29 May 2023>: Articles
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 A* , Puwitch Charoenchue B , Sunhawit Junrungsee B , Chanakrit Boonplod B , Kornkanok Sukpan DDOI: 10.12659/AJCR.939397
Am J Case Rep 2023; 24:e939397
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×).