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Mature and immature solid teratomas involving uterine corpus cervix and ovary

机译:成熟和不成熟的实体畸胎瘤累及子宫体子宫颈和卵巢

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摘要

Extragonadal teratomas are rare, and localization in the endometrium and cervix is exceptional, with only up to 10 case reports documented so far in the English literature. We present here the case of a 46-year-old patient who presented with simultaneous immature teratoma in the endometrium and mature teratomas in the ovary in association with gliomatosis peritonei but with no evidence of gestational origin; she subsequently developed multiple solid mature teratomas in the cervix and parauterine tissue. No other similar cases have been previously reported to our knowledge. There are many similarities between the patient’s pattern of recurrence and “growing teratoma syndrome (GTS).” Although the patient was not treated with chemotherapy after her first presentation and this case does not meet formal criteria for GTS, we believe that the pattern and histology of recurrences in this case represent a variant of GTS. Considering that the initial presentation in this case was endometrial and ovarian makes the occurrence of GTS-like syndrome even more unique.
机译:性腺外畸胎瘤很罕见,在子宫内膜和子宫颈中的定位异常,英语文献中迄今仅记录了10例病例报告。我们在这里介绍了一个46岁的患者,该患者同时出现子宫内膜未成熟畸胎瘤和卵巢成熟畸胎瘤并伴有腹膜性胶质瘤病,但没有妊娠起源的证据。她随后在子宫颈和子宫旁组织中形成了多个实体成熟的畸胎瘤。据我们所知,以前没有其他类似案例的报道。病人的复发方式与“不断增长的畸胎瘤综合征(GTS)”之间有许多相似之处。尽管该患者首次就诊后未接受化学疗法治疗,并且该病例不符合GTS的正式标准,但我们认为该病例的复发方式和组织学是GTS的一种变异。考虑到这种情况的最初表现是子宫内膜和卵巢,使得GTS样综合征的发生更加独特。

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