Acquired progressive lymphangioma: Difference between revisions
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{{Infobox medical condition | |||
| name = Acquired progressive lymphangioma | |||
| synonyms = [[Benign lymphangioendothelioma]] | |||
| specialty = [[Dermatology]] | |||
| symptoms = Slow-growing, red-brown patches on the skin | |||
| onset = Any age, but often in [[adulthood]] | |||
| duration = Chronic | |||
| causes = Unknown | |||
| risks = No known risk factors | |||
| diagnosis = [[Clinical diagnosis]], [[skin biopsy]] | |||
| differential = [[Lymphangioma]], [[Kaposi's sarcoma]], [[Angiosarcoma]] | |||
| treatment = [[Surgical excision]], [[laser therapy]] | |||
| prognosis = Generally good, benign condition | |||
| frequency = Rare | |||
}} | |||
'''Acquired Progressive Lymphangioma''' (APL) is a rare [[skin disorder]] characterized by the progressive growth of [[lymphatic vessels]]. It is also known as benign lymphangioendothelioma. | '''Acquired Progressive Lymphangioma''' (APL) is a rare [[skin disorder]] characterized by the progressive growth of [[lymphatic vessels]]. It is also known as benign lymphangioendothelioma. | ||
==Etiology== | ==Etiology== | ||
The exact cause of Acquired Progressive Lymphangioma is unknown. However, it is believed to be associated with the abnormal proliferation of [[lymphatic endothelial cells]]. Some researchers suggest that it may be triggered by trauma or inflammation, but this theory is not universally accepted. | The exact cause of Acquired Progressive Lymphangioma is unknown. However, it is believed to be associated with the abnormal proliferation of [[lymphatic endothelial cells]]. Some researchers suggest that it may be triggered by trauma or inflammation, but this theory is not universally accepted. | ||
==Clinical Features== | ==Clinical Features== | ||
Acquired Progressive Lymphangioma typically presents as clusters of small, translucent, vesicle-like papules. These papules are often filled with lymph fluid and can range in color from clear to red or purple. They are usually found on the trunk or limbs and tend to grow slowly over time. | Acquired Progressive Lymphangioma typically presents as clusters of small, translucent, vesicle-like papules. These papules are often filled with lymph fluid and can range in color from clear to red or purple. They are usually found on the trunk or limbs and tend to grow slowly over time. | ||
==Diagnosis== | ==Diagnosis== | ||
Diagnosis of Acquired Progressive Lymphangioma is primarily based on clinical examination and histopathological analysis. [[Biopsy]] of the lesion can confirm the diagnosis. The histopathological features include dilated lymphatic channels in the dermis, lined by a single layer of endothelial cells. | Diagnosis of Acquired Progressive Lymphangioma is primarily based on clinical examination and histopathological analysis. [[Biopsy]] of the lesion can confirm the diagnosis. The histopathological features include dilated lymphatic channels in the dermis, lined by a single layer of endothelial cells. | ||
==Treatment== | ==Treatment== | ||
Treatment options for Acquired Progressive Lymphangioma are limited due to its rarity. Surgical excision is the most common treatment method. Other treatment options include [[laser therapy]], [[sclerotherapy]], and [[radiotherapy]]. However, recurrence after treatment is common. | Treatment options for Acquired Progressive Lymphangioma are limited due to its rarity. Surgical excision is the most common treatment method. Other treatment options include [[laser therapy]], [[sclerotherapy]], and [[radiotherapy]]. However, recurrence after treatment is common. | ||
==Prognosis== | ==Prognosis== | ||
The prognosis for Acquired Progressive Lymphangioma is generally good. Although the condition is progressive, it is benign and does not metastasize. However, it can cause significant cosmetic and psychological distress to the patient. | The prognosis for Acquired Progressive Lymphangioma is generally good. Although the condition is progressive, it is benign and does not metastasize. However, it can cause significant cosmetic and psychological distress to the patient. | ||
==See Also== | ==See Also== | ||
* [[Lymphangioma]] | * [[Lymphangioma]] | ||
* [[Lymphatic system]] | * [[Lymphatic system]] | ||
* [[Skin disorder]] | * [[Skin disorder]] | ||
[[Category:Dermatology]] | [[Category:Dermatology]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
Latest revision as of 23:28, 3 April 2025
| Acquired progressive lymphangioma | |
|---|---|
| Synonyms | Benign lymphangioendothelioma |
| Pronounce | N/A |
| Specialty | Dermatology |
| Symptoms | Slow-growing, red-brown patches on the skin |
| Complications | N/A |
| Onset | Any age, but often in adulthood |
| Duration | Chronic |
| Types | N/A |
| Causes | Unknown |
| Risks | No known risk factors |
| Diagnosis | Clinical diagnosis, skin biopsy |
| Differential diagnosis | Lymphangioma, Kaposi's sarcoma, Angiosarcoma |
| Prevention | N/A |
| Treatment | Surgical excision, laser therapy |
| Medication | N/A |
| Prognosis | Generally good, benign condition |
| Frequency | Rare |
| Deaths | N/A |
Acquired Progressive Lymphangioma (APL) is a rare skin disorder characterized by the progressive growth of lymphatic vessels. It is also known as benign lymphangioendothelioma.
Etiology[edit]
The exact cause of Acquired Progressive Lymphangioma is unknown. However, it is believed to be associated with the abnormal proliferation of lymphatic endothelial cells. Some researchers suggest that it may be triggered by trauma or inflammation, but this theory is not universally accepted.
Clinical Features[edit]
Acquired Progressive Lymphangioma typically presents as clusters of small, translucent, vesicle-like papules. These papules are often filled with lymph fluid and can range in color from clear to red or purple. They are usually found on the trunk or limbs and tend to grow slowly over time.
Diagnosis[edit]
Diagnosis of Acquired Progressive Lymphangioma is primarily based on clinical examination and histopathological analysis. Biopsy of the lesion can confirm the diagnosis. The histopathological features include dilated lymphatic channels in the dermis, lined by a single layer of endothelial cells.
Treatment[edit]
Treatment options for Acquired Progressive Lymphangioma are limited due to its rarity. Surgical excision is the most common treatment method. Other treatment options include laser therapy, sclerotherapy, and radiotherapy. However, recurrence after treatment is common.
Prognosis[edit]
The prognosis for Acquired Progressive Lymphangioma is generally good. Although the condition is progressive, it is benign and does not metastasize. However, it can cause significant cosmetic and psychological distress to the patient.
See Also[edit]
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