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Testicular thecoma in an 11-year-old boy with nevoid basal-cell carcinoma syndrome (Gorlin syndrome).

机译：一名11岁男孩患有无基底细胞癌综合征（Gorlin综合征）的睾丸昏迷。

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摘要

We report a case of testicular thecoma in an 11-year-old Japanese boy with nevoid basal-cell carcinoma syndrome (Gorlin syndrome). He presented with left testicular swelling and underwent a radical orchiectomy on suspicion of a malignant paratesticular tumor. The tumor arose from the testis exophytically and was diagnosed as a thecoma histopathologically. Ovarian thecoma-fibroma group tumors are closely associated with Gorlin syndrome or with abnormalities in PTCH, a candidate gene for the syndrome. The occurrence of an extremely rare testicular thecoma in this case (the second in the literature) suggests that such an etiological association may also exist in the pathogenesis of testicular tumors.

机译：我们报告了一个11岁的日本男孩患睾丸肉瘤的情况，该男孩患有无基底细胞癌综合征（Gorlin综合征）。他表现出左睾丸肿胀，并因怀疑患有恶性副睾丸肿瘤而接受了根治性睾丸切除术。肿瘤由睾丸外生而来，从组织病理学上被诊断为昏迷。卵巢肿瘤性纤维瘤组肿瘤与戈林综合征或PTCH异常密切相关，PTCH是该综合征的候选基因。在这种情况下（文献中的第二例）极少见的睾丸瘤的发生表明，这种病因学关联也可能存在于睾丸肿瘤的发病机理中。

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作者
Ueda Masakatsu; Kanematsu Akihiro; Nishiyama Hiroyuki; Yoshimura Koji; Watanabe Kenichiro; Yorifuji Tohru; Mikami Yoshiki; Kamoto Toshiyuki; Ogawa Osamu;
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年度 2010
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正文语种 eng
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专利

1. Multiple, Multiloculated, and Recurrent Keratocysts of the Mandible and Maxilla in Association with Gorlin-Goltz (Nevoid Basal-Cell Carcinoma) Syndrome: A Pediatric Case Report and Follow-up over 5 Years [J] . P. Santander, E. M. C. Schwaibold, F. Bremmer, Case Reports in Dentistry . 2018,第1期

机译：下颌骨和上颌骨的多发性，多发性和复发性角膜囊肿与戈林-戈尔茨氏综合征（无基底细胞癌）综合征相关：小儿病例报告和五年以上随访
2. The naevoid basal-cell carcinoma syndrome (Gorlin syndrome) is a chromosomal instability syndrome. [J] . Shafei-Benaissa E, Savage JR, Babin P, Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects . 1998,第2期

机译：无回避型基底细胞癌综合征（Gorlin综合征）是一种染色体不稳定综合征。
3. New mutation of the PTCH gene in nevoid basal-cell carcinoma syndrome with West syndrome. [J] . Tachi N, Fujii K, Kimura M, Pediatric neurology . 2007,第5期

机译：伴有West综合征的无基底细胞癌综合征中PTCH基因的新突变。
4. A novel mutation of the PTCH1 gene activates the Shh/Gli signaling pathway in a Chinese family with nevoid basal cell carcinoma syndrome [C] . Tingting Zhang, Mingjie Chen, Yan Lü, Academic Committee Conference of Shanghai key lab of stomatology . 2011

机译：PTCH1基因的新型突变激活了中国患有避免基底细胞癌综合征的中国家庭的Shh / Gli信号通路
5. The relationship of repetitive behavior and sensory behavior to parenting stress in mothers of boys with autism and mothers of boys with fragile X syndrome [D] . Richardson, Lolita Lisa 2010

机译：自闭症男孩和易碎X综合征男孩的重复行为和感觉行为与父母压力的关系
6. Multiple Multiloculated and Recurrent Keratocysts of the Mandible and Maxilla in Association with Gorlin-Goltz (Nevoid Basal-Cell Carcinoma) Syndrome: A Pediatric Case Report and Follow-up over 5 Years [O] . P. Santander, E. M. C. Schwaibold, F. Bremmer, 2018

机译：下颌骨和上颌骨的多发性多发性和复发性角膜囊肿与戈林-戈尔茨综合征（无基底细胞癌）综合征相关：儿童病例报告和5年以上随访
7. Nevoid Basal-Cell Carcinoma (Gorlin) Syndrome [O] . J Gordon Millichap 1996

机译：Nevoid基础细胞癌（Gorlin）综合征

Testicular thecoma in an 11-year-old boy with nevoid basal-cell carcinoma syndrome (Gorlin syndrome).

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