BACKGROUND Congenital hallux varus(CHV)is a rare form of hallux varus deformity,characterized by medial deviation of the first toe at the metatarsophalangeal joint.It may be primary or secondary and presents clinicall...
BACKGROUND Immature ovarian teratoma is a rare and aggressive neoplasm that affects young women.This report is the first to describe the development of immature teratoma after ovarian cystectomy for mature teratoma of...
BACKGROUND Abernethy malformation,also known as congenital extrahepatic portosystemic shunt,is an uncommon malformation resulting from aberrant development of the portal venous system.Cystic fibrosis(CF)is an autosoma...
Supported by The Natural Science Foundation of Jilin Province,No.20200201475JC.
BACKGROUND Electromagnetic navigational bronchoscopy(ENB)is an emerging diagnostic tool that enables practitioners to biopsy peripheral lung tissues that were previously only accessible under computed tomography(CT)gu...
Supported by Science and Technology department of Sichuan Province,No.2020YFS0105;West China Second University Hospital of Sichuan University,No.KL036.
BACKGROUND Pulmonary lymphomatoid granulomatosis(PLG)is a lymphoproliferative disease associated with Epstein-Barr viral infection occurring mainly in adults and rarely in children.It is characterized by multiple pulm...
Supported by the Deanship of Scientific Research at Princess Nourah Bint Abdulrahman University Through the Fast-Track Research Funding Program.
BACKGROUND Hemangioma is a vascular benign tumour of endothelial origin.It appears commonly in the first decade of life with increases incidence in females.Hemangioma is not common to happen in the oral cavity and it ...
BACKGROUND There are multiple causes of sudden gastrointestinal bleeding in children.Reports of Dieulafoy lesions(DLs)in children are scarce.DLs can be fatal without appropriate treatment.CASE SUMMARY We present a ret...
BACKGROUND Tracheal tumors are relatively rare in adults and uncommon in children.Tracheal neurilemmoma is a rare condition in adults that usually affects middle-aged people,but it can also occur in children.Because t...
BACKGROUND Type A insulin resistance syndrome is a rare disorder caused by mutations in the gene encoding the insulin receptor.Its coexistence with ovarian serous papillary cystadenofibroma is even rarer.CASE SUMMARY ...
Supported by the National Natural Science Foundation of China,No.81573167;Science and Technology Project of Jiangsu,No.BE2017657
BACKGROUND Multisystemic smooth muscle dysfunction syndrome(MSMDS) is a rare genetic disease worldwide. The main mutation is the actin alpha 2(ACTA2) gene p.R179 H. In this paper, we report a Chinese MSMDS patient and...