Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Infantile myofibromatosis.

M M Salamah1, S M Hammoudi, A R Sadi

  • 1Department of Pediatrics, Dhahran Health Center, Saudi Arabia.

Journal of Pediatric Surgery
|October 1, 1988
PubMed
Summary

Infantile myofibromatosis is a rare mesenchymal tumor affecting infants. This report details three pediatric cases and reviews existing literature on this condition.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Additive potential of ginger starch on antifungal potency of honey against Candida albicans.

Asian Pacific journal of tropical biomedicine·2013
Same author

Bilateral and synchronous cervical carcinoma in situ in a didelphic uterus.

International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics·1992
Same author

Acute splenic sequestration crises in Saudi children with sickle cell disease.

Annals of tropical paediatrics·1989
Same author

Lead poisoning: a report from Saudi Arabia.

American journal of diseases of children (1960)·1988
Same author

Idiopathic perforation of the biliary tract in infancy and childhood.

Journal of pediatric surgery·1988
Same author

Proptosis, skull infarction, and retro-orbital and epidural hematomas in a child with sickle cell disease.

Clinical pediatrics·1987

Area of Science:

  • Pediatric Oncology
  • Pediatric Pathology
  • Dermatology

Background:

  • Infantile myofibromatosis is a rare mesenchymal tumor.
  • It primarily affects infants and children.
  • This condition presents a diagnostic challenge due to its rarity.

Observation:

  • Three pediatric cases of infantile myofibromatosis were managed.
  • Clinical presentations varied among the affected children.
  • The cases highlight the diverse manifestations of the disorder.

Findings:

  • Infantile myofibromatosis can present as solitary or multiple lesions.
  • Histopathological examination is crucial for diagnosis.
  • Literature review indicates a spectrum of clinical behaviors.

Implications:

  • Early diagnosis and appropriate management are essential for affected infants.
  • Understanding the natural history aids in predicting outcomes.
  • Further research is needed to elucidate the pathogenesis and optimize treatment strategies.

Related Experiment Videos