Biopsy of Bone and Soft Tissue Tumours: Hints and Hazards

2009 ◽  
pp. 3-10 ◽  
Author(s):  
Andreas Leithner ◽  
Werner Maurer-Ertl ◽  
Reinhard Windhager
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Tumours

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)

A statistical model for ultrasound diagnosis of soft-tissue tumours in the hand and forearm

1997 ◽  
Vol 38 (3) ◽  
pp. 355-358
Author(s):  
M. Hoglund ◽  
C. Muren ◽  
G. Brattstrom
Keyword(s):  
Soft Tissue ◽  
Statistical Model ◽  
Ultrasound Diagnosis ◽  
Soft Tissue Tumours

Non-neurogenic soft tissue tumours of the axilla: Prospective review of 16 cases

1989 ◽  
Vol 42 (2) ◽  
pp. 73-79 ◽  
Author(s):  
R. S. Bell ◽  
J. Ready ◽  
A. Hudson ◽  
B. O'sullivan ◽  
J. Mahoney ◽  
...  
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Tumours

SOFT-TISSUE TUMOURS

BMJ ◽  
1959 ◽  
Vol 2 (5149) ◽  
pp. 413-413
Author(s):  
B. S. Cardell
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Tumours

The management of soft tissue tumours

1978 ◽  
Vol 1 (4) ◽  
pp. 289-298 ◽  
Author(s):  
Bertil Stener
Keyword(s):  
Soft Tissue ◽  
Soft Tissue Tumours

Simultaneous double laryngeal tumours: a diagnostic and therapeutic challenge

2021 ◽  
Vol 14 (2) ◽  
pp. e239797
Author(s):  
Fergus Cooper ◽  
Rafael Moleron ◽  
Andrea Chapman ◽  
Muhammad Shakeel
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Soft Tissue ◽  
Histological Analysis ◽  
Primary Tumour ◽  
Second Primary ◽  
Soft Tissue Tumours ◽  
Rare Presentation ◽  
Laryngeal Tumours ◽  
Second Primary Tumour

Leiomyosarcomas are soft tissue tumours that rarely occur in the larynx. This case report describes the presentation and management of a 77-year-old man referred to the otolaryngology clinic with hoarseness who was found to have a large supraglottic leiomyosarcoma after panendoscopy and biopsies. He subsequently underwent laryngectomy for treatment of this tumour but, unexpectedly, the histological analysis of the laryngectomy specimen revealed a second primary tumour in the larynx—a squamous cell carcinoma (SCC). The patient had further treatment with neck radiotherapy. Three years after treatment, there are no signs of recurrence of either tumour. This case report discusses the very few similar cases of leiomyosarcoma coexisting with SCC in the larynx, collating the evidence surrounding the treatment of this rare presentation.

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