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Preoperative multimodal ultrasonic imaging in a case of Peutz-Jeghers syndrome complicated by atypical lobular endocervical glandular hyperplasia: a case report and literature review.

Authors :
Yang, Liwen
Duan, Duan
Xiong, Ying
Liu, Tianjiao
Zhao, Lijun
Lai, Fan
Gu, Dingxian
Zhou, Liuying
Source :
Hereditary Cancer in Clinical Practice. 2/28/2024, Vol. 22 Issue 1, p1-13. 13p.
Publication Year :
2024

Abstract

Background: Peutz-Jeghers syndrome (PJS), an autosomal dominant multiple cancerous disorder, is clinically characterized by mucocutaneous macules and multiple gastrointestinal hamartomatous polyps. Gastric-type endocervical adenocarcinoma (G-EAC), a special subtype of cervical adenocarcinoma with non-specific symptoms and signs, is known to occur in approximately 11% of female patients with PJS. Case presentation: Here, we report a case of PJS in a 24-year-old female with multiple mucocutaneous black macules who complained of vaginal discharge and menorrhagia. Moreover, we first described the multimodal ultrasonographical manifestations of PJS-correlated G-EAC. The three-dimensional reconstructed view of G-EAC on 3D realisticVue exhibited a distinctive "cosmos pattern" resembling features on magnetic resonance imaging, and the contrast-enhanced ultrasound displayed a "quick-up and slow-down" pattern of the solid components inside the mixed cervical echoes. We reported the multimodal ultrasonographical characteristics of a case of PJS-related G-EAC, as well as reviewed PJS-related literature and medical imaging features and clinical characteristics of G-EAC to provide insight into the feasibility and potential of utilizing multimodal ultrasonography for the diagnosis of G-EAC. Conclusions: Multimodal ultrasound can visualize morphological features, solid components inside, and blood supplies of the G-EAC lesion and distinguish the G-EAC lesion from normal adjacent tissues. This facilitates preoperative diagnosis and staging of PJS-related G-EAC, thereby aiding subsequent health and reproductive management for patients with PJS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17312302
Volume :
22
Issue :
1
Database :
Academic Search Index
Journal :
Hereditary Cancer in Clinical Practice
Publication Type :
Academic Journal
Accession number :
175754796
Full Text :
https://doi.org/10.1186/s13053-024-00275-7