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Vascular Tumours

Pathology of Arteriovenous

Hemangioma

[Arteriovenous Malformation]

Dr Sampurna Roy MD

                            

 

Dermpath- India

 Site created by

 Dr Sampurna Roy MD

       

http://www.histo pathology-india.net/dermpath.htm

August  2014

 

Dr Sampurna Roy  MD

Consultant  Histopathologist (Kolkata - India)

 

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Arteriovenous hemangioma (malformations) is a benign acquired cutaneous vascular lesion and is characterized by a complex network of intercommunicating arterial and venous structures.

The etiology of arteriovenous hemangioma is uncertain; endocrine and inflammatory stimuli may activate an underlying vascular malformation. Some lesions, especially those in younger patients, may be true hamartomas.

Arteriovenous malformations grow proportionately with the patient; do not involute; and may sometimes increase in size because of vascular ectasia induced by conditions such as sepsis, trauma, puberty, and pregnancy. 

Arteriovenous hemangioma are divided into types according to  the depth of involvement:

1. Deep form:  

May be associated with arteriovenous shunting and soft tissue hypertrophy.

Age:  Young adults and adolescents.

Site: Commonly affect the head, neck and lower extremity.

Clinical presentation:  Can present with severe symptoms of heart failure or Kasabach Merritt syndrome.

This form of hemangioma may be difficult to diagnose.

Clinicopathologic correlation with arteriographic studies is essential in establishing the diagnosis.

2. Superficial form: (cirsoid aneurysm or acral arteriovenous tumour)

Age: Middle aged and elderly adults.

Site:  Usually affect the head and neck region. These are often localized to the dermis and submucosa of the lips and perioral skin.

Clinical presentation:  Small reddish blue papule. Symptoms are mild and include pain and intermittent bleeding.

Histopathological features:    

In both forms  there are thick and thin-walled sized arteries and veins in  close association with one another.

Focally, some tumours resemble capillary and cavernous hemangioma.

There may be focal thrombosis, secondary dystrophic calcification and mild inflammation.

Serial sections are helpful in demonstrating continuities or shunts between arteries and veins.

Pathologists rely on elastic stains for making a definitive diagnosis of arteriovenous malformations, because arteries and arterioles (with elastic lamina in their walls) are an integral part of Arteriovenous malformations .

These lesions grow slowly and achieve only a small size and are usually cured by simple excision.

                

 

                                            

Further reading:

Hemangioma versus vascular malformation: presence of nerve bundle is a diagnostic clue for vascular malformation.

Hemangioma and vascular malformation of small intestine: a clinicopathologic analysis of fifty-one cases. 

A study on clinical differential diagnosis between hemangioma and vascular malformation in infant

Arteriovenous haemangioma in chronic liver disease: clinical and histopathological features of four cases.

Superficial arteriovenous hemangioma of the oral cavity.

Arteriovenous hemangioma: a clinicopathological and immunohistochemical study. 

Giant arteriovenous hemangioma (cirsoid aneurysm) of the nose.

Acral arteriovenous tumor. A clinicopathologic review.

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Masson's Tumour (Intravascular papillary endothelial hyperplasia)

Acro-angiodermatitis / pseudo-Kaposi's sarcoma

Reactive angioendotheliomatosis

Infantile Hemangioma

Glomeruloid hemangioma

Acquired tufted angioma

Verrucous hemangioma

Cherry angioma/senile angioma

Microvenular hemangioma

Targetoid hemosiderotic hemangioma (Hobnail hemangioma)

Spindle cell  hemangioma / hemangioendothelioma

Kaposiform hemangioendothelioma 

Retiform hemangioendothelioma 

Papillary intralymphatic angioendothelioma (Dabska's tumour)

Composite hemangioendothelioma 

Polymorphous  hemangioendothelioma

Kaposi's sarcoma

Epithelioid hemangioendothelioma

Angiosarcoma

Glomus tumour

Hemangiopericytoma

Sinonasal Hemangiopericytoma

Lipomatous hemagiopericytoma

Myopericytoma

Angiolipoma

Aggressive angiomyxoma

Angiomyofibroblastoma

Angioleiomyoma

Angiomyolipoma

Dermatofibroma (aneurysmal variant)

Pseudoangiomatous Spindle Cell Lipoma

Kimura's disease


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