Diagnosis and Management of an Adenomatoid Uterine Tumor: Ultrasound, Magnetic Resonance Imaging, Surgical Appearance, and Pathology Correlation.

Q2 Biochemistry, Genetics and Molecular Biology
BioResearch Open Access Pub Date : 2018-10-26 eCollection Date: 2018-01-01 DOI:10.1089/biores.2018.0023
Jennie Orlando, Cornelia deRiese, Eric Blackwell, Suzanne Graham, Jennifer Phy
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引用次数: 3

Abstract

Adenomatoid uterine tumors are rare, and their appearance on medical imaging modalities is not well established. We present a case of an adenomatoid uterine tumor reviewing a unique sonographic presentation, magnetic resonance imaging (MRI), gross surgical appearance of the tumor, and microscopic pathology images. A 29-year-old gravida 0 Caucasian woman presented with dysmenorrhea, menorrhagia, and desire to conceive. Transvaginal ultrasound revealed a 2.7 cm round, well-circumscribed posterior intramural uterine mass. The mass was hyperechoic centrally with a thin hypoechoic rim. Color Doppler imaging revealed a prominent vascular rim around the periphery of the mass as well as central vascularity not typical for a leiomyoma. MRI, with and without intravenous gadolinium, was obtained showing a 2.7 cm posterior fundal mildly enhancing uterine mass suggestive of leiomyoma. The mass had a heterogeneous signal pattern on T2-weighted images, and no fat component was noted within the mass. Repeat transvaginal ultrasound showed interval growth of the mass to 3.5 cm with a lipomatous appearance. Adenomatoid uterine tumors are rare and may be mistaken for uterine leiomyomata. Unique features include sonographic appearance of central hyperechogenicity with a hypoechoic rim and prominent peripheral and central vascularity in conjunction with MRI revealing a heterogeneous signal pattern on T2-weighted images without fat component. Gross surgical appearance reveals a nondiscrete capsule and secretion of mucoid material when the mass is exposed. We present a case of adenomatoid tumor providing sonographic, MRI, surgical, and pathological correlation. The patient subsequently conceived spontaneously and delivered at term by cesarean section. The patient underwent a preoperative evaluation with complete blood count, comprehensive metabolic panel, blood type with antibody screen, and pregnancy test. She underwent laparoscopic excision with robotic assistance for removal of the tumor. Grossly, the uterine mass had a very soft consistency atypical for a uterine leiomyoma making dissection more challenging. During dissection the mass diffusely secreted a mucoid material although the capsule was not disrupted. The lesion was excised intact and was removed from the peritoneal cavity in an endocatch bag without internal morcellation. Microscopic examination revealed an adenomatoid tumor.

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子宫腺瘤样肿瘤的诊断和治疗:超声、磁共振成像、手术表现和病理相关性。
子宫腺瘤样肿瘤是罕见的,其外观的医学影像模式尚未很好地建立。我们报告一个子宫腺瘤样肿瘤的病例,回顾其独特的超声表现、磁共振成像(MRI)、肿瘤的大体手术外观和显微病理图像。一名29岁的白种人孕妇,以痛经、月经过多和渴望怀孕为主诉。经阴道超声显示一个2.7厘米的圆形子宫壁内肿块。肿块中央高回声,边缘薄低回声。彩色多普勒成像显示肿块周围有明显的血管边缘和中心血管,这不是平滑肌瘤的典型特征。MRI,不论有无静脉注射钆,显示子宫后部2.7 cm轻度增强肿块,提示子宫平滑肌瘤。肿块在t2加权图像上呈非均匀信号模式,肿块内未见脂肪成分。重复经阴道超声显示肿块间隔生长至3.5厘米,呈脂肪瘤样。子宫腺瘤样肿瘤罕见,常被误认为子宫平滑肌瘤。独特的特征包括超声表现为中央高回声,边缘低回声,突出的外周和中央血管,同时MRI在t2加权图像上显示不均匀的信号模式,没有脂肪成分。大体手术外观显示一个不离散的囊和粘液物质的分泌时,肿块暴露。我们报告一例腺瘤样肿瘤,提供超声,MRI,手术和病理的相关性。患者随后自然受孕,经剖宫产足月分娩。术前对患者进行全血细胞计数、综合代谢检查、血型抗体筛查和妊娠试验。她在机器人的协助下接受了腹腔镜手术切除肿瘤。肉眼可见,子宫肿块具有非常柔软的稠度,这是非典型的子宫平滑肌瘤,使剥离更具挑战性。在解剖过程中,肿块弥漫性分泌粘液样物质,尽管被囊未被破坏。病变被完整切除,并在没有内部碎裂的情况下从腹膜腔内取出。镜检显示为腺瘤样肿瘤。
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来源期刊
BioResearch Open Access
BioResearch Open Access Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
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1
期刊介绍: BioResearch Open Access is a high-quality open access journal providing peer-reviewed research on a broad range of scientific topics, including molecular and cellular biology, tissue engineering, regenerative medicine, stem cells, gene therapy, systems biology, genetics, virology, and neuroscience. The Journal publishes basic science and translational research in the form of original research articles, comprehensive review articles, mini-reviews, rapid communications, brief reports, technology reports, hypothesis articles, perspectives, and letters to the editor.
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