胎儿颌面畸胎瘤的产前超声诊断:两例报告。

IF 2.6 Q3 ONCOLOGY World journal of clinical oncology Pub Date : 2024-09-24 DOI:10.5306/wjco.v15.i9.1245
Chuan-Fen Gao, Pei Zhou, Chen Zhang
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引用次数: 0

摘要

背景:面部畸胎瘤是一种罕见的良性肿瘤,约占畸胎瘤总数的 1.6%,可通过产前超声(US)诊断。本报告旨在描述我们在妊娠后三个月通过产前超声诊断胎儿面部畸胎瘤的经验,为临床诊断胎儿颌面部畸胎瘤提供参考。病例摘要:我们介绍了两例在我科妊娠后三个月超声检查发现胎儿面部异常的患者。病例 1 是一名 31 岁的 G3 P1 + 1 女性患者,其超声检查发现胎儿面部有 32 mm × 20 mm × 31 mm 的异质回声,大部分位于口腔外并充填口腔根部。病例 2 是一名 29 岁的 G1P0 女性,胎儿头颈部超声显示一囊实性回声肿块,大小为 42 mm × 33 mm × 44 mm,病变上缘达上腭并充满口腔。病变的轮廓通过三维(3D)超声成像得以显现。两名患者均决定放弃治疗。引产后对病灶进行活检,诊断为颌面畸胎瘤:结论:胎儿颌面畸胎瘤可在孕早期通过超声波诊断出来,从而让父母加快做出治疗决定。
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Prenatal ultrasound diagnosis of fetal maxillofacial teratoma: Two case reports.

Background: Facial teratoma is a rare benign tumor that accounts for about 1.6% of all teratomas and can be diagnosed by prenatal ultrasound (US). The purpose of this report was to describe our experience with the diagnosis of fetal facial teratoma by prenatal US at second trimester to provide a reference for clinical diagnosis of fetal maxillofacial teratoma.

Case summary: We present two cases of patients with abnormal fetal facial findings on US at second trimester of pregnancy in our department. Case 1 was a 31-year-old G3 P1 + 1 female, with US revealing a heterogeneous echogenicity of 32 mm × 20 mm × 31 mm on the fetal face, most of it located outside the oral cavity and filling the root of the oral cavity. Case 2 was a 29-year-old G1P0 female, with fetal head and neck US revealing a cystic-solid echo mass measuring 42 mm × 33 mm × 44 mm, the upper edge of the lesion reaching the palate and filling the oral cavity. The contours of the lesions were visualized using three-dimensional (3D) US imaging. Both patients decided to give up treatment. Biopsies of the lesions were performed after induction of labor, and diagnosed as maxillofacial teratoma.

Conclusion: Fetal maxillofacial teratomas can be diagnosed by US in early pregnancy, allowing parents to expedite treatment decisions.

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期刊介绍: The WJCO is a high-quality, peer reviewed, open-access journal. The primary task of WJCO is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of oncology. In order to promote productive academic communication, the peer review process for the WJCO is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJCO are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in oncology. Scope: Art of Oncology, Biology of Neoplasia, Breast Cancer, Cancer Prevention and Control, Cancer-Related Complications, Diagnosis in Oncology, Gastrointestinal Cancer, Genetic Testing For Cancer, Gynecologic Cancer, Head and Neck Cancer, Hematologic Malignancy, Lung Cancer, Melanoma, Molecular Oncology, Neurooncology, Palliative and Supportive Care, Pediatric Oncology, Surgical Oncology, Translational Oncology, and Urologic Oncology.
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