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Review
. 2019 Feb;39(1):36-39.
doi: 10.1016/j.annpat.2018.08.007. Epub 2018 Oct 12.

[Diffuse esophageal leiomyomatosis and Alport's syndrome: A case report and review of the literature]

[Article in French]
Affiliations
Review

[Diffuse esophageal leiomyomatosis and Alport's syndrome: A case report and review of the literature]

[Article in French]
Clemence Delteil et al. Ann Pathol. 2019 Feb.

Abstract

Diffuse esophageal leiomyomatosis is a rare esophageal tumor characterized by circumferential thickening of smooth muscle layers. Diffuse esophageal leiomyomatosis can be associated with Alport's syndrome and therefore diagnosed by skin biopsy. Alport syndrome is a hereditary disease usually defined by the association of glomerular nephropathy and perceptual deafness. Here we describe the management of a young women with a diffuse esophageal leiomyomatosis and a past history of uterine leiomyoma. The surgical treatment depends on the esophageal extent of the disease. Association between diffuse esophageal leiomyomatosis and early uterine leiomyomas could be also observed and leading to Alport's syndrome diagnosis despite the absence of renal abnormalities.

Keywords: Alport's syndrome; Chirurgie œsophagienne; Diffuse esophageal leiomyomatosis; Dysphagia; Dysphagie; Esophageal surgery; Immunochemistry; Immunochimie; Léiomyomatose œsophagienne diffuse; Syndrome d’Alport.

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