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早期识别胎儿淋巴管瘤的价值。

The value of early recognition of fetal lymphangioma.

作者信息

Farnaghi Soheil, Kothari Alka

机构信息

Redcliffe Hospital Redcliffe Queensland Australia.

出版信息

Australas J Ultrasound Med. 2013 Aug;16(3):147-152. doi: 10.1002/j.2205-0140.2013.tb00103.x. Epub 2015 Dec 31.

DOI:10.1002/j.2205-0140.2013.tb00103.x
PMID:28191189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5029997/
Abstract

: Lymphangiomas are very rare benign tumors of the lymphatic system, appearing as uniseptate or multiseptate cystic masses, which are usually located in the cervical or axillary area. Postnatal outcome depends on the size and location of the lesion. An increasing number of such congenital abnormalities are detected on routine conventional prenatal ultrasonography. Although prenatal evaluation for the prognosis of fetal lymphangioma has been based on two-dimensional ultrasonography, magnetic resonance imaging may help in assessing the extent of a lesion. Isolated lymphangiomas generally have a favourable prognosis and sclerotherapy or surgical resection is effective in most of the cases. : We present two cases of fetal axillary lymphangioma. In the first case, the lymphangioma was diagnosed antenatally, so parents were comprehensively counselled and post natal follow up was organised at a tertiary hospital. The second case remained undiagnosed until birth. This caused significant distress to both the parents and clinicians, especially after a coincident traumatic delivery. : Both these cases emphasise that early diagnosis of fetal lymphangioma is critical and a combination of ultrasonography and magnetic resonance imaging can facilitate detection of lesions which are relatively limited and accessible to therapy in utero. This would also enable clinicians to perform a karyotype and comprehensively consult parents regarding the treatment and delivery options as well as outcome of the pregnancy.

摘要

淋巴管瘤是淋巴系统非常罕见的良性肿瘤,表现为单房或多房囊性肿块,通常位于颈部或腋窝区域。出生后的预后取决于病变的大小和位置。在常规产前超声检查中发现的此类先天性异常的数量越来越多。虽然胎儿淋巴管瘤预后的产前评估一直基于二维超声检查,但磁共振成像可能有助于评估病变范围。孤立性淋巴管瘤通常预后良好,在大多数情况下,硬化治疗或手术切除有效。:我们报告两例胎儿腋窝淋巴管瘤病例。第一例中,淋巴管瘤在产前被诊断出来,因此对父母进行了全面咨询,并在一家三级医院安排了产后随访。第二例直到出生才被诊断出来。这给父母和临床医生都带来了极大的困扰,尤其是在同时发生创伤性分娩之后。:这两例病例都强调,胎儿淋巴管瘤的早期诊断至关重要,超声检查和磁共振成像相结合可以促进对相对局限且在子宫内可进行治疗的病变的检测。这也将使临床医生能够进行核型分析,并就治疗和分娩选择以及妊娠结局与父母进行全面咨询。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/cdc1b1dfbba4/AJUM-16-147-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/48a69c063b49/AJUM-16-147-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/415f6bc622c7/AJUM-16-147-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/951f29c5a519/AJUM-16-147-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/1ec798d41c52/AJUM-16-147-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/158cf2ef62b7/AJUM-16-147-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/cdc1b1dfbba4/AJUM-16-147-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/48a69c063b49/AJUM-16-147-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/415f6bc622c7/AJUM-16-147-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/e6734abff14e/AJUM-16-147-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/951f29c5a519/AJUM-16-147-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a814/5029997/cdc1b1dfbba4/AJUM-16-147-g007.jpg

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本文引用的文献

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Fetal cystic lymphangioma of the neck: a case report.胎儿颈部囊性淋巴管瘤:一例报告
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Congenital fetal lymphangioma causing shoulder dystocia and uterine rupture.先天性胎儿淋巴管瘤导致肩难产和子宫破裂。
Int J Gynaecol Obstet. 2011 Mar;112(3):248. doi: 10.1016/j.ijgo.2010.09.018. Epub 2011 Jan 17.
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罕见先天性淋巴管瘤胎儿心脏评估的价值:来自单一三级中心二十年(1999 - 2020年)的队列研究
J Clin Med. 2022 Feb 16;11(4):1035. doi: 10.3390/jcm11041035.
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