Solitary lung myofibroma in an infant
Open Access
- 1 January 2021
- journal article
- research article
- Published by Elsevier in Journal of Pediatric Surgery Case Reports
- Vol. 64
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Mutations in PDGFRB Cause Autosomal-Dominant Infantile MyofibromatosisThe American Journal of Human Genetics, 2013
- Myofibroma—A Rare Entity with Unique Clinical PresentationJournal of Maxillofacial and Oral Surgery, 2011
- Infantile myofibromatosisPediatric Surgery International, 2007
- Solitary infantile gastrointestinal myofibroma: case reportJournal of Pediatric Surgery, 2005
- Infantile myofibromatosis: support for autosomal dominant inheritanceJournal of the American Academy of Dermatology, 2003
- Solitary intestinal fibromatosis: A rare cause of intestinal obstruction in neonate and infantJournal of Pediatric Surgery, 1991
- Myofibromatosis in AdultsAmerican Journal of Surgical Pathology, 1989
- Infantile myofibromatosis: The most common fibrous tumor of infancyJournal of Pediatric Surgery, 1988
- Fibromatosis and Fibrosarcoma of the Larynx and Pharynx in an InfantJAMA Otolaryngology–Head & Neck Surgery, 1985
- Congenital generalized fibromatosisPediatric Radiology, 1982