Сutaneous angiosarcoma

Angiosarcoma (AS) is an uncommon malignant neoplasm characterized by rapidly proliferating, extensively infiltrating anaplastic cells derived from blood vessels. These are aggressive tumors and tend to recur locally, spread widely with high rate of lymph node and systemic metastases. They are more frequent in skin and soft tissue, head and neck being the most common sites. Here we report a case of metastatic AS affecting lower extremity in an young patient on a background of chronic lymphedema.


Case Report

A 28-year-old man with chronic lymphedema in the left lower extremity and the scrotum for 12 years presented with a multiple nodules on left leg. PET images at baseline reveal multiple 18F-FDG avid lesions in the left leg associated with lytic metastasis to the left sacrum and with spleen metastasis. Patient had received treatment with adriamycin and olaratumab without significant improvement.


AS is a rare and aggressive malignant tumor of vascular endothelial origin comprising approximately 2% of soft tissue sarcomas. Among all cases of AS, one third occurs in the skin, one fourth in soft tissue, and the remainder in other sites.

Due to variable clinical scenarios that may be associated with this tumor, different presentations are seen, for example, lymphedema-associated AS, radiation-induced AS, primary breast AS, AS of the soft tissue, and cutaneous angiosarcoma (CA). Factors that have been implicated in the pathogenesis of this tumor include radiation, lymphedema, vascular insufficiency, ulceration, and chemicals such as vinyl chloride, arsenic, and thorium dioxide. However, approximately 78–95% of CA arise with no predisposing factors. CA usually affects the head and the neck (with scalp involvement in 50% of cases), they are infrequent in the lower extremity. CA occurs most often in patients over the age of 60, with a M/F sex ratio of 2.5 to 3:1.

Clinically, CAs usually present as nodules or angiomatous, erythematous, and purplish plaques, which may be confused with hematoma, hemangioma, localized inflammatory edema, rhinophyma, purpuric patches, keratotic lesions, verrucous lesions, Kaposi sarcoma (multiple hemorrhagic sarcoma), Kaposi-like hemangioendothelioma, angiolymphoid hyperplasia, Kimura’s disease, amelanotic melanoma or pyogenic granuloma. AS arising in an area of chronic lymphedema is referred to as STS. Stewart and Treves first described lymphangiosarcoma occurring in post-mastectomy lymphedema of the arm in 1948. AS arising in a chronically lymphedematous leg is rare.

In the majority of patients, the AS is relatively large (at least 10 cm in diameter) at the time of presentation because of a significant delay in diagnosis. The incidence of STS is low. The prevalence has been estimated at between 0.45% and 0.07% of patients treated for early carcinoma of the breast. STS in the lower extremity is reported only occasionally. STS typically develops after 10–15 years latency and accounts for approximately 5% of ASs.

The accumulation of protein rich interstitial fluid alters the local immune response within the affected limb and stimulates lymphangiogenesis for the development of collateral vessels. Because immune surveillance is compromised, lymphedema creates an immunologically vulnerable milieu for the development of malignancy, specifically vascular tumors.

The histologic findings of AS in STS show a proliferation of irregular anastomosing vascular channels that dissect dermal collagen. The malignant endothelial cells lining these channels are hyperchromatic and pleomorphic with large nucleoli and frequent mitosis. The tumor cells are round to ovoid with a predominantly epithelioid and spindle-shaped morphology. Overlying epidermis may be acanthotic, hyperkeratotic, or atrophic, with or without proliferation of reticular fibers in the dermis. A large percentage of ASs stain positive for CD31 and CD34, of which, CD31 is the more sensitive and specific of the two. Cytokeratin stains may be positive in some epithelioid ASs.

Histopathologically, early lesions of CAS should be differentiated from benign vascular proliferation and Kaposi’s sarcoma.

Differentiation from benign vascular proliferations depends on recognition of cellular atypia, presence of crowding of lining cells and of solid papillary clusters of cells, and irregular interconnecting pattern of vessels. There is strong expression of mitogen activated protein kinase (MAPK) in benign endothelial tumors and greatly decreased expression in AS.

Kaposi’s sarcoma is characterized by spindle cell proliferation with mild nuclear atypia, low mitotic activity, vascular slits, and extravasated RBCs. The tumor tends to grow around large vessels and follow lymphangitic distribution. The tumor cells show moderate to diffuse positivity for CD31, CD34, and Human Herpes Virus (HHV)-8.

AS on the other hand is characterized by a proliferation of atypical cells lining anastomosing vessels that strongly react with vascular endothelial markers such as factor VIII-related antigen, CD31, and CD 34.

Treatment depends upon the general health of the patient, tumor location, histologic subtype, and extent of involvement. Localized and advanced cutaneous disease is frequently treated similarly with neoadjuvant chemotherapy followed by wide local excision or amputation and radiation therapy. Additional therapeutic options for locally advanced disease include the use of loco-regional modalities such as isolated limb perfusion, limb infusion, and electrochemotherapy.

Prognosis of CA is poor regardless of subtype and treatment offered. Depending on the modality of treatment, local recurrences have been observed in 35–86% of cases. The proclivity for distant pulmonary metastases has been well-documented.[14] Survival rates range from 51% at 5 years to 43% at 10 years. Patients with localized disease have a better overall outcome with 5- and 10-year survival rates of 62% and 54%, respectively. Those with distant metastasis have a 6.2% chance of survival at both 5 and 10 years.


Tambe SA, Chitra S. Nayak CS. Metastatic Angiosarcoma of Lower Extremity. Indian Dermatol Online J. 2018 May-Jun; 9(3): 177–181.

Posted on 13.05.19

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