Extra-appendiceal Mucinous Neoplasms: A Tumour with Clinicopathologic Similarities to Low- and High-Grade Appendiceal Counterpart.

colon extra-appendiceal mucinous neoplasms

Journal

Human pathology
ISSN: 1532-8392
Titre abrégé: Hum Pathol
Pays: United States
ID NLM: 9421547

Informations de publication

Date de publication:
25 Apr 2024
Historique:
received: 29 02 2024
revised: 15 04 2024
accepted: 18 04 2024
medline: 28 4 2024
pubmed: 28 4 2024
entrez: 27 4 2024
Statut: aheadofprint

Résumé

Appendiceal mucinous neoplasms feature neoplastic mucinous epithelium with pushing borders and densely fibrotic walls. We have identified five examples of analogous colorectal tumours. Slides, pathology reports, and clinical data were reviewed. Whole genome sequencing was performed in two cases. Three were women and the mean age was 70. Associated GI conditions included Crohn's disease [1], diverticulosis [2], and sarcoma of the terminal ileum [1]. Signs/symptoms included obstruction [2], nausea, vomiting, abdominal pain [1], and positive faecal immunohistochemical test [1]. Colonoscopic findings included narrowing [1], "fullness" [1], and caecal lesion concerning for GIST [1]. Tumours involved the rectosigmoid [2], sigmoid [1], transverse colon [1], and cecum [1] and ranged from 1.5 cm to 8.5 cm. All but one tumour arose in the setting of faecal stream abnormalities related to obstruction, diverticulosis, or bowel diversion. All cases showed columnar, variably mucinous epithelium associated with little-to-no lamina propria. All but one case showed fibrosis of the submucosa. Three cases had high-grade areas. Neoplastic glands and/or mucin dissected through the muscularis propria or subserosa in 3 examples. No extracolonic neoplastic cells/mucin, infiltrative invasion, or desmoplastic response were identified. Three patients with available follow-up [5.5 to 28 months] are alive. Whole genome sequencing identified pathogenic TP53 and ERBB2 variants, as well as ERBB2 copy number amplification in one high-grade example. Though these tumours share clinicopathologic characteristics with their appendiceal counterparts, our cohort is too small to draw solid conclusions. We propose the term "extra-appendiceal mucinous neoplasm [EAMN]" for these rare lesions.

Identifiants

pubmed: 38677555
pii: S0046-8177(24)00062-5
doi: 10.1016/j.humpath.2024.04.010
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have no conflicts of interest to report. There are no sources of support. Data are available upon request. This study has been approved by the JHH IRB.

Auteurs

Fengming Chen (F)

Department of Pathology, Duke University [work performed while at Johns Hopkins]. Electronic address: fengming.chen@duke.edu.

Samuel E Harvey (SE)

Department of Pathology, Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD, USA. Electronic address: sharve18@jhmi.edu.

Eric D Young (ED)

Department of Pathology, Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD, USA. Electronic address: eyoung50@jhmi.edu.

Tom Z Liang (TZ)

Department of Pathology, Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD, USA. Electronic address: tliang8@jh.edu.

Tatianna Larman (T)

Department of Pathology, Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD, USA. Electronic address: tlarman1@jhmi.edu.

Lysandra Voltaggio (L)

Department of Pathology, Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD, USA. Electronic address: lvoltag1@jhmi.edu.

Classifications MeSH