Published online Nov 26, 2023. doi: 10.12998/wjcc.v11.i33.8044
Peer-review started: August 21, 2023
First decision: August 30, 2023
Revised: September 26, 2023
Accepted: November 13, 2023
Article in press: November 13, 2023
Published online: November 26, 2023
Processing time: 94 Days and 18.3 Hours
Granular cell tumor (GCT) of the breast (GCTB) is a rare neoplasm that can exhibit malignant characteristics both clinically and radiologically. This tumor can also coexist and colocalize with breast carcinoma.
We present a patient with this uncommon tumor and discuss the diagnostic and therapeutic approaches in order to further the knowledge of GCTB and prevent misdiagnosis and overtreatment. The characteristics of the tumor, methods of diagnosis, therapy and postoperative pathological outcomes were analyzed, and relevant literatures of GCTs were reviewed. The patient underwent surgery after core needle biopsy, and the excised neoplasm was sent for pathological examination. Histological analysis revealed nests of cells with abundant pink granular cytoplasm, confirming the diagnosis of GCTB.
As manifestations of GCT and malignancy can mimic each other, a careful histological examination is essential before major surgery. Treatment consisting of complete excision with close clinical follow-up is recommended.
Core Tip: Granular cell tumor of the breast is a rare neoplasm that can exhibit malignant characteristics both clinically and radiologically. This tumor can also coexist and colocalize with breast carcinoma. This could result in the potential misdiagnosis of breast carcinoma and overtreatment of patients. We report a patient with this tumor and discuss the methods of diagnosis and treatment. As manifestations of the disease and malignancy can mimic each other, a careful histological examination is essential before major surgery. Complete excision with close clinical follow-up is recommended.