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Esophageal Melanocytosis: report of two cases and review of a rare and misunderstood entity.

Authors :
UCL - (SLuc) Service d'anatomie pathologique
Dubail, A
Dano, H
de Suray, N
Hassaini, H
Jouret-Mourin, A
UCL - (SLuc) Service d'anatomie pathologique
Dubail, A
Dano, H
de Suray, N
Hassaini, H
Jouret-Mourin, A
Source :
Acta gastro-enterologica Belgica, Vol. 85, no.2, p. 390-392 (2022)
Publication Year :
2022

Abstract

Esophageal melanocytosis (EM) is a rare entity, which is characterized by a non-atypical melanocytic proliferation and melanin deposits in the esophageal mucosa. The confusion between the terms of melanosis and melanocytosis in the literature, the rarity of this lesion (less than 50 cases reported in the literature), its uncertain pathobiological course and the lack of experience of pathologists and gastroenterologists prompt us to draw the attention to this particular entity by reporting two cases and reviewing the literature. Magnifying endoscopy to observe intensive melanin accumulation followed by a biopsy are key for the diagnosis.

Details

Database :
OAIster
Journal :
Acta gastro-enterologica Belgica, Vol. 85, no.2, p. 390-392 (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372955943
Document Type :
Electronic Resource