Journal List > Ann Dermatol > v.29(6) > 1096688

Moon, Eun, Jang, Lee, Kim, and Lee: Primary Angiosarcoma of the Skin Presenting as Mild Erythema
Dear Editor:
An 83-year-old man presented with a 3-month history of asymptomatic, ill-demarcated, mild erythema on the left zygomatic area (Fig. 1). He had no remarkable family or personal medical history. He had previously been prescribed oral dermatological medication from a private clinic, which he took for 1 month. Despite treatment, the lesion progressively increased in size. Non-specific mild erythema or early-stage erysipelas was suspected. Complete blood cell counts, basic biochemistry results, and inflammatory marker levels were within normal limits. Furthermore, bacterial cultures revealed no growth. Histopathological findings indicated proliferation of atypical endothelial cells with a network of irregular anastomosing vessels, consistent with angiosarcoma (Fig. 2A, B, C). On immunohistochemical staining, endothelial cells stained for CD31, and lymphatic endothelial cells stained for D2-40 and Prox-1 (Fig. 2D, E, F). Regional lymph node involvement or distant metastasis was not observed on computed tomography of the chest and orbit. The patient underwent six sessions of radiotherapy at 1-week intervals, and the tumor regressed.
Angiosarcoma is a rare, aggressive neoplasm of vascular endothelial cells1. In addition to primary angiosarcoma, there are two other variants: post-radiation angiosarcoma and angiosarcoma in areas of chronic lymphedema. Initially, primary angiosarcoma of the skin presents as solitary or multiple purpuric patches on the face, neck, or scalp. Early lesions can be confused with other skin lesions, such as bruises2, salmon patches, hemangiomas, hematomas3, rosacea4, rhinophyma5, and early Kaposi's sarcoma. The patient in this case exhibited a unique clinical feature, in that he presented with mild erythema rather than with angiosarcoma. Histopathology and immunohistochemical staining revealed collagen-dissecting atypical vascular proliferation, consistent with angiosarcoma. It can be challenging to diagnose mild erythema as angiosarcoma, so we emphasize the need to consider malignancy in the differential diagnosis of prolonged mild erythema.

Figures and Tables

Fig. 1

(A, B) Ill-demarcated, indurated erythema in the left zygomatic area.

ad-29-809-g001
Fig. 2

An irregular anastomosing vascular space lined with atypical endothelial cells (H&E; A: ×40, B: ×100, C: ×200). Immunohistochemical analysis of the lesion shows tumor cells stained for (D) CD31, (E) D2-40, or (F) Prox-1. D~F: ×100.

ad-29-809-g002

Notes

CONFLICTS OF INTEREST The authors have nothing to disclose.

References

1. Guadagnolo BA, Zagars GK, Araujo D, Ravi V, Shellenberger TD, Sturgis EM. Outcomes after definitive treatment for cutaneous angiosarcoma of the face and scalp. Head Neck. 2011; 33:661–667.
crossref
2. Kim JE, Kim BJ, Kang H. A recurrent angiosarcoma isolated to the eyelid without the recurrence on the primary lesion of the forehead. Ann Dermatol. 2014; 26:231–235.
crossref
3. Lemanski N, Farber M, Carruth BP, Wladis EJ. Primary adnexal angiosarcoma masquerading as periorbital hematoma. Surv Ophthalmol. 2014; 59:655–659.
4. Mentzel T, Kutzner H, Wollina U. Cutaneous angiosarcoma of the face: clinicopathologic and immunohistochemical study of a case resembling rosacea clinically. J Am Acad Dermatol. 1998; 38:837–840.
crossref
5. Aguila LI, Sánchez JL. Angiosarcoma of the face resembling rhinophyma. J Am Acad Dermatol. 2003; 49:530–531.
crossref
TOOLS
Similar articles