| Literature DB >> 32372511 |
Seiichi Shimizu1, Seisuke Sakamoto1, Akinari Fukuda1, Yusuke Yanagi1, Hajime Uchida1, Masahiro Takeda1, Yohei Yamada2, Noriyuki Nakano3, Takako Yoshioka3, Mureo Kasahara1.
Abstract
X-linked myotubular myopathy (MTM) (OMIM 310400) is a severe neuromuscular disorder caused by mutations in the myotubularin (MTM1) gene. Liver hemorrhaging due to peliosis hepatis (PH) is a fatal complication. We herein report 2 successful cases of living-donor liver transplantation (LDLT) for MTM patients due to liver hemorrhaging caused by PH and review previous reports. A boy who was 9 years and 4 months old initially underwent left lateral segmentectomy due to massive hepatic and intraperitoneal hemorrhaging. As bleeding from the remnant liver continued after hepatectomy, this patient emergently underwent LDLT using a left lateral segment graft from his father. Another boy who was 1 year and 7 months old underwent transcatheter arterial embolization due to hepatic hemorrhaging and was referred to our hospital for LDLT using a left lateral segment graft from his father. The pathological findings in both cases showed sinusoidal dilatation with degenerative changes in reticular fiber and hematoma in the explanted liver, which were consistent with PH associated with MTM. LT should be considered as a treatment option for patients with episodes of hepatic hemorrhaging due to MTM in order to protect against fatal bleeding.Entities:
Keywords: clinical research/practice; critical care/intensive care management; liver disease: congenital; liver transplantation/hepatology; liver transplantation: living donor
Mesh:
Year: 2020 PMID: 32372511 DOI: 10.1111/ajt.15978
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086