Peritoneal or mesenteric tumours revealing histiocytosis

Bibliographic Details
Title: Peritoneal or mesenteric tumours revealing histiocytosis
Authors: Dominique Cazals-hatem, Fleur Cohen-Aubart, Julien Haroche, Abdellatif Tazi, Jean-François Emile, Andreas Seeber, Zofia Hélias-Rodzewicz, Jean Donadieu, Frédéric Charlotte, Janick Selves, Irena Ungureanu, Jerome Razanamahery, Peggy Dartigues, Manuela Delage-Corre, Patrick Tas, Sebastien Humbert, Alexandre Malakhia, Merja Kunnamo, Liana Veresezan, Chrystalla Prokopiou, Olivier Lucidarme
Source: BMJ Open Gastroenterology, Vol 8, Iss 1 (2021)
Publisher Information: BMJ Publishing Group, 2021.
Publication Year: 2021
Collection: LCC:Diseases of the digestive system. Gastroenterology
Subject Terms: Diseases of the digestive system. Gastroenterology, RC799-869
More Details: Objective Peritoneal or mesenteric tumours may correspond to several tumour types or tumour-like conditions, some of them being represented by histiocytosis. This rare condition often poses diagnostic difficulties that can lead to important time delay in targeted therapies. Our aim was to describe main features of histiocytoses with mesenteric localisation that can improve the diagnostic process.Design We performed a retrospective study on 22 patients, whose peritoneal/mesenteric biopsies were infiltrated by histiocytes.Results Abdominal pain was the revealing symptom in 10 cases, and 19 patients underwent surgical biopsies. The diagnosis of histiocytosis was proposed by initial pathologists in 41% of patients. The other initial diagnoses were inflammation (n=7), sclerosing mesenteritis (n=4) and liposarcoma (n=1). The CD163/CD68+CD1a- histiocytes infiltrated subserosa and/or deeper adipose tissues in 16 and 14 cases, respectively. A BRAFV600E mutation was detected within the biopsies in 11 cases, and two others were MAP2K1 mutated. The final diagnosis was histiocytosis in 18 patients, 15 of whom had Erdheim-Chester disease. The median diagnostic delay of histiocytosis was 9 months. Patients treated with BRAF or MEK inhibitors showed a partial response or a stable disease. One patient died soon after surgery, and five died by the progression of the disease.Conclusion Diagnosis of masses arising in the mesentery should be carefully explored as one of the possibilities in histiocytosis. This diagnosis is frequently missed on mesenteric biopsies. Molecular biology for detecting the mutations in BRAF or in genes of the MAP kinase pathway is a critical diagnostic tool.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2054-4774
Relation: https://bmjopengastro.bmj.com/content/8/1/e000622.full; https://doaj.org/toc/2054-4774
DOI: 10.1136/bmjgast-2021-000622
Access URL: https://doaj.org/article/e2005a2757d14fde9037e23c5e212d26
Accession Number: edsdoj.2005a2757d14fde9037e23c5e212d26
Database: Directory of Open Access Journals
More Details
ISSN:20544774
DOI:10.1136/bmjgast-2021-000622
Published in:BMJ Open Gastroenterology
Language:English