A Rare Case of Primary Adrenal Epithelioid Angiosarcoma

Komson Wannasai; Puwitch Charoenchue; Sunhawit Junrungsee; Chanakrit Boonplod; Kornkanok Sukpan

doi:10.12659/AJCR.939397

29 May 2023 : Case report Thailand

A Rare Case of Primary Adrenal Epithelioid Angiosarcoma

Challenging differential diagnosis, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)

Komson Wannasai

^1ABCDEFG*, Puwitch Charoenchue

^2BDF, Sunhawit Junrungsee^3B, Chanakrit Boonplod

^4BEF, Kornkanok Sukpan^1D

DOI: 10.12659/AJCR.939397

Am J Case Rep 2023; 24:e939397

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Background Case Report Discussion Conclusions References:

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Figure 4. Histopathology of the adrenal gland tumor. (A) Low magnification reveals a highly cellular tumor with vascular channels (hematoxylin and eosin [H&E] 40×). (B) Medium magnification reveals tumor cells with epithelioid and spindle shapes (H&E 100×). (C) High magnification reveals pleomorphic epithelioid tumor cells with hyperchromatic nuclei, prominent nucleoli, and vesicular chromatin (H&E 400×). (D) High magnification reveals pleomorphic spindle-shaped tumor cells with hyperchromatic nuclei, prominent nucleoli, and vesicular chromatin (H&E 400×).

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A Rare Case of Primary Adrenal Epithelioid Angiosarcoma

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