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

Pulmonary Hypertension: Classification and Pathogenesis01:30

Pulmonary Hypertension: Classification and Pathogenesis

149
Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
There are various classifications for PH, each relating to different underlying causes and also...
149

You might also read

Related Articles

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

Sort by
Same author

Alteration in cerebral cortex thickness and structural covariance networks in patients with chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS).

Frontiers in neurology·2026
Same author

Well-differentiated HPV-independent gastric-type adenocarcinoma of the cervix: a case report and literature review.

Frontiers in oncology·2025
Same author

SHP1 overexpression ameliorates renal fibrosis via inhibition of STAT3 signaling and glycolysis reprogramming.

Scientific reports·2025
Same author

Propionic acid mediates the renoprotective effects of fecal microbiota transplantation against ischemia-reperfusion injury via upregulating GPR43.

Frontiers in cellular and infection microbiology·2025
Same author

Correction to: Association of T1-weighted hyperintensity with timing of peak bilirubin levels in neonates with hyperbilirubinemia.

Neuroradiology·2025
Same author

Association of T1-weighted hyperintensity with timing of peak bilirubin levels in neonates with hyperbilirubinemia.

Neuroradiology·2025

Related Experiment Video

Updated: Jun 2, 2025

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

A Patient-Derived Xenograft Model for Venous Malformation

Published on: June 15, 2020

5.3K

Pulmonary cavernous hemangioma: a case report.

Wei Li1, Xingxing Zheng1, Hongzhe Tian1

  • 1Department of Medical Imaging, Baoji Central Hospital, Baoji, China.

BMC Pulmonary Medicine
|January 17, 2025
PubMed
Summary
This summary is machine-generated.

Pulmonary cavernous hemangiomas (PCH) are rare lung tumors. This case report details a surgically resected PCH in a young patient, highlighting its diagnostic challenges and successful treatment.

Keywords:
Case reportChest computed tomography (CT)Pulmonary cavernous hemangioma (PCH)Solitary nodules in the lungVideo-assisted thoracoscopic surgery (VATS)

More Related Videos

Left Atrial Stenosis Induced Pulmonary Venous Arterialization and Group 2 Pulmonary Hypertension in Rat
08:34

Left Atrial Stenosis Induced Pulmonary Venous Arterialization and Group 2 Pulmonary Hypertension in Rat

Published on: November 18, 2018

7.1K
The Left Pneumonectomy Combined with Monocrotaline or Sugen as a Model of Pulmonary Hypertension in Rats
07:29

The Left Pneumonectomy Combined with Monocrotaline or Sugen as a Model of Pulmonary Hypertension in Rats

Published on: March 8, 2019

10.7K

Related Experiment Videos

Last Updated: Jun 2, 2025

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

A Patient-Derived Xenograft Model for Venous Malformation

Published on: June 15, 2020

5.3K
Left Atrial Stenosis Induced Pulmonary Venous Arterialization and Group 2 Pulmonary Hypertension in Rat
08:34

Left Atrial Stenosis Induced Pulmonary Venous Arterialization and Group 2 Pulmonary Hypertension in Rat

Published on: November 18, 2018

7.1K
The Left Pneumonectomy Combined with Monocrotaline or Sugen as a Model of Pulmonary Hypertension in Rats
07:29

The Left Pneumonectomy Combined with Monocrotaline or Sugen as a Model of Pulmonary Hypertension in Rats

Published on: March 8, 2019

10.7K

Area of Science:

  • Cardiovascular Medicine
  • Pulmonary Medicine
  • Oncology

Background:

  • Pulmonary cavernous hemangiomas (PCH) are rare vascular malformations.
  • They can mimic malignant lung tumors, posing diagnostic challenges.
  • Surgical resection is often curative for symptomatic or suspicious PCH.

Purpose of the Study:

  • To report a rare case of a surgically resected pulmonary cavernous hemangioma.
  • To review the clinical, imaging, and histopathological features of PCH.
  • To enhance understanding of PCH diagnosis and management.

Main Methods:

  • A case of a 16-year-old patient with a suspected lung tumor was presented.
  • Diagnostic workup included chest X-ray, CT scan, and tumor markers.
  • Surgical excision was performed for definitive diagnosis and treatment.
  • Post-operative histological examination confirmed pulmonary cavernous hemangioma.

Main Results:

  • Imaging revealed irregular soft tissue lesions with enhancement and spicules in the right upper lung lobe.
  • Mediastinal lymphadenopathy was noted, raising suspicion for malignancy.
  • Histopathology confirmed the lesion as a pulmonary cavernous hemangioma.
  • The patient experienced no recurrence post-surgery.

Conclusions:

  • Pulmonary cavernous hemangiomas can present as suspicious lung lesions requiring surgical intervention.
  • Multimodality imaging and histopathology are crucial for accurate PCH diagnosis.
  • Surgical resection offers a definitive treatment for pulmonary cavernous hemangiomas.