Malignant giant cell tumor of soft parts in lumbosacral region

AUTHORS

Farzaneh Jadali 1 , * , A Almasi 2 , A Gharib 3

1 Associate Professor, PIRC (Pediatric Infection Research Centre), Shahid Beheshti Medical University (MC), Mofid Hospital, Iran

2 Pathologist, Iranian Blood Transfusion Organization (IBTO), Iran

3 Assistant Professor, PIRC (Pediatric Infection Research Centre) Shahid Beheshti Medical University (MC), Mofid Hospital, Iran

How to Cite: Jadali F, Almasi A, Gharib A. Malignant giant cell tumor of soft parts in lumbosacral region, Int J Cancer Manag. 2008 ; 1(2):e80430.

ARTICLE INFORMATION

International Journal of Cancer Management: 1 (2); e80430
Published Online: April 30, 2008
Article Type: Case Report
Received: April 30, 2008
Accepted: April 30, 2008

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Abstract

Background: Giant cell tumor of soft parts is a rare neoplasm that mainly affects adulst and the elderly and is usually located in the extremities. Here we report a child with giant cell tumor of soft tissue, which is a very rare condition in childhood.

Clinical presentation: A 5 year old girl presented with a 5 month history of left lower extremity pain. She had developed paraplegia before admission. On examination, mild left lumbosacral swelling and tenderness was found. Abdominal and pelvic CT-Scan revealed an expansile lytic lesion of the left side of sacrum with significant soft tissue component extending toward the left iliac bone. Lumbar MRI revealed a space occupying lesion originating from posterior L5 elements, projecting toward the L1.

Intervention: The patient underwent surgery. A firm epidural hemorrhagic tumor of L5, S1, and S2 with no spinal cord involvement was found. Partial tumor resection (measuring 3*1*0.5 cm in maximal diameter) and laminectomy was done.

Conclusion: Primary giant cell tumors of soft tissue are distinctive, rare neoplasms that exhibit a wide clinicopathologic spectrum similar to osseous GCTs and need to be differentiated from other giant cell rich soft tissue tumors. Recognition of this tumor is important due to its behavior as a low grade malignancy, but this cannot be predicted and metastasis does occur rarely.

Keywords

Giant cell tumor of soft tissue (GCT-ST) large cell sarcoma of tendon sheath

© 2008, Author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

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