Suppr超能文献

产前检测巨大淋巴管瘤从侧腹至下肢的快速进展性变化。

Prenatal Detection of Rapid Progressive Changes in Massive Lymphangioma from Flank to the Lower Extremity.

作者信息

Pongsatha Saipin, Jatavan Phudit, Hantrakun Panisa, Tongsong Theera

机构信息

Department of Obstetrics and Gynecology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Diagnostics (Basel). 2023 Jun 21;13(13):2130. doi: 10.3390/diagnostics13132130.

Abstract

Lymphangioma is a congenital anomaly in which abnormal lymphatic drainages localize to form a benign mass, but it has the tendency to grow in size and the potential to infiltrate surrounding structures, causing devastating effects and leading to severe morbidity. The most common site of lymphangioma is the neck region (cystic hygroma colli), whereas lymphangioma in the lower limbs is very rare, accounting for only 2% of cases. Accordingly, the prenatal diagnosis of lymphangioma of the lower limbs has been scarcely reported. This study describes two cases of lymphangioma of the lower limbs, focusing on unique sonographic features and the natural course of rapidly progressive changes, which is different from nuchal lymphangioma. Based on previous isolated case reports together with our two cases, lymphangioma of the lower limbs usually develops in the second trimester, tends to have rapidly progressive changes, and is unlikely to be associated with aneuploidy and structural anomalies. Diagnoses can be made by using sonographic findings pertaining to the subcutaneous complex and multi-septate anechoic cystic lesions in the lower limbs, the latter of which can infiltrate visceral structures. Prenatal detection can be helpful in laying the groundwork for providing counseling to the parents and the planning of management strategies, i.e., opting to terminate the pregnancy, revising delivery plans, and looking towards the postnatal management of the infant.

摘要

淋巴管瘤是一种先天性异常,其中异常的淋巴引流定位形成良性肿块,但它有体积增大的趋势,并有可能浸润周围结构,造成破坏性影响并导致严重的发病情况。淋巴管瘤最常见的部位是颈部(颈部囊状水瘤),而下肢淋巴管瘤非常罕见,仅占病例的2%。因此,下肢淋巴管瘤的产前诊断鲜有报道。本研究描述了两例下肢淋巴管瘤病例,重点关注独特的超声特征以及快速进展变化的自然病程,这与颈部淋巴管瘤不同。基于之前的孤立病例报告以及我们的两例病例,下肢淋巴管瘤通常在孕中期发病,倾向于快速进展变化,并且不太可能与非整倍体和结构异常相关。通过使用与下肢皮下复合性多分隔无回声囊性病变相关的超声检查结果可以做出诊断,后者可浸润内脏结构。产前检测有助于为向父母提供咨询以及制定管理策略奠定基础,即选择终止妊娠、修改分娩计划以及考虑婴儿的产后管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0209/10340443/1311d0455296/diagnostics-13-02130-g001a.jpg

相似文献

1
Prenatal Detection of Rapid Progressive Changes in Massive Lymphangioma from Flank to the Lower Extremity.
Diagnostics (Basel). 2023 Jun 21;13(13):2130. doi: 10.3390/diagnostics13132130.
2
Prenatal diagnosis of cystic hygroma cases in a tertiary centre and retrospective analysis of pregnancy results.
J Obstet Gynaecol. 2022 Oct;42(7):2899-2904. doi: 10.1080/01443615.2022.2112023. Epub 2022 Aug 25.
5
Natural Course of Fetal Axillary Lymphangioma Based on Prenatal Ultrasound Studies.
J Ultrasound Med. 2018 May;37(5):1273-1281. doi: 10.1002/jum.14473. Epub 2017 Nov 9.
6
Cavernous lymphangioma of the face and neck: prenatal diagnosis by three-dimensional ultrasound.
Ultrasound Obstet Gynecol. 2005 Sep;26(3):300-2. doi: 10.1002/uog.1972.
8
Prenatal sonographic documentation of cystic hygroma regression in Noonan syndrome.
Am J Med Genet. 1991 Jun 15;39(4):461-5. doi: 10.1002/ajmg.1320390418.
9
Prenatal diagnosis of fetal chest lymphangioma.
J Ultrasound Med. 2006 Nov;25(11):1437-40. doi: 10.7863/jum.2006.25.11.1437.
10
First trimester cystic hygroma colli: Retrospective analysis in a tertiary center.
Eur J Obstet Gynecol Reprod Biol. 2018 Dec;231:60-64. doi: 10.1016/j.ejogrb.2018.10.019. Epub 2018 Oct 9.

引用本文的文献

1
When Giant Lymphangioma Meets Hydrops Fetalis: An Uncommon Case Report of Lower Extremity Involvement.
Matern Fetal Med. 2024 Oct 11;6(4):253-256. doi: 10.1097/FM9.0000000000000249. eCollection 2024 Oct.
2
Interesting Images in Obstetrics and Gynecology.
Diagnostics (Basel). 2024 Jul 18;14(14):1558. doi: 10.3390/diagnostics14141558.

本文引用的文献

1
Treatment and prognosis of fetal lymphangioma.
Eur J Obstet Gynecol Reprod Biol. 2018 Dec;231:274-279. doi: 10.1016/j.ejogrb.2018.10.031. Epub 2018 Oct 15.
2
Fetal Lymphangioma: Prenatal diagnosis on ultrasound, treatment, and prognosis.
Eur J Obstet Gynecol Reprod Biol. 2018 Dec;231:268-273. doi: 10.1016/j.ejogrb.2018.10.018. Epub 2018 Oct 9.
3
Natural Course of Fetal Axillary Lymphangioma Based on Prenatal Ultrasound Studies.
J Ultrasound Med. 2018 May;37(5):1273-1281. doi: 10.1002/jum.14473. Epub 2017 Nov 9.
4
Lymphangioma involving the foetal lower limb, a rare condition diagnosed on prenatal ultrasound.
J Clin Diagn Res. 2014 Jul;8(7):OD10-1. doi: 10.7860/JCDR/2014/6937.4581. Epub 2014 Jul 20.
5
Extensive fetal abdominopelvic lymphangioma.
Ultrasound Q. 2008 Jun;24(2):115-9. doi: 10.1097/RUQ.0b013e31817b6297.
6
Fetal abdomino-perineal lymphangioma: differential diagnosis and management.
Prenat Diagn. 2006 Aug;26(8):692-5. doi: 10.1002/pd.1481.
7
Three-dimensional ultrasound of a massive fetal lymphangioma involving the lower extremity.
Ultrasound Obstet Gynecol. 2003 Nov;22(5):547-9. doi: 10.1002/uog.915.
8
Prenatal diagnosis of abdominal lymphangioma.
Ultrasound Obstet Gynecol. 2002 Aug;20(2):205-6. doi: 10.1046/j.1469-0705.2002.00750_2.x.
9
Prognosis of fetuses with a cystic hygroma.
Prenat Diagn. 1991 Jun;11(6):349-55. doi: 10.1002/pd.1970110603.
10
Prenatal sonographic findings of massive lower extremity lymphangioma.
Am J Perinatol. 1992 Mar;9(2):127-9. doi: 10.1055/s-2007-994685.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验