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SOFT%20TISSUE%20TUMORS%20%20Early%20diagnosis

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ANY MUSCULAR LESION WHICH DOES NOT EVOLVE BETWEEN 2 CONTROLS HAS TO MAKE EVOKE A ... Limousin. Midi-Pyr n es. Pays de Loire. IPSSar. CONSTATS ... – PowerPoint PPT presentation

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Title: SOFT%20TISSUE%20TUMORS%20%20Early%20diagnosis


1
SOFT TISSUE TUMORS Early diagnosis
Nicolas SANS Hôpital Universitaire Purpan -
Toulouse - FRANCE
2
This is not a muscular tear
RHADOMYOSARCOMA
3
This is not a popliteal cyst
LYMPHOMA
4
This is not an intramuscular hematoma
5
ANGIOSARCOMA
ANY MUSCULAR LESION WHICH DOES NOT EVOLVE BETWEEN
2 CONTROLS HAS TO MAKE EVOKE A TUMOR
6
EPIDEMIOLOGY
  • BENIGN TUMORS 300 /100 000
  • MALIGNANT TUMORS 3 /100 000

Kransdorf et Murphey, 1997
Soft Tissue Sarcomas 2000 new cases per year in
France
7
CAT
  • The rarity and the anatomo-clinical
    heterogeneousness returns the difficult treatment
  • The vital and functional future is strongly
    dependent on the initial treatment of the tumor
  • A multidisciplinary approach is necessary and,
    it, from the diagnostic time to the post
    therapeutic time

8
NATURAL HISTORY
Centrifugal Longitudinal Fibro-vascular
reaction
9
NATURAL HISTORY
Centrifugal Longitudinal Fibro-vascular
reaction Capsule (B) Pseudo capsule (M)
10
PHYSICAL SIGNS
  • deep mass, often little painful
  • duration of the symptoms ?
  • recent increase of volume ?
  • diameter gt 5 cm

11
PROGNOSTIC FACTORS
  • Age gt 50 ans
  • Male ()
  • Location head, neck, chest
  • Histological grade
  • Histological type ()
  • SURGICAL MARGINS

12
The PROGNOSTIC depends on the initial surgical
treatment
  • R0
  • all tumour tissue was macroscopically removed
    with microscopically clear margins
  • recurrence 10 for 5 years
  • R1
  • microscopic residual disease or with close
    margins (less than 1 mm)
  • recurrence 50 for 5 years
  • R2
  • macroscopic residual disease
  • recurrence 90 for 5 years

Post operative irradiation cant improve an
incorrect surgery
13
COMPARTMENTAL ANATOMY
Muscular fascia Enthesis Cartilage Cortical
bone Periost
UNI PLURI
Anderson MW et al. AJR 1999
14
MEDICAL IMAGING
15
GOALS
  1. To define the most sensitive technique in the
    detection of the masses of soft tissues
  2. To estimate the most specific technique as for
    the differentiation between a benign and
    malignant tumor
  3. To appreciate the operability and participate in
    the therapeutic planification
  4. To approach the histological nature

16
INITIAL DIAGNOSIS
In few cases images are pathognomonic
17
Elastofibroma
18
Fibrolipoma of the median nerve
Courtesy D Godefroy
19
PLAIN RADIOGRAPHS
  • Frequently unrewarding

20
PLAIN RADIOGRAPHS
  • Sometimes evokes the diagnosis

21
SONOGRAPHY
  • cystic vs solid lesions
  • calficiations
  • to eliminate an hematoma

22
CT
Lipoma
Ossificans myositis
23
MRI
  • Morphological Analysis - Signal analysis
  1. Multiplanar study (axial )
  2. T1 weighted - T2 weighted
  3. Pre and post Gadolinium injection
  4. With and without fat saturation
  5. Dynamic study
  6. MRA

24
Depth Size
Superficial  benign  If size lt 3 cm
Deep  malignant  If size gt 5 cm
25
well defined margins
Sarcoma
26
  • Poor defined margins

T
Hematoma
27
Poor defined margins
Desmoid tumor
28
Vascular and/or nervous contact
29
Surgical planification
30
Crossing a Fascia
Extra compartmental
31
Crossing a Fascia
Fibromatosis Vascular tumor Nervous tumor
32
NOT WITHOUT FAT SAT !!!
Synovialosarcoma
Gielen, JCAT 2003
33
NOT WITHOUT FAT !!!
T1 Fat Sat Gado
34
NOT WITHOUT FAT !!!
T1 Fat Sat Gado
35
  • IN FAVOR OF MALIGNANCY
  • Heterogeneous T1
  • T1 homogeneous ? T2 heterogeneous
  • Low signal intensity of the septa on T2
  • Necrosis represents more than 50 of the lesion

Hermann et al. BJR 1992 6514-20
36
SIGNAL ANALYSIS
37
Heterogeneous or hyperintense on T1
Synovialosarcoma
Liposarcoma
Se Sp ---
38
Homogeneous signal on T1
Heterogeneous on T2
T1
T2
Se 72-80 Sp 87-91
Leiomyosarcoma
39
Low signal intensity of the septa on T2
Liposarcoma
40
Fast and prolonged enhancement
T2
T1 Fat Sat Gado
41
Necrosis gt 50
42
MRI
  1. Lesion of more than 50 mm in diameter
  2. Deep localization
  3. Irregular or lobulated margins
  4. Irregular or tick septa
  5. Heterogeneous signal on T1 and T2
  6. Low signal intensity of the septa on T2
  7. Fast and prolonged enhancement
  8. Necrosis more than gt 50

MORPHOLOGY
SIGNAL
KRANSDORF, 2000 DESCHEPPER, 2000 VARMA,
1999CEUGNART,2002
43
PATHOLOGY
44
PATHOLOGY
GOALS
  1. To differentiate begnin or malignant tumor
  2. To confirm that it is indeed a conjunctival tumor
    (vs lymphoma, metastasis)
  3. Define the type of surgery which must be realized
    (enucleation for conjunctival tumor, extended
    resection for sarcoma)
  4. To discuss a neoadjuvant treatment

45
PATHOLOGY
  1. Microbiopsy
  2. Biopsy excision
  3. Surgical biopsy

46
PATHOLOGY
  • Tissue sample
  • Formol fixation
  • Freezing - Cryosection
  • molecular study

X
47
PATHOLOGY
  • Tissue sample
  • Formol fixation
  • Freezing - Cryosection
  • molecular study

X
Pathologist !
48
PATHOLOGY
  • Tissue sample
  • Formol fixation
  • Freezing - Cryosection
  • molecular study

X
Pathologist !
49
BIOPSY
What you should not make
  1. Perform the biopsy before the MRI
  2. Compromise or complicate the later treatment by
    an unsuitable way

50
BIOPSY
What you should not make
  1. Perform the biopsy before the MRI
  2. Compromise or complicate the later treatment by
    an unsuitable way
  3. Obtain insufficient samples

51
STAGING
52
CONCLUSION (1)
  • The initial medical management of a soft tissue
    sarcoma is essential for the future of patient
  • Think of a sarcoma when
  • Size more than 5 cm
  • Deep
  • Symptomatic lesion

53
CONCLUSION (2)
MULTIDISCIPLINARY CONCERTATION
  • MRI
  • Discuss the therapeutic plan before any surgical
    procedure
  • Biopsy
  • Experimented pathologist
  • Freezing
  • PHRC

54
Impact dun Programme dintervention de Santé
publique ciblé sur la prise en charge initiale
des SARcomes des tissus de ladulte
  • Aquitaine
  • Languedoc-Roussillon
  • Limousin
  • Midi-Pyrénées
  • Pays de Loire

IPSSar
55
CONSTATS
  • Non conformité de la prise en charge initiale
    malgré la diffusion de recommandations nationales
  • Méconnaissance clinique et radiologique
  • Multiplicité des intervenants sites
    spécialisés ?

PAYS SCANDINAVES (1989) prise en charge
spécialisée dans 80 des cas
56
OBJECTIFS
  • Mise en place dactions collectives pour
    améliorer la prise en charge des STM de ladulte
    (diagnostic bilan initial)
  • Mesurer limpact en terme de
  • proportion de prise en charge globale adéquate
  • survie
  • Estimer lincidence régionale des sarcomes en
    collaboration avec les registres départementaux
    des cancers des régions étudiées
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