卵巢纯性亮德氏细胞瘤:一名孕妇罕见的罕见病例。

IF 2.4 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Future Science OA Pub Date : 2024-12-31 Epub Date: 2024-11-21 DOI:10.1080/20565623.2024.2424144
Anwar Rjoop, Alia Almohtaseb, Daoud O Al Aruri, Dina Hyari, Mohammad Abu Shugaer
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引用次数: 0

摘要

目的:莱狄格细胞瘤(LCT)是一种罕见的肿瘤,在所有卵巢肿瘤中占比不到 0.1%。这种肿瘤通常表现为雄激素水平过高的症状和体征。诊断需要结合病史、实验室检查结果、影像学技术和组织病理学检查结果:本病例是一名 35 岁的孕 5 期 3+1 孕妇,在剖宫产手术中意外发现单侧卵巢囊性肿块。囊肿最大尺寸为 9 厘米。在娩出一名存活的男婴后,她接受了左侧卵巢切除术。形态学和免疫分型结果均与纯性莱迪格细胞肿瘤一致:结论:Leydig 细胞肿瘤并不常见,通常表现为雄激素过多。结论:Leydig 细胞肿瘤并不常见,通常表现为雄激素过高,其表现可呈多态性,从迅速出现男性化到无症状不等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pure Leydig cell tumor of the ovary: a rare presentation of a rare entity in a pregnant patient.

Aim: Leydig cell tumors (LCT) are rare neoplasms that represent less than 0.1% of all ovarian tumors. This tumor usually presents with signs and symptoms of excess androgen levels. Diagnosis is made based on a combination of history, laboratory findings, imaging techniques and histopathological findings.Case: We present the case of a 35-year-old gravida five para 3+1 pregnant woman with a unilateral ovarian cystic mass that was discovered incidentally during a cesarean section. The cyst measured 9 cm in its maximum dimension. A left oophorectomy was performed after the delivery of an alive male baby. Morphological and immunophenotypic findings were consistent with those of a pure Leydig cell tumor.Conclusion: Leydig cell tumors are uncommon and usually present with hyperandrogenism. The presentation could be polymorphic, ranging from the rapid onset of virilization to being asymptomatic.

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来源期刊
Future Science OA
Future Science OA MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
5.00
自引率
4.00%
发文量
48
审稿时长
13 weeks
期刊介绍: Future Science OA is an online, open access, peer-reviewed title from the Future Science Group. The journal covers research and discussion related to advances in biotechnology, medicine and health. The journal embraces the importance of publishing all good-quality research with the potential to further the progress of research in these fields. All original research articles will be considered that are within the journal''s scope, and have been conducted with scientific rigour and research integrity. The journal also features review articles, editorials and perspectives, providing readers with a leading source of commentary and analysis. Submissions of the following article types will be considered: -Research articles -Preliminary communications -Short communications -Methodologies -Trial design articles -Trial results (including early-phase and negative studies) -Reviews -Perspectives -Commentaries
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