1岁以下儿童颗粒细胞瘤伴假性性早熟。2例)。

Chirurgie pediatrique Pub Date : 1990-01-01
M Bonnevalle, F Mazingue, B Nelken, P Vaast, M Lecomte-Houcke, P Debeugny
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引用次数: 0

摘要

本文报道两例同性早熟与颗粒细胞瘤有关的2例女孩,年龄分别为6个月和9个月。在这两个病例的临床和生物学迹象发现高雌激素血症,但在一个,急性迹象肿瘤破裂是第一症状。组织学上发现两种典型亚型:大滤泡型(“成年”型)和“幼年”型。这两个孩子在随访12个月和18个月后没有任何复发迹象。在这样的年轻女孩中发生颗粒细胞瘤似乎是极其罕见的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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[Precocious pseudo-puberty in granulosa cell tumor in children less than 1 year old. 2 cases].

Two cases of isosexual precocity in relation to granulosa cell tumor in 2 girls aged 6 and 9 months respectively are described. In the two cases clinical and biological signs of hyperoestrogenemia were found but in one, acute signs of tumoral rupture were the first symptom. Histologically, the two classical subtypes were found: macrofollicular ("adult" type) and "juvenile". These two children are alive without any sign of recurrence with a follow up of 12 and 18 months. The occurrence of granulosa cell tumors in such young girls seems extremely rare.

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