Literature DB >> 9391196

The significance of biliary sludge in children with sickle cell disease.

A H Al-Salem1, S Qaisruddin.   

Abstract

The prevalence of cholelithiasis was studied prospectively by abdominal ultrasound (US) examination in 305 children with sickle cell disease aged 1-18 years (mean 10.45). Gallstones were present in 60 children (19.7%); an additional 50 had biliary sludge only (16.4%). On follow-up of 35 of the 50 children with sludge, 23 (65.7%) had developed gallstones and 5 had already had a cholecystectomy. Five continued to have sludge on follow-up while 7 were reported to have no sludge. Children with US evidence of sludge should be followed up regularly by US, and those who develop gallstones should undergo elective cholecystectomy. For those with biliary sludge only, we recommend elective cholecystectomy if there are hepatobiliary symptoms.

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Year:  1998        PMID: 9391196     DOI: 10.1007/s003830050233

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  9 in total

1.  Hepatobiliary Complications of Sickle Cell Disease among Children Admitted to Al Wahda Teaching Hospital, Aden, Yemen.

Authors:  Hana A Qhalib; Gamal H Zain
Journal:  Sultan Qaboos Univ Med J       Date:  2014-10-14

2.  Outcome of cholelithiasis in Sudanese children with Sickle Cell Anaemia (SCA) after 13 years follow-up.

Authors:  B A I Attalla; Z A Karrar; G Ibnouf; A O Mohamed; O Abdelwahab; E M Nasir; M A El Seed
Journal:  Afr Health Sci       Date:  2013-03       Impact factor: 0.927

3.  Diagnostic and therapeutic ERCP in the pediatric age group.

Authors:  Hussain Issa; Ali Al-Haddad; Ahmed H Al-Salem
Journal:  Pediatr Surg Int       Date:  2006-12-06       Impact factor: 1.827

4.  Abdominal ultrasound with scintigraphic and clinical correlates in infants with sickle cell anemia: baseline data from the BABY HUG trial.

Authors:  M Beth McCarville; Zhaoyu Luo; Xiangke Huang; Renee C Rees; Zora R Rogers; Scott T Miller; Bruce Thompson; Ram Kalpatthi; Winfred C Wang
Journal:  AJR Am J Roentgenol       Date:  2011-06       Impact factor: 3.959

Review 5.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

6.  Pediatric Cholecystectomy: Clinical Significance of Cases Unrelated to Hematologic Disorders.

Authors:  Hae-Young Kim; Soo-Hong Kim; Yong-Hoon Cho
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2015-06-29

7.  A case of incidental infantile gallbladder adenomyomatosis: an unusual US finding of uncertain clinical significance.

Authors:  Elena Drakonaki; Stamatios Kokkinakis; Ioannis Karageorgiou; Neofytos Maliotis; Anna Ioannidoy; Emmanouil K Symvoulakis
Journal:  J Ultrason       Date:  2020-12-18

Review 8.  Hepatobiliary Manifestations of Sickle Cell Anemia.

Authors:  Hussain Issa; Ahmed H Al-Salem
Journal:  Gastroenterology Res       Date:  2010-01-20

9.  Common hepatic duct perforation in a sickle cell disease child.

Authors:  Talal A Al-Malki; Ashraf H M Ibrahim
Journal:  Ann Saudi Med       Date:  2004 Jan-Feb       Impact factor: 1.526

  9 in total

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