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An autopsy case of peliosis hepatis with X-linked myotubular myopathy.

Authors :
Funayama K
Shimizu H
Tanaka H
Kawachi I
Nishino I
Matsui K
Takahashi N
Koyama A
Katsuragi-Go R
Higuchi R
Aoyama T
Watanabe H
Kakita A
Takatsuka H
Source :
Legal medicine (Tokyo, Japan) [Leg Med (Tokyo)] 2019 May; Vol. 38, pp. 77-82. Date of Electronic Publication: 2019 Apr 18.
Publication Year :
2019

Abstract

This report describes the autopsy case of a 4-year-old boy who died from hepatic hemorrhage and rupture caused by peliosis hepatis with X-linked myotubular myopathy. Peliosis hepatis is characterized by multiple blood-filled cavities of various sizes in the liver, which occurs in chronic wasting disease or with the use of specific drugs. X-linked myotubular myopathy is one of the most serious types of congenital myopathies, in which an affected male infant typically presents with severe hypotonia and respiratory distress immediately after birth. Although each disorder is rare, 12 cases of pediatric peliosis hepatis associated with X-linked myotubular myopathy have been reported, including our case. Peliosis hepatis should be considered as a cause of hepatic hemorrhage despite its low incidence, and it requires adequate gross and histological investigation for correct diagnosis.<br /> (Copyright © 2019 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-4162
Volume :
38
Database :
MEDLINE
Journal :
Legal medicine (Tokyo, Japan)
Publication Type :
Academic Journal
Accession number :
31030121
Full Text :
https://doi.org/10.1016/j.legalmed.2019.04.005