Lymphedema praecox: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
CSV import
 
Line 20: Line 20:
}}
}}
{{Short description|A genetic condition causing lymphedema in young individuals}}
{{Short description|A genetic condition causing lymphedema in young individuals}}
== Lymphedema praecox ==
'''Lymphedema praecox''' is a form of primary [[lymphedema]] that typically presents during adolescence or early adulthood. It is characterized by the abnormal accumulation of lymphatic fluid, leading to swelling, most commonly in the lower extremities. This condition is often hereditary and can significantly impact the quality of life of affected individuals.
'''Lymphedema praecox''' is a form of primary [[lymphedema]] that typically presents during adolescence or early adulthood. It is characterized by the abnormal accumulation of lymphatic fluid, leading to swelling, most commonly in the lower extremities. This condition is often hereditary and can significantly impact the quality of life of affected individuals.
=== Pathophysiology ===
=== Pathophysiology ===

Latest revision as of 22:08, 8 April 2025

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Lymphedema praecox
Synonyms Meige disease
Pronounce N/A
Specialty N/A
Symptoms Swelling of the lower limbs, heaviness, restricted range of motion
Complications Infection, skin changes, psychosocial issues
Onset Typically between ages 1 and 35
Duration Long-term
Types N/A
Causes Genetic mutation
Risks Family history, female gender
Diagnosis Physical examination, imaging studies
Differential diagnosis Lipedema, chronic venous insufficiency
Prevention None
Treatment Compression therapy, manual lymphatic drainage, exercise
Medication N/A
Prognosis Variable, often manageable with treatment
Frequency Rare
Deaths N/A


A genetic condition causing lymphedema in young individuals


Lymphedema praecox is a form of primary lymphedema that typically presents during adolescence or early adulthood. It is characterized by the abnormal accumulation of lymphatic fluid, leading to swelling, most commonly in the lower extremities. This condition is often hereditary and can significantly impact the quality of life of affected individuals.

Pathophysiology[edit]

Lymphedema praecox is primarily caused by developmental abnormalities in the lymphatic system. These abnormalities can include hypoplasia or aplasia of the lymphatic vessels, leading to impaired lymphatic drainage. The condition is often associated with a genetic predisposition, and it is commonly inherited in an autosomal dominant pattern, as illustrated in the accompanying diagram.

Clinical Presentation[edit]

The onset of lymphedema praecox typically occurs around puberty, although it can manifest earlier or later in some cases. The primary symptom is swelling, usually in the legs, which may be accompanied by a feeling of heaviness or discomfort. Over time, the skin over the affected area may become thickened and fibrotic.

Diagnosis[edit]

Diagnosis of lymphedema praecox is primarily clinical, based on the characteristic presentation and family history. Imaging studies, such as lymphoscintigraphy, can be used to assess the function of the lymphatic system and confirm the diagnosis.

Management[edit]

Management of lymphedema praecox focuses on reducing swelling and preventing complications. This may include compression therapy, manual lymphatic drainage, and skin care to prevent infections. In some cases, surgical interventions may be considered to improve lymphatic drainage.

See also[edit]