scholarly journals A rare case of spindle cell tumour of mesentery

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.

scholarly journals Spindle Cell Tumor in Oral Cavity: A Rare Case Report

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

scholarly journals Retroperitoneal Spindle Cell Tumor: A Case Report

2021 ◽  
Vol 8 ◽  
Author(s):  
Hao Hua ◽  
Zhiwei He ◽  
Linhan Lei ◽  
Huahua Xie ◽  
Zilei Deng ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Spindle Cell ◽  
Cell Tumor ◽  
Tumor Surgery ◽  
Spindle Cell Tumor ◽  
Soft Tissue Density ◽  
The Right ◽  
Upper Abdomen

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.

Laparoscopic Liver Resection of a Desmoplastic Nested Spindle Cell Tumor of the Liver

2010 ◽  
Vol 76 (9) ◽  
pp. 184-185
Author(s):  
Caridad Marín ◽  
Ricardo Robles ◽  
Matilde Fuster ◽  
Pascual Parrilla
Keyword(s):  
Liver Resection ◽  
Laparoscopic Liver Resection ◽  
Spindle Cell ◽  
Cell Tumor ◽  
Spindle Cell Tumor

Hyalinizing spindle cell tumor with giant rosettes of the omentum

2003 ◽  
Vol 29 (6) ◽  
pp. 388-391 ◽  
Author(s):  
Asako Koishi ◽  
Hideto Gomibuchi ◽  
Jun Inoue ◽  
Shigeki Minoura ◽  
Eisaku Itoh ◽  
...  
Keyword(s):  
Spindle Cell ◽  
Cell Tumor ◽  
Spindle Cell Tumor

scholarly journals Aggressive Monophasic Sarcomatoid Carcinoma of Small Intestine - A Rare Case Report With Review of Literature

2012 ◽  
Vol 02 (01) ◽  
pp. 45-47
Author(s):  
Shetty K. Padma ◽  
Harish S. Permi ◽  
C.N. Patil ◽  
Michelle Mathias
Keyword(s):  
Small Intestine ◽  
Rare Case ◽  
Spindle Cell ◽  
Correct Diagnosis ◽  
Sarcomatoid Carcinoma ◽  
Intestinal Wall ◽  
Cell Tumor ◽  
Review Of Literature ◽  
Spindle Cells ◽  
Rare Case Report

AbstractSarcomatoid carcinoma occurring in the small intestine is very rare. They can be monophasic or biphasic. We report a rare case of monophasic Sarcomatoid carcinoma of the small intestine in a 60 year old male patient. The tumor was an ulceronodular mass involving the ileum circumferentially. The tumor infiltrated the full thickness of the intestinal wall and the serosa of an adjacent loop of ileum. Microscopically, the tumor was composed of sheets of malignant spindle cells. The carcinomatous nature of the tumor was evident only after Immunohistochemistry. The diagnosis of sarcomatoid carcinoma should be considered in the differential diagnosis of malignant spindle cell tumor of small intestine and immunohistochemical stains are required for the correct diagnosis.

scholarly journals Giant Cell Tumor of Bone: A rare uncommon manifestation implicated in a new mosaic of desorders?

2021 ◽  
Author(s):  
Eliandro de Souza Freitas ◽  
Francisco Amadis Batista Ferreira ◽  
Brendo Vinícius Rodrigues Louredo ◽  
Milena Gomes Melo Leite ◽  
José da Cruz Luna Neto ◽  
...  
Keyword(s):  
Maxillary Sinus ◽  
Giant Cell Tumor ◽  
Giant Cell ◽  
Rare Case ◽  
Benign Neoplasm ◽  
Cell Tumor ◽  
Long Bones ◽  
The Right

Giant Cell Tumor of Bone is an uncommon aggressive benign neoplasm that frequently affecting the epiphysis of long bones especially around the knee. This is a singular rare case of GCTB in the right maxillary sinus implicated in a process coincidentally or casually with another type of lesion primarily developed.

scholarly journals Malignant Spindle Cell Tumor Breast—a Diagnostic Dilemma

2018 ◽  
Vol 9 (3) ◽  
pp. 387-390 ◽  
Author(s):  
Sheetal Arora ◽  
Deepshikha Rana ◽  
Mukta Pujani ◽  
Varsha Chauhan
Keyword(s):  
Spindle Cell ◽  
Cell Tumor ◽  
Spindle Cell Tumor ◽  
Diagnostic Dilemma

Hyalinizing Spindle Cell Tumor With Giant Rosettes—A Soft Tissue Tumor With Mesenchymal and Neuroendocrine Features

2000 ◽  
Vol 124 (8) ◽  
pp. 1179-1184 ◽  
Author(s):  
Pablo A. Bejarano ◽  
Tapan A. Padhya ◽  
Roger Smith ◽  
Ruthann Blough ◽  
James J. Devitt ◽  
...  
Keyword(s):  
Soft Tissues ◽  
Spindle Cell ◽  
S100 Protein ◽  
Neuron Specific Enolase ◽  
Neuroendocrine Differentiation ◽  
Cell Tumor ◽  
Factor Xiiia ◽  
Spindle Cell Tumor ◽  
Balanced Translocation ◽  
Spindle Cell Proliferation

Abstract Context.—Hyalinizing spindle cell tumor with giant rosettes is a recently described biphasic neoplasm of soft tissues that shares mesenchymal and neuroendocrine features. Its morphologic structure is distinctive, with the presence of hyalinized paucicellular foci that are termed rosettes. The cells around the latter display positive immunoreactivity for neuroendocrine markers. The small number of cases described to date indicates that they tend to be localized in the extremities. Objective.—To describe the clinicopathologic features of 2 unusual cases of hyalinizing spindle cell tumor with giant rosettes. Methods and Results.—One tumor was located in the prestyloid parapharyngeal space and the second in the left thigh. Both tumors were well circumscribed and surrounded by a thin capsulelike fibrous band without infiltrating projections. The rosettes were embedded in a spindle cell proliferation. Immunohistochemical stains showed positive results for S100 protein, synaptophysin, CD57, protein gene product 9.5, and neuron-specific enolase exclusively in the cells palisading the rosettes. These markers were negative in the spindle cell portions of the tumor. The latter were immunoreactive for factor XIIIa, vimentin, HAM56, collagen IV, and CD68. Vimentin was the only marker shared by the rosette-forming cells and the spindle cells. Ultrastructurally, the rosette-forming cells contained neurosecretory granules. This study describes the first cytogenetic analysis in this type of tumor revealing 2 cell lines, both containing a balanced translocation between chromosomes 7 and 16. Follow-up of the patients at 16 and 8 months did not disclose evidence of recurrence. Conclusions.—These 2 new cases increase the awareness of hyalinizing spindle cell tumor with giant rosettes and demonstrate that it is a spindle cell neoplasm of unique cytogenetic rearrangements composed of dendritic, histiocytic, and fibroblastic cells admixed with cells that have neuroendocrine differentiation.

S100 and CD34 positive spindle cell tumor with prominent perivascular hyalinization and a novel NCOA4‐RET fusion

2019 ◽  
Author(s):  
Michael Michal ◽  
Nikola Ptáková ◽  
Petr Martínek ◽  
Zoran Gatalica ◽  
Dmitry V. Kazakov ◽  
...  
Keyword(s):  
Spindle Cell ◽  
Cell Tumor ◽  
Spindle Cell Tumor
Sign in / Sign up

Export Citation Format

Share Document