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本文引用的文献

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Management of prenatally diagnosed abdominal lymphatic malformations.产前诊断的腹部淋巴管畸形的管理
Eur J Pediatr Surg. 2010 Sep;20(5):302-6. doi: 10.1055/s-0030-1254149. Epub 2010 Jun 24.
2
D2-40 immunohistochemistry--so far!D2-40免疫组织化学——目前为止!
Adv Anat Pathol. 2009 Jan;16(1):62-4. doi: 10.1097/PAP.0b013e3181915e94.
3
Retroperitoneal lymphangioma: an unusual location and presentation.腹膜后淋巴管瘤:一个不寻常的部位及表现。
J Pediatr Surg. 2006 Mar;41(3):603-5. doi: 10.1016/j.jpedsurg.2005.11.057.
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Cystic lymphangioma of the right adrenal gland.右肾上腺囊性淋巴管瘤。
Pathol Oncol Res. 2005;11(4):242-4. doi: 10.1007/BF02893858. Epub 2005 Dec 31.
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Further experience with OK-432 for lymphangiomas.
Pediatr Surg Int. 2005 Dec;21(12):969-72. doi: 10.1007/s00383-005-1564-9. Epub 2005 Oct 25.
6
Intra-abdominal and retroperitoneal lymphangiomas in pediatric and adult patients.小儿及成人患者的腹腔内和腹膜后淋巴管瘤
World J Surg. 2005 Jul;29(7):837-40. doi: 10.1007/s00268-005-7794-0.
7
Retroperitoneal cystic masses: CT, clinical, and pathologic findings and literature review.腹膜后囊性肿块:CT、临床及病理表现并文献复习
Radiographics. 2004 Sep-Oct;24(5):1353-65. doi: 10.1148/rg.245045017.
8
Cystic adrenal lymphangioma.肾上腺囊性淋巴管瘤
Arch Pathol Lab Med. 2004 Jun;128(6):713-4. doi: 10.5858/2004-128-713-CAL.
9
[Mesenteric cysts].[肠系膜囊肿]
Acta Med Croatica. 2002;56(3):119-24.
10
Abdominal cystic lymphangiomas in children: presurgical evaluation with imaging.儿童腹部囊性淋巴管瘤:术前影像学评估
Eur J Pediatr Surg. 2002 Feb;12(1):13-8. doi: 10.1055/s-2002-25090.

儿童腹膜后、肠系膜及网膜囊肿的手术经验。

The surgical experience for retroperitoneal, mesenteric and omental cyst in children.

作者信息

Nam So Hyun, Kim Dae Yeon, Kim Seong Chul, Kim In Koo

机构信息

Department of Pediatric Surgery, Inje University Haeundae Paik Hospital, Busan, Korea.

出版信息

J Korean Surg Soc. 2012 Aug;83(2):102-6. doi: 10.4174/jkss.2012.83.2.102. Epub 2012 Jul 25.

DOI:10.4174/jkss.2012.83.2.102
PMID:22880185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3412181/
Abstract

PURPOSE

Intra-abdominal cystic masses originating from the retroperitoneum, mesentery or omentum are very rare and mostly benign tumors, but sometimes present as a complicated cyst encasing the major organs.

METHODS

We analyzed the clinical findings, histologic diagnosis, and surgical outcomes in children who underwent operation for retroperitoneal, omental, and mesenteric cyst from 1998 to 2010, retrospectively.

RESULTS

Twenty-three patients (male, 12; female, 11) underwent the operation at a median age of 46 months (range, 9 days to 16 years). Among them, 17 cysts presented one or two symptoms such as abdominal mass, abdominal pain or abdominal distension. The median duration of symptoms was 7 days (range, 1 day to 365 days). Five were detected prenatally. Ten cysts were found in retroperitoneum, 8 in the omentum and 5 in the mesentery. The median diameter was 13 cm (range, 3 to 30 cm). Twenty cysts were completely removed. Five mesenteric cysts required bowel resection and anastomosis. Three of retroperitoneal cysts were impossible to complete excise because of location and extensiveness. Pathologically, 20 cysts were lymphangioma and 3 were pseudocyst. The morbidity was one of adhesive ileus and the mortality was one who had extensive retroperitoneal cyst with mesenteric cyst. He died from sepsis. During follow-up period, there was no recurrence.

CONCLUSION

Preoperative diagnosis and localization for these cysts are very difficult. Complete excision was possible in almost all cases despite the size, bringing a favorable outcome. The possibility of this disease entity should be considered as the cause of acute abdomen.

摘要

目的

起源于腹膜后、肠系膜或网膜的腹腔内囊性肿块非常罕见,大多为良性肿瘤,但有时表现为包裹主要器官的复杂囊肿。

方法

我们回顾性分析了1998年至2010年接受腹膜后、网膜和肠系膜囊肿手术的儿童的临床发现、组织学诊断和手术结果。

结果

23例患者(男12例,女11例)接受了手术,中位年龄为46个月(范围9天至16岁)。其中,17个囊肿出现一种或两种症状,如腹部肿块、腹痛或腹胀。症状的中位持续时间为7天(范围1天至365天)。5例在产前被检测到。10个囊肿位于腹膜后,8个在网膜,5个在肠系膜。中位直径为13厘米(范围3至30厘米)。20个囊肿被完全切除。5个肠系膜囊肿需要进行肠切除和吻合术。3个腹膜后囊肿由于位置和范围无法完全切除。病理检查,20个囊肿为淋巴管瘤,3个为假性囊肿。发病率为粘连性肠梗阻1例,死亡率为1例,该患者患有广泛的腹膜后囊肿并伴有肠系膜囊肿,死于败血症。随访期间无复发。

结论

这些囊肿的术前诊断和定位非常困难。尽管囊肿大小不一,但几乎所有病例都能完全切除,预后良好。应考虑这种疾病实体作为急腹症的病因。