Adenomatoid tumours of the gastrointestinal tract - a case-series and review of the literature.

TitleAdenomatoid tumours of the gastrointestinal tract - a case-series and review of the literature.
Publication TypeJournal Article
Year of Publication2022
AuthorsHissong E, Graham RP, Wen KWah, Alpert L, Shi J, Lamps LW
JournalHistopathology
Volume80
Issue2
Pagination348-359
Date Published2022 Jan
ISSN1365-2559
KeywordsAdenomatoid Tumor, Adult, Aged, Biomarkers, Tumor, Female, Gastrointestinal Neoplasms, Humans, Immunohistochemistry, Male, Middle Aged
Abstract

AIMS: Adenomatoid tumours are mesothelial-derived benign neoplasms with a predilection for the genital tract. Extragenital sites are rare and can cause significant diagnostic challenges. Herein, we describe the clinicopathological features of a cohort of adenomatoid tumours involving the gastrointestinal tract and liver in order to more clearly characterise their histological findings and aid in diagnosis.

METHODS AND RESULTS: The pathology databases at four institutions were searched for adenomatoid tumours involving the gastrointestinal tract or liver, yielding eight cases. Available clinicoradiological and follow-up data were collected from the medical records. Six tumours were incidentally discovered during imaging studies or at the time of surgical exploration for unrelated conditions; presenting symptoms were unknown in two patients. Histologically, the tumours were well-circumscribed, although focal ill-defined borders were present in four cases. No infiltration of adjacent structures was identified. Architectural heterogeneity was noted in five (63%) tumours; an adenoid pattern often predominated. The neoplastic cells were flattened to cuboidal with eosinophilic cytoplasm. Cytoplasmic vacuoles mimicking signet ring-like cells were present in five (63%) cases. Three (38%) cases showed involvement of the mesothelium with reactive mesothelial hyperplasia. Cytological atypia or increased mitotic activity was not identified. The surrounding stroma ranged from oedematous/myxoid to densely hyalinised. Immunohistochemistry confirmed mesothelial origin in all cases evaluated. No patients developed recurrence of disease.

CONCLUSIONS: The current study evaluates the clinicopathological findings in a collective series of gastrointestinal and hepatic adenomatoid tumours, correlating with those described in individually reported cases. We highlight common histological features and emphasise variable findings that could mimic a malignant neoplasm.

DOI10.1111/his.14553
Alternate JournalHistopathology
PubMed ID34480486
PubMed Central IDPMC8712375
Grant ListK08 CA234222 / CA / NCI NIH HHS / United States
K08CA234222 / NH / NIH HHS / United States
Related Faculty: 
Erika Hissong, M.D.

Pathology & Laboratory Medicine 1300 York Avenue New York, NY 10065 Phone: (212) 746-6464
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