Spindle cell oncocytoma of the adenohypophysis: Report of a case with a 16-year follow-up

2006 ◽  
Vol 202 (10) ◽  
pp. 745-750 ◽  
Author(s):  
Istvan Vajtai ◽  
Rahel Sahli ◽  
Andreas Kappeler
Keyword(s):  
Spindle Cell ◽  
Spindle Cell Oncocytoma

Inflammatory Myofibroblastic Tumour in Antimesenteric Border of Descending Colon of Children: A Case Report

2015 ◽  
Vol 3 (1) ◽  
pp. 47-50
Author(s):  
Shahnoor Islam ◽  
AKM Amirul Morshed ◽  
Afiqul Islam
Keyword(s):  
Soft Tissue ◽  
Spindle Cell ◽  
Inflammatory Myofibroblastic Tumour ◽  
Pathological Findings ◽  
Soft Tissue Lesion ◽  
Soft Tissue Tumours ◽  
Inflammatory Pseudotumour ◽  
Erythrocyte Sedimentation ◽  
Antimesenteric Border

Inflammatory myofibroblastic tumour (IMT) occurring at intraabdominal sites in children has rarely been described. Inflammatory pseudotumour is a soft tissue lesion that may be confused with a sarcoma. It is abbreviated as IMT. Inflammatory myofibroblastic tumour, also known as soft tissue tumours, atypical fibromyxoid tumours, pseudosarcomatous fibromyxoid tumour, plasma cell granuloma, pseudosarcomatous myofibrotic proliferation, post-operative spindle cell nodules. In this paper, we describe a case of inflammatory myofibroblastic tumour (IMT) with an unusual constellation of clinical, pathological findings. A 10-year-old girl had an 7-cm intraabdominal mass accompanied by severe anemia, fever, constipation, weight loss, thrombocytosis, elevated erythrocyte sedimentation rate. Laparotomy was performed. The final pathologic diagnosis was IMT. At the most recent follow up (12months) after excision of the tumour, the patient was symptom-free and there was no evidence of tumour recurrence.J. Paediatr. Surg. Bangladesh 3(1): 47-50, 2012 (January)

Spindle cell oncocytoma of adenohypophysis: report of a rare pituitary tumor

2017 ◽  
Author(s):  
Carlos Marques Pontinha ◽  
Manuela Mafra ◽  
Luis Cerqueira ◽  
Amets Sagarribay ◽  
Fernando Fonseca ◽  
...  
Keyword(s):  
Pituitary Tumor ◽  
Spindle Cell ◽  
Spindle Cell Oncocytoma

Differentially expressed miRNAs in spindle cell oncocytoma of the pituitary gland

2019 ◽  
Author(s):  
Lilla Krokker ◽  
Gabor Nyirő ◽  
Lilla Reininger ◽  
Otto Darvasi ◽  
Nikolette Szucs ◽  
...  
Keyword(s):  
Pituitary Gland ◽  
Spindle Cell ◽  
Differentially Expressed ◽  
Differentially Expressed Mirnas ◽  
Spindle Cell Oncocytoma

Spindle Cell Oncocytoma

2016 ◽  
pp. 355-358
Author(s):  
Gabriel Zada ◽  
M. Beatriz S. Lopes ◽  
Srinivasan Mukundan ◽  
Edward Laws
Keyword(s):  
Spindle Cell ◽  
Spindle Cell Oncocytoma

scholarly journals Manifestation of Pleomorphic Undifferentiated Aortic Sarcoma with Splenic Infarction: A Case Report

2020 ◽  
Vol 13 (2) ◽  
pp. 1002-1005
Author(s):  
Varun Kaushal ◽  
Behzad Amoozgar ◽  
Nabonita Barua ◽  
Shankar Chhetri ◽  
Bhaveshkumar Garsondiya
Keyword(s):  
Poor Prognosis ◽  
Spindle Cell ◽  
Tumor Resection ◽  
Splenic Infarction ◽  
Spindle Cell Sarcoma ◽  
Shortness Of Breath ◽  
Major Vein ◽  
Aortic Sarcoma ◽  
Ct And Mri

Aortic spindle cell sarcoma is a rare neoplasm with poor prognosis that is often found incidentally due to its adverse effects. CT and MRI with contrast are useful imaging modalities, but a tissue biopsy is the gold standard for diagnosis. Tumor resection is the ultimate treatment followed by chemotherapy. Our case was an adult female who presented mainly for shortness of breath, and further imaging workup demonstrated a soft tumor juxtaposed to a major vein with compressive effect. The patient’s tumor was resected, and the pathology result confirmed undifferentiated aortic sarcoma. The patient’s condition improved and she was discharged with outpatient oncology follow-up and possible treatment.

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