| Literature DB >> 31030121 |
Kazuhisa Funayama1, Hiroshi Shimizu2, Hidetomo Tanaka2, Izumi Kawachi3, Ichizo Nishino4, Kou Matsui5, Naoya Takahashi6, Akihide Koyama1, Rieka Katsuragi-Go7, Ryoko Higuchi8, Takashi Aoyama8, Hiraku Watanabe8, Akiyoshi Kakita2, Hisakazu Takatsuka9.
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.Entities:
Keywords: Autopsy; Hepatic hemorrhage; Intraperitoneal hemorrhage; Peliosis hepatis; X-linked myotubular myopathy
Mesh:
Year: 2019 PMID: 31030121 DOI: 10.1016/j.legalmed.2019.04.005
Source DB: PubMed Journal: Leg Med (Tokyo) ISSN: 1344-6223 Impact factor: 1.376