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

Generalized atrophic dells in a newborn.

Robert L Buka1, Brandie J Roberts, Brooke Resh

  • 1Division of Pediatric Dermatology, Children's Hospital, San Diego, California, USA. rbuka@md.northwestern.edu

Cutis
|August 15, 2006
PubMed
Summary
This summary is machine-generated.

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

Intracranial mesenchymal tumor, FET::CREB fusion-positive: An integrative analysis of 81 cases.

Neuro-oncology·2026
Same author

Rare presentation of juvenile xanthogranuloma in the posterior fossa of a toddler.

BMJ case reports·2021
Same author

Congenital cutaneous non-neural granular cell tumor mimicking herpetic infection: Case report and review of the literature.

Pediatric dermatology·2021
Same author

Non-invasive intradermal imaging of cystine crystals in cystinosis.

PloS one·2021
Same author

Rare case of extranodal Rosai-Dorfman disease presenting as a middle cranial fossa tumour.

BMJ case reports·2021
Same author

Plasminogen Activator Inhibitor-1 as a Marker of Esophageal Functional Changes in Pediatric Eosinophilic Esophagitis.

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association·2020
Same journal

Black Dots on the Scalp of a Child.

Cutis·2026
Same journal

Psoriasis and Obesity: A Clinical Review of the Bidirectional Link and Management Implications.

Cutis·2026
Same journal

Adalimumab in Lichen Planus: A Narrative Review of Treatment and Paradoxical Reactions.

Cutis·2026
Same journal

The Future of Psoriasis Care.

Cutis·2026
Same journal

Evaluating GPT-4o for Automated Classification of Skin Lesions Using the HAM10000 Dataset.

Cutis·2026
Same journal

Metastatic Primary Extramammary Paget Disease: A Case Series.

Cutis·2026
See all related articles

Infantile myofibromatosis (IM) is a rare, locally invasive tumor. This report details an unusual case of the atrophic variant of infantile myofibromatosis.

Area of Science:

  • Pediatric Oncology
  • Dermatopathology
  • Soft Tissue Tumors

Background:

  • Infantile myofibromatosis (IM) is a benign, locally invasive neoplasm presenting in infancy.
  • Its behavior is often hamartomatous, with uncertain cellular origin (fibroblast vs. smooth muscle myocyte).
  • Lesions vary in size and typically do not metastasize.

Purpose of the Study:

  • To report an unusual case of infantile myofibromatosis.
  • To highlight the atrophic variant of this rare condition.

Main Methods:

  • Case presentation of a patient with infantile myofibromatosis.
  • Clinical and pathological review of the atrophic variant.

Main Results:

  • The patient presented with an unusual manifestation of infantile myofibromatosis.

Related Experiment Videos

  • The atrophic variant represents a distinct clinical presentation of IM.
  • Conclusions:

    • Infantile myofibromatosis can present with diverse morphologies, including an atrophic variant.
    • Further research may clarify the specific cell of origin and behavior of different IM variants.