• Journal of the Korean Society of Radiology
• /
• v.84 no.1
• /
• pp.275-279
• /
• 2023

Granular cell tumors (GCTs) are rare benign soft tissue tumors that can occur throughout the body, particularly the head and neck; only 5%-8% of GCTs occur in the breast. We report a case of a GCT of the axillary accessory breast, which is a rare location of this tumor. A 50-year-old woman had a 2-month history of a palpable mass in the left axilla. Physical examination, as well as mammographic and ultrasonographic findings suggested a breast malignancy. Histopathological examination showed a benign GCT, and wide local excision was performed. The patient has remained disease-free over 2 years postoperatively. Although most GCTs are benign, wide complete resection of the tumor and follow-up are required considering the possibility of recurrence. The radiologist should know the characteristics of GCTs as a differential diagnosis of breast and axillary lesions to prevent unnecessary treatment.

• Journal of the Korean Society of Radiology
• /
• v.83 no.5
• /
• pp.1195-1200
• /
• 2022

A granular cell tumor (GCT) is a rare soft tissue tumor that usually arises from the striated muscle of the tongue. Few literatures have reported pectoral muscle involvement of the GCT. Herein, we report a rare case of a GCT originating from the pectoral muscle below the breast with multimodal imaging appearance.

• Journal of Chest Surgery
• /
• v.39 no.3 s.260
• /
• pp.244-247
• /
• 2006

Granular cell tumors (GCT) are uncommon benign neoplasms. Their location is mostly in the the skin, tongue, and breast; appearance in other parts of the body is rare, but it has been reported. They have also been reported to occur synchronously in multiple organs and metachronously in a single organ. The incidence of GCTs in the tracheobronchial tree is unknown and pulmonary GCTs are uncommon, with approximately 100 reported cases in the literature. We present the case of a 33-year-old man with a granular cell tumor of the left main bronchus. The tumor was found at bronchoscopy performed to exclude suspected endobronchial mass with symptoms of pneumonia. Biopsies revealed the histological pattern of a benign granular cell tumor. He underwent resection of the left main bronchus followed by end to end anastomosis of left main bronchus. He has not had any recurrence of the tumor during the 1 year follow-up.

• 대한세포병리학회:학술대회논문집
• /
• 1993.06a
• /
• pp.22-22
• /
• 1993

• Journal of the Korean Society of Radiology
• /
• v.79 no.5
• /
• pp.259-263
• /
• 2018

A 52-year-old male complained of a painless, firm, and slow-growing mass in his right breast outer portion. The chest CT revealed a 3.3 cm-sized oval shaped, microlobulated, mild enhancing mass. Ultrasound showed a microlobulated marginated heterogeneous hypoechoic mass with internal vascularity and calcifications in the mass. On the ultrasound-guided core needle biopsy, the mass was confirmed as a benign granular cell tumor (GCT). The patient transferred to another hospital and underwent surgical removal of the lesion. GCT of the breast is uncommon and mostly benign neoplasm to originate from Schwann cell. Clinical and radiologic features of GCTs, including CT and ultrasound images, mimic malignancy and make diagnosis of GCT more difficult. The CT images of GCTs are much rarely reported. Physicians and radiologists must be aware of radiologic characteristics of this rare benign tumor for male breast, to avoid misdiagnosis this tumor for breast malignancy and overtreat.

• Korean Journal of Head & Neck Oncology
• /
• v.22 no.1
• /
• pp.43-46
• /
• 2006

Granular cell tumor is not rare and is a well recognized entity which has a wide anatomic distribution, with roughly one half of the lesions found in the head and neck. However, occurrence in the thyroid is extremely rare and has not been described well as surgeon's view. The authors have recently experienced a case of multifocal granular cell tumor of the thyroid in a 26-year-old women presented with painless mass in the anterior neck area and fatigue. So, we present this case with the review of literatures.

• Korean Journal of Head & Neck Oncology
• /
• v.25 no.2
• /
• pp.146-149
• /
• 2009

외이도의 종양은 드물며, 귀지샘에서 기원한 종양은 더욱 흔하지 않다. 저자들은 이루를 동반한 2예의 귀지샘종을 보고하고자 한다. 현미경적으로, 2예 모두 중층 혹은 단층으로 둘러싸인 세관 혹은 샘으로 이루어진 경계가 좋은 종양이었다. 종양세포는 과립성의 풍부한 호산성 세포질을 가졌고, 세포질의 관내 돌출이 관찰되어 아포크린화생을 보였다. 완전 절제후 재발은 관찰되지 않았다. 귀지샘종은 경계가 좋은 양성종양이며, 광범위 절제 치료하지만, 높은 재발율을 보인다. 여기에서 외이도에서 발생한 귀지샘종의 임상적 소견과 함께 병리 소견에 대해 기술하였다.

• Investigative Magnetic Resonance Imaging
• /
• v.13 no.1
• /
• pp.88-92
• /
• 2009

Granulocytic sarcoma is a rare extramedullary tumor composed of immature granulocytic precursors. Usually, granulocytic sarcoma is seen in association with acute myeloid leukemia, or other myeloproliferative disorders. Rarely, it may manifest as a primary presentation before the onset of systemic disease in acute myeloid leukemia. The clinical suspicion of granulocytic sarcoma based on imaging findings is important for the management of the patient especially when systemic disease of acute myeloid leukemia is not confirmed as in our case. We report the MR findings of a granulocytic sarcoma in the left leg mimicking hemorrhagic abscess in a patient with acute myeloid leukemia. We believe that MRI can be a helpful diagnostic method of making a differential diagnosis of granulocytic sarcoma in a patient with leukemia, and this can be done by analyzing the signal intensity and the enhancement pattern.

• Tuberculosis and Respiratory Diseases
• /
• v.48 no.1
• /
• pp.96-102
• /
• 2000

Granular Cell Tumors(GCT) were originally described as myoblastic myomas. This tumor is believed to originate from Schwann cells based on subsequent scientific investigations. Although it usually appears in the head and neck, it can also appear in other organs as well. Endobronchial granular cell tumors are rather rare and should be differentiated from other common endobronchial diseases such as bronchogenic carcinoma and endobronchial tuberculosis, especially. A case of a patient with an extremely rare condition of endobronchial granular cell tumor concurrent with malignant mediastinal tumor is reported.

• Journal of the Korean Society of Laryngology, Phoniatrics and Logopedics
• /
• v.31 no.1
• /
• pp.45-48
• /
• 2020

Granular cell tumor is rare tumor origination from Schwann cell. It occurs extremely rarely in pediatric age. Treatment is complete resection, but this may not always be possible because of the risk of airway stenosis or vocal cord paralysis. Six year-old male patient visited otolaryngology clinic due to dyspnea and stridor. Posterior glottis mass was indentified and was partially resected to confirm histology and resolve airway obstruction. One year after operation, the patient was living well without re-growing of tumor. We report a case of granular cell tumor in pediatric larynx with a review of literature.