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[睾丸生殖细胞肿瘤:根据世界卫生组织命名法对552例病例的组织学分类]

[Germ cell tumors of testis: histological classification of 552 cases according to the WHO-nomenclature].

作者信息

Stiller D, Katenkamp D, Pressler H, Kosmehl H

出版信息

Zentralbl Allg Pathol. 1983;128(1-2):85-100.

PMID:6637191
Abstract

Using the WHO-nomenclature 552 germ cell tumors of testis were reclassified. The analysis revealed the following: germ cell tumors occur in early childhood at the age of 3 months to 3 years, in adult hood (26-35) the occurrence shows a peak, and in old aged men only some tumors are registered. No germ cell was found between 4 to 13 years. Our material comprised 245 seminomas (44.4%) and 307 non-seminomatous germ cell tumors (55.6%). In the group of tumors of one histologic type, 245 cases of seminomas represent the main part. The following subgroups were recognized: typical seminomas--229 cases (93.5%), spermatocytic seminomas--9 cases (3.7%), and anaplastic seminomas--7 cases (2.8%). In 10 seminomas (4.1%() we have found syncytiothrophoblastic giant cells. In comparison to other investigations, the number of anaplastic seminomas is very low, but on the other hand the diagnosis Of this tumor is problematic, especially, the differential diagnosis of solid variants of embryonal carcinomas. The most common non-seminomatous tumor in this group is the embryonal carcinoma (16.8%). No polyembryoma and choriocarcinoma were observed, and only 2 yolk-sac-tumors occurred in infants. The occurrence of teratomas was also low, i.e. 15 cases of mature teratoma and 13 cases of immature teratoma. In the group of tumors of more than one histologic type, cases showing embryonal carcinoma and teratoma prevail (83 tumors). In addition to this combination other common tumors of this group (contained structures of seminomas (25 cases), yolk-sac-tumors (22 cases), an choriocarcinomas (19 cases) and embryonal carcinomas and yolk-sac-tumors (13 cases). Altogether, this group comprised 72.8% of the non-seminomatous tumors. Furthermore, the peculiarities of germ cell tumors of childhood are described. In this group the mature teratomas prevail. No seminoma could be registered in infancy. The distribution of our cases among the various types and the subgroups agreed in the main classes with that reported in literature but in special differentiations there are some discrepancies. The problem of classification of germ cell tumors is discussed.

摘要

采用世界卫生组织的命名法,对552例睾丸生殖细胞肿瘤进行了重新分类。分析结果如下:生殖细胞肿瘤在幼儿期(3个月至3岁)出现,在成年期(26 - 35岁)发病率达到高峰,而在老年男性中仅有少数病例。4至13岁之间未发现生殖细胞肿瘤。我们的资料包括245例精原细胞瘤(44.4%)和307例非精原细胞性生殖细胞肿瘤(55.6%)。在单一组织学类型的肿瘤组中,245例精原细胞瘤占主要部分。识别出以下亚组:典型精原细胞瘤——229例(93.5%),精母细胞性精原细胞瘤——9例(3.7%),间变性精原细胞瘤——7例(2.8%)。在10例精原细胞瘤(4.1%)中发现了合体滋养层巨细胞。与其他研究相比,间变性精原细胞瘤的数量非常少,但另一方面,该肿瘤的诊断存在问题,尤其是胚胎癌实体变体的鉴别诊断。该组中最常见的非精原细胞瘤是胚胎癌(16.8%)。未观察到多胚瘤和绒毛膜癌,婴儿中仅出现2例卵黄囊瘤。畸胎瘤的发生率也较低,即成熟畸胎瘤15例,未成熟畸胎瘤13例。在多种组织学类型的肿瘤组中,以胚胎癌和畸胎瘤为主(83例)。除了这种组合外,该组其他常见肿瘤包括含有精原细胞瘤结构的(25例)、卵黄囊瘤(22例)、绒毛膜癌(19例)以及胚胎癌和卵黄囊瘤(13例)。该组总共占非精原细胞瘤的72.8%。此外,还描述了儿童生殖细胞肿瘤的特点。在该组中成熟畸胎瘤占主导。婴儿期未发现精原细胞瘤。我们病例在各种类型和亚组中的分布在主要类别上与文献报道一致,但在特殊分类上存在一些差异。讨论了生殖细胞肿瘤的分类问题。

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