scholarly journals Low Grade Myofibroblastic Sarcoma in Pre-Existing Fibroadenoma – A Rare Case Report

2016 ◽  
Vol 15 (08) ◽  
pp. 123-125
Author(s):  
Dr. Abhishek Verma ◽  
Dr. Ravi Murmu ◽  
Dr. Somya Sinha ◽  
Dr. Anu Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Low Grade ◽  
Myofibroblastic Sarcoma ◽  
Rare Case Report

Primary low-grade myofibroblastic sarcoma: A rare case report of this tumor in the orbit and literature review

2020 ◽  
pp. 112067212097039
Author(s):  
Lijuan Tang ◽  
Hua Xu ◽  
Huanhuan Gao ◽  
Huasheng Yang ◽  
Shuxia Chen ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
World Health ◽  
Low Grade ◽  
Distinct Entity ◽  
Myofibroblastic Sarcoma ◽  
The World ◽  
Rare Case Report ◽  
Health Organization ◽  
Myofibroblastic Differentiation

Low-grade myofibroblastic sarcoma (LGMS) is an exceedingly rare, malignant tumor with myofibroblastic differentiation. It frequently occurs in the oral cavity and extremities, despite being classified as a distinct entity by the World Health Organization (WHO). Here, we report a rare case of orbital LGMS occurring in an 11-month-old baby with a 3.2 × 2.4 × 2.1 cm mass. LGMS was diagnosed based on the histological and immunohistochemical findings. Previous literature suggests that surgical resection with clear margins is an appropriate method for the treatment of LGMS, and combined adjuvant therapy (local radiotherapy with or without chemotherapy) can improve the prognosis, but further studies are needed.

scholarly journals Low-Grade Endometrial Stromal Sarcoma in a 22-Year-Old Maiden Female: A Rare Case Report from Syria

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Lana Nseir ◽  
Georget Mansour ◽  
Junior Makhoul ◽  
Luna Skaf ◽  
Mohammad Ziad Dahhan ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Treatment Plan ◽  
Endometrial Stromal Sarcoma ◽  
Abnormal Uterine Bleeding ◽  
Low Grade ◽  
Stromal Sarcoma ◽  
Rapid Enlargement ◽  
Rare Case Report ◽  
Immunohistochemical Studies

Endometrial stromal sarcoma (ESS) is a rare and challenging type of endometrial tumor, constituting only about 0.2% of all uterine malignancies and occurring in women 42–58 years of age. ESS is usually misdiagnosed as leiomyoma. They both have nonspecific symptoms, which makes the diagnosis of ESS difficult to achieve. As the ESS is infrequently encountered, optimal management is quite debatable. Here, we report a rare case of a 22-year-old Syrian female who presented with abnormal uterine bleeding; the preoperative diagnosis suggested leiomyoma while histopathological and immunohistochemical studies confirmed the diagnosis of LG-ESS stage IIA. Therefore, the treatment plan was shifted from a conservative myomectomy to a total hysterectomy with both adnexa. The aim of this case report is to draw attention to this uncommon tumor at young age of patients as well as to have awareness of the necessity to suspect this diagnosis especially with the presentation of rapid enlargement of uterine leiomyoma.

A Rare Case Report of Primary Low-Grade Endometrial Stromal Sarcoma (LGESS) of Ovary Infiltrating Bladder

2016 ◽  
Vol 14 (3) ◽  
Author(s):  
Senthil Kumar Ravichander ◽  
Ajay Krishna Boralkar ◽  
Neha Deepak Borde ◽  
Amol Rangnath Jadhav ◽  
Jyothi Sachin Mukhedkar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Endometrial Stromal Sarcoma ◽  
Low Grade ◽  
Stromal Sarcoma ◽  
Rare Case Report

scholarly journals A maxillary ameloblastic fibrosarcoma tumor: a rare case report from Syria

2020 ◽  
Vol 2020 (8) ◽  
Author(s):  
Amjad Soltany ◽  
Ghazal Asaad ◽  
Rami Daher ◽  
Mouhannad Dayoub ◽  
Ali Khalil ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Soft Tissue Sarcomas ◽  
Surgical Excision ◽  
Low Grade ◽  
Rare Case Report ◽  
Ameloblastic Fibrosarcoma ◽  
The Right

Abstract Ameloblastic fibrosarcoma (AFS) is a rare, aggressive malignant odontogenic tumor. AFS is seen most frequently in second and third decades of life. We are reporting a case of a low grade AFS in a 21-year-old male complaining of a painless swelling in the right side of the maxilla. The patient was treated with surgical excision followed by radiotherapy, which is considered the most effective approach for most of soft tissue sarcomas. AFS has a high-reported recurrence rate (up to 37%); therefore, long-term surveillance for recurrence is crucial.

scholarly journals Low-grade central osteosarcoma of the mandible clinically mimicking a benign fibro-osseous lesion: A rare case report

2020 ◽  
Vol 6 (1) ◽  
Author(s):  
James P. Arnold ◽  
Christopher J. Smith ◽  
Karen E. González Torres ◽  
Andrew C. Jenzer
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Low Grade ◽  
Osseous Lesion ◽  
Rare Case Report

scholarly journals Bladder Chondrosarcoma in A Male: A Rare Case Report

2021 ◽  
Vol 57 (3) ◽  
pp. 256
Author(s):  
Muhammad Husni Tamrin ◽  
Wahjoe Djatisoesanto
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Sarcoma ◽  
Rare Variant ◽  
Rare Case ◽  
Bladder Tumor ◽  
Histopathological Examination ◽  
Low Grade ◽  
Lower Abdomen ◽  
Rare Case Report

Chondrosarcoma is a rare variant of bladder tumor and one of the rare types of soft tissue sarcoma. This case happened on a 36-year-old male who complained of lumps in his lower abdomen, accompanied by difficulties in passing urine and painful urination, without hematuria. We performed TURBT and histopathological examination showed low-grade chondrosarcoma. The patient was diagnosed with low-grade bladder chondrosarcoma. The patient was treated for chemotherapy and radiotherapy. However, after undergoing one cycle of chemotherapy, the patient refused to continue the therapy.

Unicystic variant of low grade mucoepidermoid carcinoma: A rare case report

2014 ◽  
Vol 1 (2) ◽  
pp. 50-52
Author(s):  
R. Surekha ◽  
Vanishree ◽  
Dinesh Singh Chauhan ◽  
Balram Singh Thakur
Keyword(s):  
Case Report ◽  
Mucoepidermoid Carcinoma ◽  
Rare Case ◽  
Low Grade ◽  
Rare Case Report
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