Retroperitoneal Spindle Cell Tumor: A Case Report

Spindle cell tumor is very rare. Herein, we report a case of retroperitoneal spindle cell tumor in a 52-year-old female. The patient first presented with a complaint of persistent pain in the right upper abdomen. In the follow-up, a CT scan was performed and showed a retroperitoneal soft tissue density mass measuring 11 cm in diameter. Then, a subsequent operation was performed, and we completely removed the tumor and partially invaded lesions. The tumor was histologically diagnosed as a spindle cell tumor. Therefore, it is imperative for us to enhance the understanding of this seldom found tumor. Surgery remains the best option for treatment.

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Malignant transformation of leiomyoma of the mandible into leiomyosarcoma: A case report

Journal of Craniomaxillofacial Research ◽

10.18502/jcr.v6i4.3294 ◽

2020 ◽

Author(s):

Masoud Fallahi Motlagh ◽

Yousef Janbaz ◽

Zahra Mirzaei

Keyword(s):

Case Report ◽

Spindle Cell ◽

Neck Region ◽

Surgical Excision ◽

Metastatic Tumor ◽

Cell Tumor ◽

Spindle Cell Tumor ◽

Head And Neck Region ◽

Clinical Appearance

Lelomyosarcoma(LMS) is an uncommon malignant spindle cell tumor of the head and neck region. It is extremely rare in the oral cavity that arises from smooth muscle differentiation. It may arise as primary, radiation-associated, or metastatic tumor. The clinical appearance of these tumors can be deceptively benign and can be mistaken for non-malignant conditions. Here We present a case with atypical leiomyoma of the mandible in a 40-year- old man who referred with complaint of pain and swelling in his jaw. He underwent surgery and histology and immonohistochemestery studies confirmed the diagnosis. After 6 months recurrence occurred. Histologic examination confirmed leiomyosarcoma so he was managed with surgical excision followed by radiotherapy and chemotherapy without any recurrence or metastasis after 2 years of follow-up.

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First Experience of Ankle Joint Arthroplasty in a Giant Cell Tumor of the Tibial Epiphysiometaphys: Case Report and Literature Review

N N Priorov Journal of Traumatology and Orthopedics ◽

10.32414/0869-8678-2017-4-56-61 ◽

2017 ◽

pp. 56-61

Author(s):

A. I. Snetkov ◽

G. N. Berchenko ◽

A. R. Frantov ◽

S. Yu. Batrakov ◽

R. S. Kotlyarov ◽

...

Keyword(s):

Case Report ◽

Giant Cell Tumor ◽

Giant Cell ◽

Ankle Joint ◽

Surgical Intervention ◽

Joint Arthroplasty ◽

Cell Tumor ◽

Custom Made ◽

The Right

Case report for the 18 years old female patient with a giant cell tumor of the distal articular end of the right tibia is presented. The surgical intervention included segmental resection of the articular end of the right tibia and substitution of the defect with the custom-made ankle endoprosthesis. The follow up period made up 4 years. The range of motion in the right ankle joint was satisfactory, no relapse occurred and the implant components were stable.

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Myofibroblastoma of the Breast: Literature Review and Case Report

Case Reports in Oncological Medicine ◽

10.1155/2016/1714382 ◽

2016 ◽

Vol 2016 ◽

pp. 1-4 ◽

Cited By ~ 2

Author(s):

Mario Metry ◽

Mohamad Shaaban ◽

Magdi Youssef ◽

Michael Carr

Keyword(s):

Differential Diagnosis ◽

Case Report ◽

Literature Review ◽

Spindle Cell ◽

Cell Tumor ◽

Breast Mass ◽

Rare Tumor ◽

Spindle Cell Tumor ◽

Pathological Features

Myofibroblastoma of the breast is a rare benign spindle cell tumor. The main aim of this study is to review the literature of this rare tumor. We present a case of a mammary myofibroblastoma occurring in an 82-year-old man, emphasizing the clinical, radiological, and pathological features. The tumor was successfully identified and managed in our hospital. We would like to draw the attention of clinicians to myofibroblastoma as a rare possibility in the differential diagnosis of a breast mass.

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Spindle Cell Tumor in Oral Cavity: A Rare Case Report

International Journal of Contemporary Medicine Surgery and Radiology ◽

10.21276/ijcmsr.2018.3.4.39 ◽

2018 ◽

Vol 3 (4) ◽

Author(s):

Richa Wadhawan ◽

Nisheeth Saawarn ◽

Swati Saawarn ◽

Dharmendra Sharma

Keyword(s):

Case Report ◽

Oral Cavity ◽

Rare Case ◽

Spindle Cell ◽

Cell Tumor ◽

Spindle Cell Tumor ◽

Rare Case Report

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A rare case of spindle cell tumour of mesentery

International Surgery Journal ◽

10.18203/2349-2902.isj20212741 ◽

2021 ◽

Vol 8 (7) ◽

pp. 2216

Author(s):

Aftab S. Shaikh ◽

Amarjeet E. Tandur ◽

Ahana Ghosh ◽

Ajay H. Bhandarwar ◽

Lavina Loungani ◽

...

Keyword(s):

Rare Case ◽

Spindle Cell ◽

Iliac Fossa ◽

Previous History ◽

Cell Tumor ◽

Distal Ileum ◽

Spindle Cell Tumor ◽

Rectosigmoid Junction ◽

Neoplastic Lesion ◽

The Right

We herein reported a rare case of a patient who developed a spindle cell tumor of the mesentery. A 45 years old female with a previous history of hysterectomy presented with pain in the abdomen for two weeks. CT scan was suggestive of a well-defined solid, enhancing lesion in the right pelvic region and iliac fossa measuring 10.9×13.9×15.1 cm, abutting right ovary, ileocaecal junction, caecum, appendix and rectosigmoid junction (possible differentials) are right ovarian neoplastic lesion or desmoid tumor. The patient was planned for surgery underwent laparotomy, where the mass appeared to originate from the mesentery (15×12) in dimensions and was adherent to distal ileum and caecum. The mass was inseparable, hence, the right quadra colectomy was taken and the whole mass with distal ileum and caecum and right colon was excised and ileocolic anastomosis was done. The tumor was histologically diagnosed as a spindle cell tumor. Follow up of the patient had been uneventful.

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