AI Article Synopsis

  • Primary cutaneous angiosarcoma is a rare and complex malignant tumor that poses challenges for diagnosis and treatment.
  • A 76-year-old man had a lump on his eyelid, initially misdiagnosed, but after biopsies and surgeries, low-grade cutaneous angiosarcoma was confirmed.
  • Despite multiple surgeries to remove the tumor, it persisted, leading the patient to choose adjuvant radiotherapy and chemotherapy instead of more surgery, highlighting the difficulties in managing this condition.

Article Abstract

Primary cutaneous angiosarcoma is a rare vasoformative malignant neoplasm that can present a diagnostic and therapeutic challenge. We describe a 76-year-old Caucasian man with right upper eyelid swelling and nodularity, initially suspected clinically to represent either ocular adnexal lymphoma or basal cell carcinoma. Incisional biopsy and wide resection of the mass with frozen section control of margins were interpreted as compatible with hobnail (Dabska-retiform) hemangioendothelioma. Foci of atypia were noted in the tumor, raising speculation of evolution into a more aggressive neoplasm, such as conventional angiosarcoma. The patient subsequently underwent two additional wide resections with frozen section control of margins in an attempt to obtain complete excision of residual tumor, which demonstrated histopathologic features favoring angiosarcoma. The histologic material from the original and subsequent resections was sent in consultation to several soft tissue pathology experts and the final diagnosis of low-grade cutaneous angiosarcoma was established. Despite repeated surgical interventions, there was continued persistence of the tumor in the deep orbital tissues. Various management options, including adjuvant radiotherapy/chemotherapy with and without orbital exenteration, were discussed. The patient decided against further surgical intervention and is currently undergoing adjuvant radiotherapy/chemotherapy. This case illustrates the diagnostic and management difficulties of ocular adnexal angiosarcoma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322085PMC
http://dx.doi.org/10.1159/000485427DOI Listing

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