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婴儿伯-韦综合征伴间皮包涵囊肿。

Mesothelial Inclusion Cyst in an Infant with Beckwith-Weidemann Syndrome.

机构信息

Department of Surgery, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, NC, USA.

出版信息

Am Surg. 2023 Aug;89(8):3616-3617. doi: 10.1177/00031348231167408. Epub 2023 Mar 27.

DOI:10.1177/00031348231167408
PMID:36973236
Abstract

Mesothelial inclusion cysts are rare benign tumors not frequently reported in the literature. When reported, they are primarily found in adults. One report from 2006 reports an association with Beckwith-Weideman syndrome, but no other reported cases discuss this correlation. We describe a case of an infant with Beckwith-Weideman syndrome who, in the setting of omphalocele repair, was found to have hepatic cysts with pathology revealing mesothelial inclusion cysts.

摘要

间皮包涵囊肿是罕见的良性肿瘤,在文献中报道较少。当被报道时,它们主要发生在成年人中。2006 年的一份报告报告了与 Beckwith-Weideman 综合征的关联,但没有其他报告的病例讨论这种相关性。我们描述了一例 Beckwith-Weideman 综合征婴儿,在脐膨出修复术中发现肝脏囊肿,病理显示为间皮包涵囊肿。

相似文献

1
Mesothelial Inclusion Cyst in an Infant with Beckwith-Weidemann Syndrome.婴儿伯-韦综合征伴间皮包涵囊肿。
Am Surg. 2023 Aug;89(8):3616-3617. doi: 10.1177/00031348231167408. Epub 2023 Mar 27.
2
Accessory liver lobe with mesothelial inclusion cysts in an omphalocele: a new malformative association.
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Bilateral benign haemorrhagic adrenal cysts in Beckwith-Wiedemann syndrome: case report.
East Afr Med J. 2004 Jan;81(1):59-60. doi: 10.4314/eamj.v81i1.8798.
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Unknown syndrome: radial ray defects, omphalocele, diaphragmatic hernia, and hepatic cyst.不明综合征:桡骨射线缺陷、脐膨出、膈疝和肝囊肿。
J Med Genet. 1990 Jun;27(6):403-4. doi: 10.1136/jmg.27.6.403.
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Adrenal masses associated with Beckwith Wiedemann syndrome in the newborn.新生儿中与贝克威思-维德曼综合征相关的肾上腺肿块。
Afr J Paediatr Surg. 2010 Sep-Dec;7(3):209-10. doi: 10.4103/0189-6725.70431.
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Cystic adrenal masses in the neonate associated with hemihypertrophy and the relation to the Beckwith-Wiedemann syndrome.
J Urol. 1991 Aug;146(2 ( Pt 2)):580-2. doi: 10.1016/s0022-5347(17)37861-8.
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