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偶然发现的无症状脾错构瘤误诊为动脉瘤:一例报告。

Incidentally discovered asymptomatic splenic hamartoma misdiagnosed as an aneurysm: A case report.

作者信息

Cao Xue-Feng, Yang Li-Peng, Fan Song-Song, Wei Qiang, Lin Xu-Tao, Zhang Xing-Yuan, Kong Ling-Qun

机构信息

Department of Hepatobiliary Surgery, Binzhou Medical University Hospital, Binzhou 256603, Shandong Province, China.

Department of Hepatobiliary Surgery and Clinical Nutrition Center, Binzhou Medical University Hospital, Binzhou 256600, Shandong Province, China.

出版信息

World J Clin Cases. 2021 Aug 26;9(24):7231-7236. doi: 10.12998/wjcc.v9.i24.7231.

DOI:10.12998/wjcc.v9.i24.7231
PMID:34540983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8409209/
Abstract

BACKGROUND

Splenic hamartoma (SH) is a rare, benign vascular proliferation that is often found incidentally. It may be misdiagnosed as a splenic aneurysm or splenic malignancy.

CASE SUMMARY

A 21-year-old male patient was admitted to our hospital with a complaint of an incidentally discovered asymptomatic splenic space-occupying lesion for 2 wk. Abdominal computed tomography (CT) scan showed a circular low-density shadow in the hilum of the spleen. Contrast-enhanced CT revealed an aneurysm located in the hilum of the spleen before operation. Laparoscopic splenectomy was performed and postoperative pathology revealed the presence of SH.

CONCLUSION

Imaging studies are insufficient for the differential diagnosis of SH from other diseases, and laparoscopic splenectomy is a less invasive procedure and useful for the diagnostic purpose as well.

摘要

背景

脾错构瘤(SH)是一种罕见的良性血管增殖性病变,常为偶然发现。它可能被误诊为脾动脉瘤或脾恶性肿瘤。

病例摘要

一名21岁男性患者因偶然发现无症状脾占位性病变2周入院。腹部计算机断层扫描(CT)显示脾门处有一个圆形低密度影。术前增强CT显示脾门处有一个动脉瘤。行腹腔镜脾切除术,术后病理显示为脾错构瘤。

结论

影像学检查不足以将脾错构瘤与其他疾病进行鉴别诊断,腹腔镜脾切除术是一种侵入性较小的手术,对诊断也有帮助。

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本文引用的文献

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Laparoscopic splenectomy for isolated splenic sarcoidosis: A case report.腹腔镜脾切除术治疗孤立性脾结节病:一例报告
Int J Surg Case Rep. 2019;60:79-81. doi: 10.1016/j.ijscr.2019.04.031. Epub 2019 Apr 19.
2
A giant splenic hamartoma associated with hematologic disorders: A case report.一例与血液系统疾病相关的巨大脾脏错构瘤:病例报告
Ann Med Surg (Lond). 2018 Nov 16;36:199-202. doi: 10.1016/j.amsu.2018.11.003. eCollection 2018 Dec.
3
First case of laparoscopic partial splenectomy in a child with hamartoma: Case report and review of the literature.
小儿错构瘤行腹腔镜脾部分切除术首例:病例报告及文献复习
Int J Surg Case Rep. 2018;53:140-143. doi: 10.1016/j.ijscr.2018.09.018. Epub 2018 Sep 17.
4
Inflammatory pseudotumor-like follicular dendritic cell tumor of the spleen.脾脏炎性假瘤样滤泡树突状细胞肿瘤
Turk J Gastroenterol. 2018 Jan;29(1):128-130. doi: 10.5152/tjg.2018.17220.
5
Splenic hamartoma with bizarre stromal cells: a case report and literature review.伴有奇异间质细胞的脾错构瘤:1例报告及文献复习
Diagn Pathol. 2018 Jan 22;13(1):8. doi: 10.1186/s13000-018-0687-y.
6
Splenic hamartoma is a rare cause of abdominal pain: Case report and literature review.脾错构瘤是腹痛的罕见病因:病例报告及文献综述
Turk J Surg. 2015 Jul 14;33(4):294-295. doi: 10.5152/UCD.2015.3048. eCollection 2017.
7
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Int J Surg Case Rep. 2017;39:172-175. doi: 10.1016/j.ijscr.2017.08.005. Epub 2017 Aug 10.
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Negative F-FDG PET and positive CT and MRI findings in multifocal splenic hamartoma.多灶性脾错构瘤的F-FDG PET表现为阴性,CT和MRI表现为阳性。
Hell J Nucl Med. 2017 May-Aug;20(2):182-183. doi: 10.1967/s002449910563. Epub 2017 Jul 12.
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Pathol Int. 2015 May;65(5):254-8. doi: 10.1111/pin.12277. Epub 2015 Mar 2.
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