Ultraschall Med 2011; 32(3): 311-312
DOI: 10.1055/s-0029-1245532
Kasuistik/Case Report

© Georg Thieme Verlag KG Stuttgart · New York

Ultrasound: A Helpful Diagnostic Tool in Esophageal Leiomyomatosis with Alport Syndrome

Ultraschalldiagnostik bei ösophagealer Leiomyomatose und Alport-SyndromC. Denne, H. Hahn, M. Steinborn, S. Hosie, J.-C. Lenz, F. Höpner, S. Burdach
Weitere Informationen

Publikationsverlauf

received: 5.1.2010

accepted: 20.5.2010

Publikationsdatum:
07. Juli 2010 (online)

Introduction

Esophageal leiomyomatosis is a rare condition causing leiomyomatous thickening of all or part of the esophagus. It occurs predominantly in children and younger adults (Lonsdale RN et al. Familial oesophageal leiomyomatosis and nephropathy. Histopathology 1992; 20: 127 – 133). Patients usually present with progressive dysphagia and other gastrointestinal complaints such as acid reflux (Fernandes JP et al. Diffuse leiomyomatosis of the esophagus. Digest Dis 1975; 20: 684 – 690). Alport’s syndrome is a genetic disorder that is mainly inherited as a dominant X-linked trait and is caused by mutations in the collagen type 4 biosynthesis genes (Antignac C et al. Alport syndrome and diffuse leiomyomatosis: Deletions in the 5’ end of the COL4A5 collagen gene. Kidney Int 1992; 42: 1178 – 1183). It is characterized by glomerulonephritis progressing to endstage kidney disease and hearing loss and can also affect the eyes. The prevalence of Alport’s syndrome is estimated to be about 1 in 7500. 80 % are males. The conincidence with diffuse leiomyomatosis has been reported in about 5 % of all Alport patients.

Dr. Christian Denne

Pediatrics, Technische Universität München

Kölner Platz 1

80804 München

Germany

Telefon: ++ 49/17 09 58 34 21

Fax: ++ 49/89/30 00 10 30

eMail: denne.christian@gmx.net