Gondos B, Egli C A, Rosenthal S M, Grumbach M M
Arch Pathol Lab Med. 1985 Nov;109(11):990-5.
A recently described form of male sexual precocity characterized by active Leydig cell differentiation and premature onset of spermatogenesis in the absence of pituitary gonadotropin stimulation has been termed familial testotoxicosis. The clinical and endocrine findings in the condition are consistent with an inherited intratesticular defect rather than central or true precocious puberty. In this report, testicular changes in biopsy specimens from a series of affected patients are presented. In all of the cases, Leydig cells demonstrated nuclear and cytoplasmic features characteristic of fully differentiated steroidogenic cells. Reinke crystals were absent. Germ cells at all stages of spermatogenesis were present, but there was evident disorganization of maturation. Spermatids exhibited a variety of structural abnormalities. Sertoli cells were characterized by complex cytoplasmic differentiation, Charcot-Böttcher crystals, and tight junction formation. The morphologic changes indicate premature differentiation of all of the major testicular cell types and are consistent with a distinctive type of intratesticular abnormality.
最近描述的一种男性性早熟形式,其特征为在无垂体促性腺激素刺激的情况下,睾丸间质细胞活跃分化且精子发生过早开始,这种情况被称为家族性睾丸中毒症。该病症的临床和内分泌表现与遗传性睾丸内缺陷相符,而非中枢性或真性性早熟。在本报告中,展示了一系列受影响患者活检标本中的睾丸变化。在所有病例中,睾丸间质细胞呈现出完全分化的类固醇生成细胞的核和胞质特征。无雷氏晶体。存在精子发生各阶段的生殖细胞,但成熟过程明显紊乱。精子细胞表现出多种结构异常。支持细胞的特征为复杂的胞质分化、夏科 - 博彻晶体和紧密连接形成。形态学变化表明所有主要睾丸细胞类型均过早分化,与一种独特类型的睾丸内异常相符。