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 Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

643
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
643
Desmosomes01:05

Desmosomes

8.9K
The term desmosome derives from the Greek words "desmo" and "soma" meaning "adhesion bodies." This structure was first observed during the late 1800s and described as small, dense nodules in the epidermis. Desmosomes are button-like structures that help form an interlinked network of intermediate filaments across the cells. These junctions are  essential to hold cells together under mechanical stress and to maintain tissue integrity. Desmosomes are multi-protein...
8.9K

You might also read

Related Articles

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

Sort by
Same author

Gout, Hyperuricemia and Crystal-Associated Disease Network (G-CAN) consensus statement regarding labels and definitions for disease elements in calcium pyrophosphate crystal deposition (CPPD).

Annals of the rheumatic diseasesยท2026
Same author

Reliability of Radiographic Parameters in the Evaluation of Scapholunate Dissociation.

The Journal of hand surgeryยท2026
Same author

Nonvascularized Bone Grafting for Scaphoid Nonunion.

Journal of wrist surgeryยท2026
Same author

Do ChatGPT and Gemini's Recommendations Align With Established Guidelines for Hand and Upper Extremity Surgery?

Hand (New York, N.Y.)ยท2025
Same author

How I Do It: Three-Dimensional MR Neurography and Zero Echo Time MRI for Rendering of Peripheral Nerve and Bone.

Radiologyยท2025
Same author

Accuracy and Reliability of Video-Based Range-of-Motion Assessments in Postreconstruction Brachial Plexus Patients.

JB & JS open accessยท2025

Related Experiment Video

Updated: Mar 21, 2026

Human Dupuytren's Ex Vivo Culture for the Study of Myofibroblasts and Extracellular Matrix Interactions
08:59

Human Dupuytren's Ex Vivo Culture for the Study of Myofibroblasts and Extracellular Matrix Interactions

Published on: April 18, 2015

11.0K

Pachydermodactyly: A Case Report Including Histopathology.

Schneider K Rancy1, Richard D Granstein2, Manjula Bansal3

  • 1Division of Hand and Upper Extremity Surgery, Hospital for Special Surgery, New York, NY.

The Journal of Hand Surgery
|May 17, 2016
PubMed
Summary

Pachydermodactyly (PDD) is a rare fibromatosis causing painless swelling in fingers. This case highlights PDD mimicking inflammatory joint conditions, emphasizing the need for accurate diagnosis.

Keywords:
Pachydermodactylydigital fibromatosisproximal phalanxsoft tissue swelling

More Related Videos

A Protocol to Acquire the Degenerative Tenocyte from Humans
09:25

A Protocol to Acquire the Degenerative Tenocyte from Humans

Published on: June 9, 2018

7.7K

Related Experiment Videos

Last Updated: Mar 21, 2026

Human Dupuytren's Ex Vivo Culture for the Study of Myofibroblasts and Extracellular Matrix Interactions
08:59

Human Dupuytren's Ex Vivo Culture for the Study of Myofibroblasts and Extracellular Matrix Interactions

Published on: April 18, 2015

11.0K
A Protocol to Acquire the Degenerative Tenocyte from Humans
09:25

A Protocol to Acquire the Degenerative Tenocyte from Humans

Published on: June 9, 2018

7.7K

Area of Science:

  • Dermatology
  • Rheumatology
  • Pathology

Background:

  • Pachydermodactyly (PDD) is a rare digital fibromatosis.
  • It presents as painless soft tissue swelling, predominantly around the proximal interphalangeal joints.
  • PDD can involve the metacarpophalangeal joints, palm, and dorsum of the hand.

Observation:

  • PDD swelling near interphalangeal and metacarpophalangeal joints can be mistaken for juvenile inflammatory arthropathy.
  • PDD may coexist with inflammatory joint conditions.
  • This report details a case with bilateral proximal phalangeal involvement affecting multiple fingers.

Findings:

  • Clinical presentation of Pachydermodactyly.
  • Histopathologic findings in a PDD case.
  • Bilateral digital fibromatosis affecting index, middle, ring, and little fingers.

Implications:

  • Accurate differentiation of PDD from inflammatory arthropathies is crucial for appropriate patient management.
  • Understanding PDD's clinical and histopathologic features aids in diagnosis.
  • This case contributes to the literature on rare digital fibromatosis presentations.