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疑似患有先天性巨结肠症儿童的全层直肠活检:不确定的活检结果

Full-Thickness Rectal Biopsy in Children Suspected of Having Hirschsprung's Disease: The Inconclusive Biopsy.

作者信息

Korsager Leise Elisabeth Hviid, Bjørn Niels, Ellebæk Mark Bremholm, Christensen Lene Gaardsmand, Qvist Niels

机构信息

Research Unit for Surgery, Odense University Hospital, University of Southern Denmark, 5230 Odense, Denmark.

Centre of Excellence in Gastrointestinal Diseases and Malformations in Infancy and Childhood (GAIN), Odense University Hospital, 5000 Odense, Denmark.

出版信息

Children (Basel). 2023 Sep 28;10(10):1619. doi: 10.3390/children10101619.

Abstract

The diagnosis of Hirschsprung's disease relies on histologically proven aganglionosis and nerve trunk hypertrophy in rectal biopsies. Although the frequency of inconclusive biopsies is relatively low, it is a relevant clinical problem. The aim of the present study was to investigate whether a re-evaluation of archived full-thickness biopsies (FTBs) stained with hematoxylin and eosin (HE), together with immune histochemical (IHC) staining, would be diagnostic in biopsies otherwise deemed inconclusive at initial examination with HE only. A total of 34 inconclusive biopsies in 31 patients were identified. From each tissue block, three slices were cut and stained with HE, S100 and calretinin. A blinded pathologist examined the tissue samples. At re-evaluation, one patient was found positive for HD and 11 negative for HD with both HE and IHC staining, respectively. In all 12 cases, the result was confirmed by the final diagnosis at a 5-year follow-up. The rest of the cases were deemed inconclusive. A re-evaluation of the remaining tissue from the biobank might have saved one third of the children from a re-biopsy. The value of adding IHC to conventional HE staining is dubious.

摘要

先天性巨结肠症的诊断依赖于直肠活检组织学证实的无神经节细胞症和神经干肥大。尽管活检结果不确定的频率相对较低,但这仍是一个相关的临床问题。本研究的目的是调查对存档的苏木精和伊红(HE)染色的全层活检(FTB)进行重新评估,并结合免疫组织化学(IHC)染色,是否能对仅用HE进行初次检查时被认为不确定的活检做出诊断。共确定了31例患者的34份不确定活检样本。从每个组织块中切取三片,分别用HE、S100和钙结合蛋白进行染色。一位不知情的病理学家对组织样本进行检查。重新评估时,分别有1例患者经HE和IHC染色诊断为先天性巨结肠症阳性,11例为阴性。在所有这12例病例中,5年随访的最终诊断证实了结果。其余病例被认为结果不确定。对生物样本库中剩余组织进行重新评估可能会使三分之一的儿童免于再次活检。在传统HE染色中加入IHC的价值值得怀疑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2a7/10605644/75cc26c60ef1/children-10-01619-g001.jpg

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