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International Research Journal      ISSN-0975-3486       VOL. I * ISSUE—3&4         RNI : RAJBIL/2009/30097

                                     Research Paper—Medical
                                     SYNOVIAL SARCOMA : AN
                                    UNCOMMON CAUSE OF LEG
                                           SWELLING
                                      *Dr. Vipul Gurjar **Dr. R.P. Bharaney
 Dec.-09—Jan.-2010                           [ M.S.]                  [M.S.]
            *General Surgeon, Asst. Prof. S.B.K.S. Medical College, Pipariya
          **General Surgeon, Prof.& Head, S.B.K.S. Medical College, Pipariya
 A B S T R A C T
   Synovial sarcoma is known as soft tissue sarcoma and it is a rare form of cancer which
   usually occurs near the joints of the limbs. Here we are presenting a case of young male
   having leg lump which was investigated and operated for wide excision and later on he
   advised for post operative above knee amputation and Chemo-Radiotherapy as the
   histopathology of tumour showed poorly differentiated cells.

KEYWORDS— soft tissue leg swelling ; malignant tumour ; synovial sarcoma.
INTRODUCTION:                                             excision of lump. Histopathology showed poorly
Synovial sarcomas are malignant tumours of non-           differentiated cells. Later, patient was given advice for
epithelial extra skeletal tissue of the body and it       above knee amputation and chemo – radiotherapy .
accounts for 8% of all soft tissue sarcoma. Primary
synovial sarcoma occurs most commonly in the soft
tissue near larger joints of limbs but it may involve
most human tissue and organs like Brain, Heart and
Prostate. These tumours are rare with an annual
incidence of around 2-3 /100000 they account for less
than 1% of all malignant tumours and 2% of all cancer
related death, although in children soft tissue sarcoma
represent about 8% of all malignancy. It mainly occurs
in 3 rd decades of life of young males. [1,2].
CASE REPORT:
     A 22 year old male patient presented with a
swelling in upper leg. On examination there was a 6×6
cm, globular, firm swelling near popliteal fossa with
normal peripheral pulsation. X-ray of leg showed soft
tissue swelling & the bones were normal. Other routine
investigations like blood count, chest x-ray, USG
                                                                          FIG:1: LEG LUMP
abdomen were normal. Patient was operated for wide

çÚUâ¿ü °ÙæçÜçââ °‡ÇU §ßñËØé°àæÙ                                                                                  1
International Research Journal         ISSN-0975-3486          VOL. I * ISSUE—3 &4          RNI : RAJBIL/2009/30097
                      FIG:2:EXCISED MASS                                       DISCUSSION:
                                                                                     The pathogenesis and risk factors
                                                                               of synovial sarcoma are still unknown
                                                                               though the cells of it have a
                                                                               microscopic appearance similar to that
                                                                               of the synovium giving the disease its
                                                                               name [2]. Two cell types can be seen
                                                                               microscopically, first is fibrous type or
                                                                               spindle cell and the second is epithelial
                                                                               in appearance. The classical Synovial
                                                                               sarcoma has a biphasic appearance
                                                                               with both types present. In poorly
                                                                               differentiated or monophasic variety it
                                                                               consists only of sheets of spindle cells
                                                                               [3]. In more than 80 % of synovial
                                                                               sarcoma the translocation t(x;18) (p
                                                                               11;q 11) is seen [4]. Surgical wide
                                                                               excision is an important treatment of
          FIG:3: HISTOPATHOLOGY (REF. NO-5)                                    synovial sarcoma. A tumor free margin
                                                                               of 1-3 cm. is recommended. But when
                                                                               tumor involves neurovascular or
                                                                               deeper plane and the tumour is large
                                                                               enough more than 5cm in size then
                                                                               amputation is the surgery of choice [1,
                                                                               2, 5]. Adjuvant chemotherapy and
                                                                               neoadjuvant chemotherapy have been
                                                                               proposed for patient with metastatic
                                                                               soft tissue sarcoma [5]. Radiotherapy
                                                                               plays a well defined role in local control
                                                                               of disease as well as when tumour size
                                                                               is large [5]. Synovial cell sarcoma has
                                                                               survival rate of 50-60 % at 5 years and
                                                                               40-50 % at 10 years. The prognosis
                                                                               depends upon histologic grade,
                                                                               anatomic location and tumor size also
                                                                               [5].


R E F E R E N C E
      1. Eilber FC, Dry SM- Diagnosis and management of synovial sarcoma. J Surg Oncol 2008,97(4):314-20. 2. Andrea Ferrari,
Paola Collini - Synovial Sarcoma. An ESUN Article in Liddy Shriver Sarcoma Initiative URL: http://sarcomahelp.org/
learning_center/synovial_sarcoma.html Accessed September 10th 2009. 3. WB Saunders, Robbins Pathologic Basis of Disease.
Seventh Edition. Elsevier Publication.2005. 4. I Fligman, F Lonardo, SC Jhanwar, WL Gerald, J Woodruff and M Ladanyi
Molecular diagnosis of synovial sarcoma and characterization of a variant SYT-SSX2 fusion transcript. American Journal of
Pathology, 147: 1592-1599. 5. Bernardo Vargas, Mark Clayer - Synovial Cell Sarcoma: Follow-up. J Clin Oncol 2000,18: 3794
,803.

2

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  • 1. International Research Journal ISSN-0975-3486 VOL. I * ISSUE—3&4 RNI : RAJBIL/2009/30097 Research Paper—Medical SYNOVIAL SARCOMA : AN UNCOMMON CAUSE OF LEG SWELLING *Dr. Vipul Gurjar **Dr. R.P. Bharaney Dec.-09—Jan.-2010 [ M.S.] [M.S.] *General Surgeon, Asst. Prof. S.B.K.S. Medical College, Pipariya **General Surgeon, Prof.& Head, S.B.K.S. Medical College, Pipariya A B S T R A C T Synovial sarcoma is known as soft tissue sarcoma and it is a rare form of cancer which usually occurs near the joints of the limbs. Here we are presenting a case of young male having leg lump which was investigated and operated for wide excision and later on he advised for post operative above knee amputation and Chemo-Radiotherapy as the histopathology of tumour showed poorly differentiated cells. KEYWORDS— soft tissue leg swelling ; malignant tumour ; synovial sarcoma. INTRODUCTION: excision of lump. Histopathology showed poorly Synovial sarcomas are malignant tumours of non- differentiated cells. Later, patient was given advice for epithelial extra skeletal tissue of the body and it above knee amputation and chemo – radiotherapy . accounts for 8% of all soft tissue sarcoma. Primary synovial sarcoma occurs most commonly in the soft tissue near larger joints of limbs but it may involve most human tissue and organs like Brain, Heart and Prostate. These tumours are rare with an annual incidence of around 2-3 /100000 they account for less than 1% of all malignant tumours and 2% of all cancer related death, although in children soft tissue sarcoma represent about 8% of all malignancy. It mainly occurs in 3 rd decades of life of young males. [1,2]. CASE REPORT: A 22 year old male patient presented with a swelling in upper leg. On examination there was a 6×6 cm, globular, firm swelling near popliteal fossa with normal peripheral pulsation. X-ray of leg showed soft tissue swelling & the bones were normal. Other routine investigations like blood count, chest x-ray, USG FIG:1: LEG LUMP abdomen were normal. Patient was operated for wide çÚUâ¿ü °ÙæçÜçââ °‡ÇU §ßñËØé°àæÙ 1
  • 2. International Research Journal ISSN-0975-3486 VOL. I * ISSUE—3 &4 RNI : RAJBIL/2009/30097 FIG:2:EXCISED MASS DISCUSSION: The pathogenesis and risk factors of synovial sarcoma are still unknown though the cells of it have a microscopic appearance similar to that of the synovium giving the disease its name [2]. Two cell types can be seen microscopically, first is fibrous type or spindle cell and the second is epithelial in appearance. The classical Synovial sarcoma has a biphasic appearance with both types present. In poorly differentiated or monophasic variety it consists only of sheets of spindle cells [3]. In more than 80 % of synovial sarcoma the translocation t(x;18) (p 11;q 11) is seen [4]. Surgical wide excision is an important treatment of FIG:3: HISTOPATHOLOGY (REF. NO-5) synovial sarcoma. A tumor free margin of 1-3 cm. is recommended. But when tumor involves neurovascular or deeper plane and the tumour is large enough more than 5cm in size then amputation is the surgery of choice [1, 2, 5]. Adjuvant chemotherapy and neoadjuvant chemotherapy have been proposed for patient with metastatic soft tissue sarcoma [5]. Radiotherapy plays a well defined role in local control of disease as well as when tumour size is large [5]. Synovial cell sarcoma has survival rate of 50-60 % at 5 years and 40-50 % at 10 years. The prognosis depends upon histologic grade, anatomic location and tumor size also [5]. R E F E R E N C E 1. Eilber FC, Dry SM- Diagnosis and management of synovial sarcoma. J Surg Oncol 2008,97(4):314-20. 2. Andrea Ferrari, Paola Collini - Synovial Sarcoma. An ESUN Article in Liddy Shriver Sarcoma Initiative URL: http://sarcomahelp.org/ learning_center/synovial_sarcoma.html Accessed September 10th 2009. 3. WB Saunders, Robbins Pathologic Basis of Disease. Seventh Edition. Elsevier Publication.2005. 4. I Fligman, F Lonardo, SC Jhanwar, WL Gerald, J Woodruff and M Ladanyi Molecular diagnosis of synovial sarcoma and characterization of a variant SYT-SSX2 fusion transcript. American Journal of Pathology, 147: 1592-1599. 5. Bernardo Vargas, Mark Clayer - Synovial Cell Sarcoma: Follow-up. J Clin Oncol 2000,18: 3794 ,803. 2