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Related Concept Videos

Pulmonary Hypertension: Classification and Pathogenesis01:30

Pulmonary Hypertension: Classification and Pathogenesis

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...
Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure01:16

Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure

Oxygen therapy has emerged as a significant tool in enhancing the quality of life for patients suffering from pulmonary arterial hypertension (PAH). While this therapy has principally been studied on patients with significant hypoxemia, this therapeutic approach helps prevent potential organ damage and can be administered in the comfort of one's home.
Oxygen therapy is vital in increasing and maintaining blood oxygen levels in PAH patients. As a result, it aids in reducing fatigue, improving...
Pneumothorax-II01:27

Pneumothorax-II

Pneumothorax is a medical condition defined by the buildup of air in the pleural space between the lungs and the chest wall. This accumulation of air can lead to partial or complete lung collapse, resulting in a range of clinical manifestations. Understanding the clinical presentation and effective management strategies is crucial for healthcare professionals in providing timely and appropriate care to individuals with pneumothorax.
Clinical Manifestations:
Pulmonary Embolism I: Introduction01:29

Pulmonary Embolism I: Introduction

Pulmonary embolism (PE) occurs when a thrombus, fat or air embolus, amniotic fluid, or tumor tissue blocks one or more pulmonary arteries. These blockages originate in the venous system or the right side of the heart.EtiologyPE primarily arises from deep vein thrombosis (DVT) and other hypercoagulable states, such as inherited thrombophilias. Additional etiological factors include venous stasis, commonly seen in obesity, and endothelial injury from surgery and trauma. Less common causes include...
Pulmonary Embolism II: Diagnostic Studies and Interprofessional Care01:29

Pulmonary Embolism II: Diagnostic Studies and Interprofessional Care

Diagnosing Pulmonary EmbolismDiagnosing pulmonary embolism (PE) involves clinical assessment and advanced imaging tests. The preferred diagnostic tool is the spiral (helical) CT scan or CT angiography (CTA), which uses intravenous contrast media to visualize the pulmonary vasculature and identify emboli.A ventilation-perfusion (V/Q) scan is an alternative for patients unable to receive contrast media. This scan includes both perfusion and ventilation scanning. Perfusion scanning involves...
Pulmonary Embolism I: Introduction01:19

Pulmonary Embolism I: Introduction

A blood clot, or thrombus, is a semi-solid mass composed of fibrin, platelets, and red blood cells. When it forms within a vessel, it can obstruct blood flow, known as thrombosis. If part of the clot detaches, it becomes an embolus that can travel and block distant vessels. When this occurs in the pulmonary arteries, it causes a condition known as pulmonary embolism (PE).Origin and ImpactMost often, the embolus originates from a thrombus in the deep veins of the lower limbs, a condition called...

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Related Experiment Video

Updated: Jul 9, 2026

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

Pulmonary hypertension after splenectomy?

M M Hoeper1, J Niedermeyer, F Hoffmeyer

  • 1Hannover Medical School, Germany.

Annals of Internal Medicine
|March 13, 1999
PubMed
Summary
This summary is machine-generated.

Patients who have undergone splenectomy (surgical removal of the spleen) may face a higher risk of developing pulmonary hypertension. This study found a significant association between asplenia and pulmonary hypertension.

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Last Updated: Jul 9, 2026

The Left Pneumonectomy Combined with Monocrotaline or Sugen as a Model of Pulmonary Hypertension in Rats
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Robot-Assisted Laparoscopic Splenectomy In Children: A Case Report with Literature Review

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Area of Science:

  • Pulmonary Medicine
  • Cardiology
  • Immunology

Background:

  • Asplenia, the absence of splenic function or the spleen, is increasingly recognized in patients with unexplained pulmonary hypertension.
  • Pulmonary hypertension (PH) is a serious condition characterized by high blood pressure in the lung arteries.

Purpose of the Study:

  • To investigate the clinical and histopathologic features of pulmonary hypertension in patients post-splenectomy.
  • To compare the prevalence of surgical asplenia in patients with idiopathic pulmonary hypertension versus other pulmonary diseases.

Main Methods:

  • A case series and case-control study design was employed.
  • Data were collected from 61 patients with pulmonary hypertension and 151 lung transplant recipients at a university hospital.
  • Histopathologic examination of lung specimens was performed.

Main Results:

  • The prevalence of asplenia was significantly higher in patients with pulmonary hypertension (11.5%) compared to controls (0%) (P < 0.001).
  • Histopathology revealed intimal fibrosis, plexiform lesions, and thrombotic lesions in the lungs of patients with postsplenectomy pulmonary hypertension.

Conclusions:

  • Splenectomy may represent a risk factor for the development of pulmonary hypertension.
  • Further research is warranted to elucidate the mechanisms linking asplenia and PH.