有肾上腺综合征的睾丸肿瘤患者的医学和病理记录。这些肿瘤通过组织学和免疫表型方法进行了检查,以与Leydig细胞肿瘤进行比较。结果:总共14名内分泌失调的男性具有肾上腺源性综合征的睾丸肿瘤的病理学证据。这些肿瘤通常是双侧的(93%或14例中的13例),伴有疼痛(92%或12例中的12例),并且对高剂量外源性类固醇的药物治疗无效(93%或14例中的13例)。肾上腺综合症的睾丸肿瘤通过肿瘤摘除术治疗7例(54%),而根治性睾丸切除术治疗6例(46%)。所有患者在3个月的随访中均缓解了疼痛。经组织学检查发现,与Leydig细胞肿瘤相比,肾上腺生殖器综合征的睾丸肿瘤更常见的特征是核多型性,有丝分裂活性低,广泛的纤维化,淋巴样聚集,脂肪化生和突出的脂质色素。突触素(ICN,哥斯达黎加梅萨,加利福尼亚州)的反应性在肾上腺源性综合征的睾丸肿瘤中很强,但在莱迪希德细胞瘤中很少观察到。结论:在我们的系列研究中,肾上腺综合症睾丸肿瘤患者的药物治疗失败,某些患者可以进行保守的手术治疗。我们确定了特殊的组织病理学和免疫表型特征,包括突触素染色,可以将肾上腺源性综合征的睾丸肿瘤与Leydig细胞肿瘤区分开。

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