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PRESENTED BY: DR. NADEEM SARDAR
1st Year PGT, Dept of Orthpaedics,SMCH
 Acquired development of non neoplastic heterotopic ossification
within soft tissues
 Most often in response to localized trauma
 Although the process most commonly develops within skeletal
muscle, the term itself is a misnomer, because nonmuscular tissue
may be involved, and inflammation is rare.
 Adolescents & young adults, predominantly men, are affected
most frequently, although it has been reported in infancy as well
 PRECIPITATING FACTORS –
 Single or repetitive trauma (70%)
 Severe thermal injury
 Post-traumatic paraplegia
 Brain injury
 Orthopaedic operations – THR
GENETIC & DEVELOPMENTAL FORMS –
 Fibrodysplasia ossificans progressiva
 Progressive osseous heteroplasia
 Pseudomalignant heterotopic ossification
 Albright hereditary osteodystrophy
 Parosteal fasciitis
 1. NON HEREDITARY MYOSITIS OSSIFICANS
 2.MYOSITIS OSSIFICANS PROGRESSIVA
(“FIBRODYSPLASIA OSSIFICANS PROGRESSIVE”)
 Occur in children(due to periosteum is loosely attached around bones)
and in young active males due to trauma to the muscle and soft
tissues(hematoma in muscles)
 Massage following fracture can aggrevate this condition
 Muscles usually involved are -
 Quadriceps
 Brachialis
 Gluteal muscles
 Deltoid
 Also called Fibrodysplasia ossificans progressiva OR STONE
MAN SYNDROME
 Autosomal dominant connective tissue disorder
 Muscle tissue and connective tissue –tendons & lig.gradually
replaced by bone (ossified), extra-skeletal or heterotopic bone
that constrains movement
 No cure
 Usualy die early - malnutrition & recurrent infections
 Painful lumps and stiffness in the adjoining joint.
 Lumps decrease in a few weeks, but joint mobility reduction persists
EXACERBATING FACTORS FOR OSSIFICATIONS AT NEW
SITES ARE-
 Minor trauma
 Venipuncture
 Biopsy of lumps
 IM injections,
 Dental treatments
 Ossification progresses from proximal to distal and cranial to caudal.
CLINICAL FEATURES-
Digits:
 Short hallux in valgus with synostosis short thumbs
 Clinodactyly
 Fibrous Tissues:
 Swelling in aponeurosis, fasciae, and tendons
 Ossification in muscles and fibrous tissue
 Most prominent in the neck, dorsal trunk and proximal extremities
 The sternocleidomastoid muscle is commonly affected
 Kyphoscoliosis
Myositiss Ossificans Progressiva- (left) Dorsal view of
patient (upper) B/L clindodactyly of 5th finger of
hands (below) B/L short hallux valgus of feet
Xray showing B/L short hallux valgus
HISTOPATHOLOGY-
 Four distinct zones:
 1. Central undifferentiated zone- Mitotically active
 2. Surrounding zone of immature osteoidformation – Less active
 3. Zone with new bone – Osteoblast & fibroustissue with trabecular
organization
 4. Peripheral zone of fibrous tissue
 At least 10 days are required following onset of symptoms for these zones
to become apparent.
Myositis Ossificans- Histopathology
CLINICAL FEATURES-
 Typically begin approximately 1 to 3 weeks after an injury
 Localized pain and a palpable mass.
 Increased warmth, swelling
 Progressive loss of ROM - Hallmark sign
 Low-grade fever
 Mildly elevated ESR
RADIOGRAPHIC FEATURES-
 Early plain radiograph-
 Non calcified mass in the soft tissues
 Within 2 to 4 weeks after the injury –
 Floccular calcifications begin to appear within the mass
 If the cambium layer of the periosteum was involved in the
initial injury, a periosteal reaction of the underlying bone
 Over a 6 to 8 wk period - serial x-rays at 1 to 2 wk intervals
show-
 Peripheral osseous maturation of the lesion
 Central lucent zone and a lucent line separating it from the
underlying cortex , distinguishing from an extraosseous
sarcoma
 After5 to 6 months - mature bone is evident, and the lesion
may show a decrease in overall size
MYOSITIS OSSIFICANS- A. Knee B. Elbow
FIBRODYSPLASIA OSSIFICANS PROGRESSIVA
 CT scan –
 Delineats the zonal maturation and cortical separation when the
diagnosis is unclear
 Other imaging modalities –
 Bone scintigraphy
 Ultrasound
 MRI
 Leukocyte scanning, and angiography, particularly in early lesions or in
difficult cases
CT scan shows Egg shell calcification
 Parosteal Osteosarcoma
 Soft tissue Sarcoma including malignant fibrous
histiocytoma
 Synovial sarcoma
 As the calcifications will typically resolve after a period of time,
non-surgical treatment is encouraged.
 Affected limb should be immobilized with bed rest, ice therapy,
and elevation of the affected limb.
 Range of motion exercise can be introduced as long as the range
of motion is not painful.
 For those who had total hip replacement postoperative single
low-dose radiation with 3 weeks of oral indomethacin regimen
will be preventive.
INDICATION OF SURGICAL EXCISION –
 Intolerable pain
 Compression of the neurovascular structures
 Limitation of the range of motion of the joint which
affects the activities of daily living.
Thanks

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Myositis ossificans

  • 1. PRESENTED BY: DR. NADEEM SARDAR 1st Year PGT, Dept of Orthpaedics,SMCH
  • 2.  Acquired development of non neoplastic heterotopic ossification within soft tissues  Most often in response to localized trauma  Although the process most commonly develops within skeletal muscle, the term itself is a misnomer, because nonmuscular tissue may be involved, and inflammation is rare.  Adolescents & young adults, predominantly men, are affected most frequently, although it has been reported in infancy as well
  • 3.  PRECIPITATING FACTORS –  Single or repetitive trauma (70%)  Severe thermal injury  Post-traumatic paraplegia  Brain injury  Orthopaedic operations – THR
  • 4. GENETIC & DEVELOPMENTAL FORMS –  Fibrodysplasia ossificans progressiva  Progressive osseous heteroplasia  Pseudomalignant heterotopic ossification  Albright hereditary osteodystrophy  Parosteal fasciitis
  • 5.  1. NON HEREDITARY MYOSITIS OSSIFICANS  2.MYOSITIS OSSIFICANS PROGRESSIVA (“FIBRODYSPLASIA OSSIFICANS PROGRESSIVE”)
  • 6.  Occur in children(due to periosteum is loosely attached around bones) and in young active males due to trauma to the muscle and soft tissues(hematoma in muscles)  Massage following fracture can aggrevate this condition  Muscles usually involved are -  Quadriceps  Brachialis  Gluteal muscles  Deltoid
  • 7.  Also called Fibrodysplasia ossificans progressiva OR STONE MAN SYNDROME  Autosomal dominant connective tissue disorder  Muscle tissue and connective tissue –tendons & lig.gradually replaced by bone (ossified), extra-skeletal or heterotopic bone that constrains movement  No cure  Usualy die early - malnutrition & recurrent infections
  • 8.  Painful lumps and stiffness in the adjoining joint.  Lumps decrease in a few weeks, but joint mobility reduction persists EXACERBATING FACTORS FOR OSSIFICATIONS AT NEW SITES ARE-  Minor trauma  Venipuncture  Biopsy of lumps  IM injections,  Dental treatments  Ossification progresses from proximal to distal and cranial to caudal.
  • 9. CLINICAL FEATURES- Digits:  Short hallux in valgus with synostosis short thumbs  Clinodactyly  Fibrous Tissues:  Swelling in aponeurosis, fasciae, and tendons  Ossification in muscles and fibrous tissue  Most prominent in the neck, dorsal trunk and proximal extremities  The sternocleidomastoid muscle is commonly affected  Kyphoscoliosis
  • 10. Myositiss Ossificans Progressiva- (left) Dorsal view of patient (upper) B/L clindodactyly of 5th finger of hands (below) B/L short hallux valgus of feet
  • 11. Xray showing B/L short hallux valgus
  • 12.
  • 13. HISTOPATHOLOGY-  Four distinct zones:  1. Central undifferentiated zone- Mitotically active  2. Surrounding zone of immature osteoidformation – Less active  3. Zone with new bone – Osteoblast & fibroustissue with trabecular organization  4. Peripheral zone of fibrous tissue  At least 10 days are required following onset of symptoms for these zones to become apparent.
  • 14.
  • 16. CLINICAL FEATURES-  Typically begin approximately 1 to 3 weeks after an injury  Localized pain and a palpable mass.  Increased warmth, swelling  Progressive loss of ROM - Hallmark sign  Low-grade fever  Mildly elevated ESR
  • 17. RADIOGRAPHIC FEATURES-  Early plain radiograph-  Non calcified mass in the soft tissues  Within 2 to 4 weeks after the injury –  Floccular calcifications begin to appear within the mass  If the cambium layer of the periosteum was involved in the initial injury, a periosteal reaction of the underlying bone  Over a 6 to 8 wk period - serial x-rays at 1 to 2 wk intervals show-  Peripheral osseous maturation of the lesion  Central lucent zone and a lucent line separating it from the underlying cortex , distinguishing from an extraosseous sarcoma  After5 to 6 months - mature bone is evident, and the lesion may show a decrease in overall size
  • 18. MYOSITIS OSSIFICANS- A. Knee B. Elbow
  • 19.
  • 21.  CT scan –  Delineats the zonal maturation and cortical separation when the diagnosis is unclear  Other imaging modalities –  Bone scintigraphy  Ultrasound  MRI  Leukocyte scanning, and angiography, particularly in early lesions or in difficult cases
  • 22. CT scan shows Egg shell calcification
  • 23.  Parosteal Osteosarcoma  Soft tissue Sarcoma including malignant fibrous histiocytoma  Synovial sarcoma
  • 24.  As the calcifications will typically resolve after a period of time, non-surgical treatment is encouraged.  Affected limb should be immobilized with bed rest, ice therapy, and elevation of the affected limb.  Range of motion exercise can be introduced as long as the range of motion is not painful.  For those who had total hip replacement postoperative single low-dose radiation with 3 weeks of oral indomethacin regimen will be preventive.
  • 25. INDICATION OF SURGICAL EXCISION –  Intolerable pain  Compression of the neurovascular structures  Limitation of the range of motion of the joint which affects the activities of daily living.