Weekly Case

Title : case 204

Age / Sex : 30 / M




Age/Sex : 30/M



 



Chief complaint : left ankle
swelling






1) What is your impression?



Two weeks later, you can see the final diagnosis with a brief discussion of
this case.



* Send Application Answers to In Sook Lee, MD (lis@pusan.ac.kr)



Courtesy : Young-sook
Kim, M.D., / Chosun
university hospital






Diagnosis:

pigmented villonodular synovitis (PVNS)



Discussion




Findings :



Simple : left ankle lateral view shows soft tissue mass in
posterior ankle joint area without obliteration of Kager’s fat triangle



MRI : ill defined, lobulated,
bulcky mass with iso or slight high SI to muscle on T1WI, mixed SI on T2WI and
heterogeneous enhancement on post-contrast image in supracalcaneal fat triangle
area. mass infiltrated posterior TF joint and posterior aspect of FHL tendon



 



Differential
Diagnosis :



Synovial sarcoma



Synovial chondromatosis



Hemophilia



Rheumatoid arthritis



Lipoma arborescence



 



Discussion
:



General features



-General path comments:
Locally destructive fibrohistiocytic proliferation and villonodular protrusions
of synovial membranes, affecting joints, bursae, tendon sheaths



-Genetics: Clonal chromosomal
aberrations, aneuploidy



 *Trisomies 5 and 7



-Etiology



  *Controversial:
Reactive inflammatory process



  *Low-grade,
locally aggressive neoplasm



-Epidemiology



  *5% of
all primary soft tissue tumors



  *GCTTS:
Second most common soft tissue mass of hand



 



Presentation



-Most common signs/symptoms:
Limited joint mobility



-Clinical profile



*GCTTS



    #Slowly enlarging, mobile, soft tissue mass



    #Pain increased with activity



  *PVNS



    #Joint swelling, pain of insidious onset



    #Increased skin temperature



    #Pain increased with motion, improved by
rest



    #Sudden increase in pain due to torsion of
synovial nodules



    #Decreased range of motion, joint locking



    #Joint effusion:
Serosanguinous/xanthochromic fluid



    #Recurrent sanguinous effusions without
history of trauma



    #Rapid accumulation of joint fluid after
aspiration



    #Pathologic fracture secondary to
subchondral bone invasion can be seen



 



Demographics



-Age



  *GCTTS: 30-50 years, mean: 32years



  *PVNS: 30-40 years, childhood appearance
reported



-Gender



  *GCTTS: M:F=1:1



  *PVNS: F:M=2:1



 



Natural
history & prognosis



-Benign,
locally aggressive lesion



-Progressive
destruction of articular cartilage and subchondral bone results in severe
osteoarthritis



-PVNS:
Recurrence 20-50%



 



References :



De Beuckeleer L et al:
Magnetic resonance imaging of localized giant cell tumor of the tendon
sheath(MRI of localized GCTTS). Eur Radiol 7:198-201, 1997



Cotton A et al: Pigmented
villonodular synovitis of the hip: Review of radiographic features in 58
patients. Skeletal Radiol 24:1-6, 1995



Hughes TH et al: Pigmented
villonodular synovitis: MRI characteristics. Skeletal Radiol 24:7-12, 1995



Abdul-Karim EW et al: Diffuse
and localized tenosynovial giant cell tumor and pigmented villonodular
synovitis: A clinicopathologic and flow cytometric DNA analysis. Hum Pathol
23:729-35, 1992





Correct Answer
Name Institution
total applicants 18
correct answer 7
이승훈 한양대학교병원
윤민아 서울대학교병원
이경규 한강성심병원
조신영 웰튼병원
김인환 전북대학교병원
이신우 가천의대길병원
정진영 삼성의료원
semi-correct answer 2
김성현 자생의원
공근영 자생의원

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