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

Glaucoma: Overview01:25

Glaucoma: Overview

Glaucoma is an eye condition characterized by increased intraocular pressure that damages the retina and optic nerve, leading to irreversible blindness if left untreated. The human eye has various components, including the cornea, iris, pupil, lens, and optic nerve. Aqueous humor is secreted by the epithelium of the ciliary body in the posterior chamber and flows through the trabecular meshwork and canal of Schlemm, maintaining normal intraocular pressure. The trabecular meshwork and the canal...

You might also read

Related Articles

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

Sort by
Same author

Cutaneous Melanoma in the Context of Aging.

Medicina (Kaunas, Lithuania)·2025
Same author

Understanding Merkel Cell Carcinoma: Pathogenic Signaling, Extracellular Matrix Dynamics, and Novel Treatment Approaches.

Cancers·2025
Same author

Author Correction: Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas.

Nature medicine·2025
Same author

AI-Based Analysis of Ziehl-Neelsen-Stained Sputum Smears for <i>Mycobacterium tuberculosis</i> as a Screening Method for Active Tuberculosis.

Life (Basel, Switzerland)·2024
Same author

Morphological and Immunohistochemical Aspects with Prognostic Implications and Therapeutic Targets of Primary Sinonasal Mucosal Melanoma: A Retrospective Study.

Cancers·2024
Same author

Clinical Tools for Optimizing Therapeutic Decision-Making in Prostate Cancer: A Five-Year Retrospective Analysis.

Life (Basel, Switzerland)·2024
Same journal

Letter to the Editor: Is Tissue Engineering a new histological paradigm?

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie·2026
Same journal

The connections between three Romanian centers of pathology outlined by Professor Augustin Mureşan (1908-1985).

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie·2026
Same journal

Primary NOS carcinoma arising in a lingual ectopic thyroid: diagnostic strategy and multidisciplinary management.

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie·2026
Same journal

Cauda equina cavernoma: case report and review of literature.

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie·2026
Same journal

Melanoma of unknown primary presenting as intestinal obstruction: a diagnostic challenge.

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie·2026
Same journal

Morphological properties of bone cement mixed with antibiotics.

Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie·2026
See all related articles

Related Experiment Video

Updated: May 15, 2026

A Patient-Derived Xenograft Model for Venous Malformation
06:51

A Patient-Derived Xenograft Model for Venous Malformation

Published on: June 15, 2020

Multiple disseminated glomuvenous malformations: do we know enough?

C Solovan1, Elena Chiticariu, Doina Beinsan

  • 1Department of Dermatology, Victor Babes University of Medicine and Pharmacy, Timisoara, Romania.

Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie
|January 11, 2013
PubMed
Summary
This summary is machine-generated.

Multiple glomuvenous malformations (GVMs), or glomangiomas, are rare vascular anomalies. This case highlights a familial GVM presentation in a young male, emphasizing its genetic basis and distinct histopathology.

More Related Videos

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model
05:12

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model

Published on: September 4, 2017

Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
14:58

Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations

Published on: October 20, 2017

Related Experiment Videos

Last Updated: May 15, 2026

A Patient-Derived Xenograft Model for Venous Malformation
06:51

A Patient-Derived Xenograft Model for Venous Malformation

Published on: June 15, 2020

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model
05:12

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model

Published on: September 4, 2017

Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
14:58

Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations

Published on: October 20, 2017

Area of Science:

  • Vascular Malformations
  • Dermatology
  • Genetics

Background:

  • Glomuvenous malformations (GVMs), also termed glomangiomas, are uncommon congenital vascular anomalies.
  • They exhibit a unique histology combining glomus cell proliferation and venous malformation characteristics.

Observation:

  • A 14-year-old male presented with multiple, disseminated dermal blue nodules.
  • A family history revealed similar asymptomatic lesions in his mother and maternal grandmother, suggesting autosomal dominant inheritance.

Findings:

  • Histopathological examination confirmed GVMs, characterized by cavernous vessels encircled by glomus cells.
  • Immunohistochemistry showed positivity for alpha smooth muscle actin, HHF35 (pan-actin), and h-caldesmon.

Implications:

  • This case underscores the genetic basis of GVMs, linked to mutations in the glomulin gene.
  • Understanding the clinical and histopathological features is crucial for diagnosing and managing this rare condition.