Application of a pattern‐based approach to histological diagnosis in very early onset IBD (VEO‐IBD) in a multicentric cohort of children with emphasis on monogenic disease with IBD‐like morphology

Author:

Parente Paola1ORCID,Macciomei Maria C2,Buccoliero Anna M3,Santoro Luisa4,Cafferata Barbara5,Bifano Delfina6,Ferro Jacopo5,Vanoli Alessandro7ORCID,Fassan Matteo89,Angerilli Valentina8,Alaggio Rita10,Mastracci Luca1112,D'Armiento Maria13,Grillo Federica1112ORCID,Francalanci Paola10

Affiliation:

1. Pathology Unit Fondazione IRCCS Casa Sollievo della Sofferenza San Giovanni Rotondo Italy

2. Pathology Unit Azienda Ospedaliera San Camillo‐Forlanini Rome Italy

3. Pathology Unit Meyer Children's Hospital IRCCS Firenze Italy

4. Pathology Unit Azienda Ospedaliera Padova Padova Italy

5. Pathology Unit IRCCS Istituto Giannina Gaslini Genova Italy

6. Department of Pathology, ‘AORN Santobono Pausilipon’, Pediatric Hospital Naples Italy

7. Anatomic Pathology Unit, Department of Molecular Medicine University of Pavia, IRCCS San Matteo Hospital Pavia Italy

8. Department of Medicine (DIMED), Surgical Pathology Unit, Via Gabelli 61 University Hospital of Padua Padua Italy

9. Istituto Oncologico Veneto IOV‐IRCCS, Viale Gattamelata Padua Italy

10. Pathology Unit, Department of Laboratories IRCCS Bambino Gesù Children's Hospital Rome Italy

11. Pathology Unit IRCCS Ospedale Policlinico San Martino Genova Italy

12. Anatomic Pathology, Department of Surgical Sciences and Integrated Diagnostics (DISC) University of Genova Genoa Italy

13. Pathology Unit, Department of Public Health University of Naples Federico II Napoli Italy

Abstract

AimsVery early‐onset inflammatory bowel disease (VEO‐IBD) is a clinical umbrella term referring to IBD‐like symptoms arising in children before the age of 6 years, encompassing both ‘pure’ IBD, such as ulcerative colitis (UC) and Crohn's disease (CD) and monogenic diseases (MDs), the latter often involving genes associated with primary immunodeficiencies. Moreover, histological features in gastrointestinal (GI) biopsies in MD can also have IBD‐like morphology, making differential diagnosis difficult. Correct diagnosis is fundamental, as MDs show a more severe clinical course and their inadequate/untimely recognition leads to inappropriate therapy.Methods and resultsBiopsy samples from the lower and upper GI tract of 93 clinically diagnosed VEO‐IBD children were retrospectively selected in a multicentre cohort and histologically re‐evaluated by 10 pathologists blinded to clinical information. Each case was classified according to morphological patterns, including UC‐like; CD‐like; enterocolitis‐like; apoptotic; eosinophil‐rich; and IBD‐unclassified (IBD‐U). Nine (69%) MD children showed IBD‐like morphology; only the IBD‐U pattern correlated with MD diagnosis (P = 0.02) (available in 64 cases: 51 non‐MD, true early‐onset IBD/other; 13 MD cases). MD patients showed earlier GI symptom onset (18.7 versus 26.9 months) and were sent to endoscopy earlier (22 versus 37 months), these differences were statistically significant (P < 0.05). Upper GI histology was informative in 37 biopsies.ConclusionsThe diagnosis of the underlying cause of VEO‐IBD requires a multidisciplinary setting, and pathology, while being one of the fundamental puzzle pieces, is often difficult to interpret. A pattern‐based histological approach is therefore suggested, thus aiding the pathologist in VEO‐IBD reporting and multidisciplinary discussion.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

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