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布加综合征病例:在结核病流行国家中类似腹部结核的谜团——一例病例报告

Case of Budd-Chiari syndrome, an enigma as abdominal tuberculosis in a tubercular endemic country: A case report.

作者信息

Shrestha Riya, Karki Saurab, Timilsina Bibek, Sherpa Tenzin Norphel, Sapkota Suhail, Dhakal Binaya, Kadel Bijan

机构信息

Nepal Medical College, Kathmandu, Nepal.

Military Hospital, Sunsari, Nepal.

出版信息

Ann Med Surg (Lond). 2022 Sep 7;82:104607. doi: 10.1016/j.amsu.2022.104607. eCollection 2022 Oct.

DOI:10.1016/j.amsu.2022.104607
PMID:36268394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9577515/
Abstract

INTRODUCTION AND IMPORTANCE

Bud-Chiari syndrome is an uncommon disease due to obstruction of hepatic venous outflow. Clinical manifestations range from asymptomatic cases to those requiring liver transplants. The study highlights the importance of diagnosing a case of Budd-Chiari syndrome which has been suspected with abdominal tuberculosis where anti-tubercular drugs may themselves damage the liver.

CASE PRESENTATION

Herein we report a case of 18 years old female presenting with upper abdominal pain along with recurrent abdominal distention, jaundice, and deranged liver function. Also, adenosine deaminase level was raised in both pleural and peritoneal fluids, hence, anti-tubercular treatment was started but could not be continued as she developed adverse reactions to these drugs. CT scan later revealed features suggestive of Budd-Chiari syndrome. Initially, she was managed with balloon angioplasty, but her condition worsened ultimately requiring a liver transplant.

CLINICAL DISCUSSION

Budd Chiari syndrome can present with subtle presentation and since abdominal tuberculosis is very non-specific, the two conditions can be very confusing, particularly in the tubercular endemic region. Detailed clinical assessment along with proper investigations and imaging should be performed for early recognition as both conditions are associated with high morbidity and mortality if not treated timely.

CONCLUSION

The necessity of careful investigation and consideration of Budd-Chiari syndrome as an important cause of ascites with jaundice and deranged liver function in TB endemic regions along with early anticipation of liver transplant is necessary, as in this case.

摘要

引言与重要性

布加综合征是一种因肝静脉流出道梗阻引起的罕见疾病。临床表现从无症状病例到需要进行肝移植的病例不等。该研究强调了诊断一例疑似腹部结核的布加综合征病例的重要性,因为抗结核药物本身可能会损害肝脏。

病例介绍

在此,我们报告一例18岁女性患者,表现为上腹部疼痛,伴有反复腹胀、黄疸和肝功能紊乱。此外,胸腔和腹腔积液中的腺苷脱氨酶水平升高,因此开始进行抗结核治疗,但由于她对这些药物出现不良反应而无法继续治疗。CT扫描后来显示出提示布加综合征的特征。最初,她接受了球囊血管成形术治疗,但病情最终恶化,需要进行肝移植。

临床讨论

布加综合征可能表现得较为隐匿,而且由于腹部结核非常不具有特异性,这两种情况可能非常容易混淆,尤其是在结核病流行地区。应进行详细的临床评估以及适当的检查和影像学检查以便早期识别,因为如果不及时治疗,这两种情况都与高发病率和死亡率相关。

结论

如本病例所示,在结核病流行地区,仔细调查并将布加综合征视为黄疸和肝功能紊乱伴腹水的重要病因,并尽早考虑肝移植是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803f/9577515/e63752f98c25/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803f/9577515/bd702a976253/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803f/9577515/e63752f98c25/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803f/9577515/bd702a976253/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803f/9577515/e63752f98c25/gr2.jpg

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本文引用的文献

1
Misdiagnosis of Budd Chiari syndrome, a case report from Afghanistan.布加综合征的误诊:来自阿富汗的一例病例报告
Ann Med Surg (Lond). 2022 Jan 1;73:103218. doi: 10.1016/j.amsu.2021.103218. eCollection 2022 Jan.
2
Mortality and health care burden of Budd Chiari syndrome in the United States: A nationwide analysis (1998-2017).美国布加综合征的死亡率和医疗负担:一项全国性分析(1998 - 2017年)
World J Hepatol. 2021 Jun 27;13(6):686-698. doi: 10.4254/wjh.v13.i6.686.
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Budd Chiari Syndrome and Intrahepatic Cholangiocarcinoma, An Unusual Combination: Case Report and Review of the Literature.
布加综合征与肝内胆管细胞癌的不常见组合:病例报告及文献复习。
Perm J. 2020 Nov;24:1-3. doi: 10.7812/TPP/19.204.
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The SCARE 2020 Guideline: Updating Consensus Surgical CAse REport (SCARE) Guidelines.SCARE 2020 指南:更新共识手术病例报告(SCARE)指南。
Int J Surg. 2020 Dec;84:226-230. doi: 10.1016/j.ijsu.2020.10.034. Epub 2020 Nov 9.
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Budd-Chiari syndrome as a complication of eosinophilic granulomatosis with polyangiitis in a young Chinese man: a case report.一名年轻中国男性中嗜酸性肉芽肿性多血管炎并发布加综合征:病例报告
J Int Med Res. 2020 Oct;48(10):300060520964352. doi: 10.1177/0300060520964352.
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Budd-Chiari syndrome: imaging review.布加综合征:影像学综述。
Br J Radiol. 2018 Dec;91(1092):20180441. doi: 10.1259/bjr.20180441. Epub 2018 Jul 24.
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Budd-Chiari syndrome and liver transplantation.布加综合征与肝移植
Intractable Rare Dis Res. 2015 Feb;4(1):24-32. doi: 10.5582/irdr.2014.01031.
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World J Gastroenterol. 2014 Oct 28;20(40):14831-40. doi: 10.3748/wjg.v20.i40.14831.
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Budd-Chiari syndrome management: Lights and shadows.布加综合征的治疗:光明与阴影
World J Hepatol. 2011 Oct 27;3(10):262-4. doi: 10.4254/wjh.v3.i10.262.
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Etiology, management, and outcome of the Budd-Chiari syndrome.布加综合征的病因、治疗及预后
Ann Intern Med. 2009 Aug 4;151(3):167-75. doi: 10.7326/0003-4819-151-3-200908040-00004.