The synovial cell sarcoma is a malignant soft tissue tumour which most
ly occurs associated with or in a large joint. To date, the histogenet
ic origin has been discussed controversially and there is still no agr
eement as to whether it arises from normal synovium of joints, tendon
sheaths or bursae, specialised forms of mesenchymal tissue (arthrogeno
us mesenchyma) or ordinary connective tissue. The tumour rarely occurs
in the head and neck region. Only about 76 cases world-wide have been
described up to now We report on a case of a 30-year old man with a s
ynovial cell sarcoma of the temporomandibular joint and a case of a 70
-year old man with a synovial cell sarcoma of the hypopharynx. In the
first case, although all possible therapeutical efforts were made (rad
ical operation, radiotherapy, chemotherapy), recurrence of the tumour
occurred locally, as well as metastases in the lungs and bones. The pa
tient died three and a half years after the initial diagnosis of the t
umour. The second patient suffered multiple metastases in the lungs an
d bones one year after operation followed by chemotherapy. To the pres
ent time there is no general agreement on how to treat synovial cell s
arcomas, but without doubt first of all radical surgical excision must
be performed if possible. Additional radiation and/or multidrug chemo
therapy may be useful in special cases. In our opinion every case of s
ynovial cell sarcoma should be published because it is of importance t
o get to know new aspects and therapeutical possibilities of this rare
disease.