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先天性巨结肠症的早期检测与干预:成功治疗的关键

Early Detection and Intervention for Hirschsprung's Disease: A Key to Successful Outcomes.

作者信息

Rathi Karishma, Verma Aanya, Pingat Priyanka

机构信息

Assistant Professor of the Department of Pharmacy Practice at Dr. D.Y. Patil Institute of Pharmaceutical Sciences and Research Pimpri, Pune.

Pharm D Intern, Department of Pharmacy Practice at Dr. D.Y. Patil Institute of Pharmaceutical Sciences and Research Pimpri, Pune.

出版信息

Clin Med Insights Case Rep. 2024 Jan 23;17:11795476241226577. doi: 10.1177/11795476241226577. eCollection 2024.

DOI:10.1177/11795476241226577
PMID:38269147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10807328/
Abstract

Hirschsprung's disease is a congenital disorder characterized by the absence of nerve cells in the colon muscles, leading to difficulties in evacuating stool. This case report describes a newborn patient presenting with typical symptoms of the disease, including abdominal distension, constipation, diarrhea, and fever. The patient's initial laboratory investigations revealed anemia (Hb: 9.80 g/dL), low RBC count (3.50 million/cu mm), elevated RDW (16.70%), increased WBC count (11 000/cu mm), and raised platelet levels (891 000/µL) along with an elevated CRP (3.22). The baby received a comprehensive treatment regimen, including blood transfusion, Syp. MVBC, Enterogermina, Inj. Pan, Inj. Metro, Inj. Piptaz, Inj. Vancomycin, Calcium gluconate, and Inj. Aminoven. Following this treatment and necessary surgical intervention, the patient demonstrated significant improvement in frequent bowel movements and alleviation of other symptoms. This case highlights the importance of prompt diagnosis and multidisciplinary management for favorable outcomes in infants with Hirschsprung's disease.

摘要

先天性巨结肠是一种先天性疾病,其特征是结肠肌肉中缺乏神经细胞,导致排便困难。本病例报告描述了一名出现该疾病典型症状的新生儿患者,这些症状包括腹胀、便秘、腹泻和发热。患者最初的实验室检查结果显示贫血(血红蛋白:9.80 g/dL)、红细胞计数低(350万/立方毫米)、红细胞分布宽度升高(16.70%)、白细胞计数增加(11000/立方毫米)、血小板水平升高(891000/微升)以及C反应蛋白升高(3.22)。该婴儿接受了综合治疗方案,包括输血、复方胃蛋白酶合剂、亿活、泮托拉唑注射液、甲硝唑注射液、哌拉西林他唑巴坦注射液、万古霉素注射液、葡萄糖酸钙和复方氨基酸注射液。经过这种治疗和必要的手术干预后,患者在频繁排便方面有了显著改善,其他症状也有所缓解。本病例强调了对先天性巨结肠婴儿进行及时诊断和多学科管理以取得良好预后的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4997/10807328/26558b793b1e/10.1177_11795476241226577-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4997/10807328/e7e3c5a118ea/10.1177_11795476241226577-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4997/10807328/c3db7bd2f3c3/10.1177_11795476241226577-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4997/10807328/26558b793b1e/10.1177_11795476241226577-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4997/10807328/e7e3c5a118ea/10.1177_11795476241226577-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4997/10807328/c3db7bd2f3c3/10.1177_11795476241226577-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4997/10807328/26558b793b1e/10.1177_11795476241226577-fig3.jpg

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Orphanet J Rare Dis. 2020 Jun 25;15(1):164. doi: 10.1186/s13023-020-01362-3.
2
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Pediatr Dev Pathol. 2020 Jan-Feb;23(1):8-22. doi: 10.1177/1093526619892351. Epub 2019 Dec 2.
3
Hirschsprung's disease: the importance of early diagnosis.先天性巨结肠:早期诊断的重要性。
Autops Case Rep. 2013 Sep 30;3(3):59-66. doi: 10.4322/acr.2013.030. eCollection 2013 Jul-Sep.
4
Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes.先天性巨结肠症——整合基础科学和临床医学以改善治疗效果。
Nat Rev Gastroenterol Hepatol. 2018 Mar;15(3):152-167. doi: 10.1038/nrgastro.2017.149. Epub 2018 Jan 4.
5
Hirschsprung's disease in the UK and Ireland: incidence and anomalies.英国和爱尔兰的先天性巨结肠症:发病率与异常情况
Arch Dis Child. 2017 Aug;102(8):722-727. doi: 10.1136/archdischild-2016-311872. Epub 2017 Mar 9.
6
DIAGNOSTIC ACCURACY OF BARIUM ENEMA FINDINGS IN HIRSCHSPRUNG'S DISEASE.钡剂灌肠检查结果在先天性巨结肠症中的诊断准确性
Arq Bras Cir Dig. 2016 Jul-Sep;29(3):155-158. doi: 10.1590/0102-6720201600030007.
7
How to manage a late diagnosed Hirschsprung's disease.如何处理迟发性诊断的先天性巨结肠症。
Afr J Paediatr Surg. 2016 Apr-Jun;13(2):82-7. doi: 10.4103/0189-6725.182562.
8
The value of the 24-h delayed abdominal radiograph of barium enema in the diagnosis of Hirschsprung's disease.钡剂灌肠24小时延迟腹部X线片在先天性巨结肠症诊断中的价值。
Pediatr Surg Int. 2015 Jan;31(1):11-5. doi: 10.1007/s00383-014-3632-5. Epub 2014 Oct 28.
9
Prevention and control system of hypokalemia in fast recovery after abdominal surgery.腹部手术后快速康复中低钾血症的防治体系
Curr Ther Res Clin Exp. 2013 Jun;74:68-73. doi: 10.1016/j.curtheres.2013.02.004.
10
Advances in Hirschsprung disease genetics and treatment strategies: an update for the primary care pediatrician.先天性巨结肠症遗传学与治疗策略的进展:给基层儿科医生的最新资讯
Clin Pediatr (Phila). 2014 Jan;53(1):71-81. doi: 10.1177/0009922813500846. Epub 2013 Sep 3.