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MULTIPLE WELL DEFINED RADIOLUCENCIES
www.indiandentalacademy.com
INDIAN DENTAL ACADEMY
Leader in continuing Dental Education
Anatomic variants:
Focal osteoporotic bone marrow defects
Separate marrow spaces
Multiple post extraction sockets
www.indiandentalacademy.com
 Pathology :
Multiple cysts or
granulomas
Basal cell nevus
syndrome
Multiple myeloma
Metastatic carcinoma
Langerhan’s cell disease
 Rarities
Ameloblastoma
Cherubism
Craniofacial dysostosis
Florid cementosseous dysplasia
Giant cell granuloma
Hyperparathyroidism
Lymphomas
Neurofibromatosis
Noonan’s syndrome
Oxalosis
Papillon-lefevre syndrome
Scleroderma
Traumatic bone cyst
Systemic sclerosis
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Focal osteoporotic bone marrow
defects
 May produce the radiographic image of a
cyst like rl
 They are comon in mandible post region
 Female
 r/f varies from cyst like to multilocular to
irregular and borders are well defined
 Rarely shows cortical expansion
 They are seen at the apices of the teeth
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Focal osteoporotic
defects
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Focal osteoportoic defect
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Multiple extracted sockets
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Marrow spaces
The trabecular pattern in the
posterior mandible is quite variable,
generally showing large marrow
spaces and sparse trabeculation,
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Multiple Cysts Or Granulomas
 Dentigerous cyst
 Radicular cyst
 Primordial cyst
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Basal cell nevus syndrome
 It is a autosomal dominant trait with variable
expressivity
 M=F
 Age: 5 & 30 yrs
 Cutaneous & skeletal abnormalities( multiple cysts of
jaw,bifid ribs,vertebral fusion,polydacty,mild
prognastism)
 Ectopic calcification
 Nevoid basal cell carcinoma
 Dyskeratosis on palmar and plantar surfaces
 Jaw cysts –dentigerous cysts,primodial or radicular
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MultipleOKCsassociatedwithnevoidbasalcellcarcinomasyndrome.
A,Upperarrowspointtoopacifiedmaxillaryantra;smallerarrowindicatesthe
extensionofoneofthemandibularcysts(lowerarrows)intothebifurcationregion
ofamandibularmolar.
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Basal cell nevus syndrome showing multiple
cysts in different parts of mandible
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Multiple myeloma
Synonym: Myeloma,Plasma cell myeloma, Plasmacytoma
 It is defined as a chronic, progressive neoplastic
proliferation of the plasma cells which produces
immunoglobulins, occurring principally in the bone
marrow, but which may also appear in other organ
systems
Most common malignancy of bone in adults
 Single lesions –Plasmacytoma
 Multipe lesions-Multiple Myeloma
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Clinical features
 4th to 7th
 Male predileciton
 Bone pain , Anemia, low back pain (typical
feature)
 Secondary signs : Amyloidosis, Hypercalcemia
 Bence jones proteins-50% patients
 when clonal proliferation occurs it replaces
cancellous bone later cortical border replacing the
normal RO bone with areas of RL
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ORAL FINIDINGS
 Pain, paresthesia;,mucosal ulcerations,swelling, soft
tissue mass, tooth mobility,tooth migration,
Amyloid deposition in the tongue and other oral
tissues, and pathological fracture.
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Radiographic findings
 Type 1: Solitary type (similar to bone cyst)
 Type 2: Multiple osteolytic lesions without
marginal sclerosis (a. central type, and b.
peripheral type)
 Type 3: Diffuse osteoporosis with generalized
involvement
 Type 4: Diffuse osteosclerosis.
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Diffuse Osteosclerosis
a) Diffuse
b) Focal osteocondensation
c) Bony speculation on the surface of the bone
d) Sclerotic reaction at the rim of lytic lesion.
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Radiographic Manifestations
The multiple lesions may be few or many
They are commonly rounded , with eighter well-
defined or fairly well-defined margins but lacks
cortication (punched out) ,some lesions may be
irregular (secondary cancer)
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 Adjacent lesions often meet as they enlarge so that a
remnant of bone left between lesions-
 The result of the formation of adjacent lesions is that
the surface of the bone is deformed –rippled
appereance
 Separate areas of bone destruction varying in size
from few mm to many inches
 In advanced cases there are thousands of such
rounded rl scattered - riddled appereance
 Maxilla and mandible are rarely affected
Many very small lesions not over 3mm are seen but
seldom reaches 1cm
Margins are usually fairly sharp
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CRITERIA
 Clonal plasma cells are present on biopsy of
bonemarrow or plasmacytoma
 M-protein is present in serum or urine (either
intact immunoglobulin or free light chains)
 Evidence of related organ or tissue impairment is
present (lytic bone lesions; renal insufficiency;
anemia; hypercalcemia; hyperviscosity;
amyloidosis; or recurrent infections).
www.indiandentalacademy.com
D/D
 Metastatic tumors
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Lateral skull view showing
multiple
punched out radiolucent
lesions scattered throughout
the
entire skull
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Multiple Myeloma With Osteoporosis
 It is a very rare entity which involves the
greater part of skeleton and jaws
 Whole of the bone appears unusually dark
and the trabeculae may be diffcicult to
identify –except for the persistacne of cortical
margins
d/d:
Hyperparathyroidism
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Solitary myeloma
Jaws are uncommon sites to occur
2 main types:
1st type-An area of bone destruction is well demarcated
from surrounding bone ,some times may be corticated
Sub periosteal new bone may form
Trabeculae –thin or coarse
2nd type-purely destructive with no new bone at the
margins surrounding the tumor ,
The margins shows infilteration
Flat bones- sausage shaped lesions with undulating
margins
www.indiandentalacademy.com
Cropped
panoramic
image shows
a solitary
lesion in the
condylar
neck region
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Effects on surrounding structure
 Teeth may appear as too RO
 Lamina dura and follicles of impacted tooth
may lose their typical corticated surrounding
bone
 Thinning of lower border of mandible ,or
endosteal scalloping
 Periosteal reaction is rare but if present takes
the form of single RO line or more rarely
sunray appereance
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Langerhan Cell Histocytosis
Synonym: Idiopathic histiocytosis,histiocytosis X
 Acute disseminated form –letterer-siwe
disease
 Chronic disseminated form-hand-schuller-
christian
 Chronic localized form-eosinophilic
granuloma
www.indiandentalacademy.com
Acute disseminated Chronic disseminated Chronic localized
disseminated
Age Infants under 1yr of age Children & young
adults
Adults & juvenile
Clinical
manifestati
ons
Enlargement of organs
and other swellings
Cachectic,petechiae &
necrotic ulcer ,severe
pancytopenia
3- bony lesions,
exophthalamus & DI
Male predominance
Oral
manifestati
ons
Necrotic ulcers
Petechiae
Mobility of teeth &
gingival bleeding
Ulcerations
Edematous gingiva
Loosened teeth
Destruction of dental follicle
Missing teeth
R/F Multiple small rounded
RL with well defined
borders
BL appear ragged n
may coalasce –
geographi c
appeareance
Proliferative periostitis,with
radiolucet ragged borders-
juvenile
Sclerosig borders in adults
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Alveolar process Intraosseous
 Multiple
 Mandibular posterior
region
 Well defined without
cotiction
 Lesion starts from mid root
region of tooth
 Scooped out shape
 Solitary
 Mandibular ramus
 Well defined
 Shape is irregular or oval
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Surrounding Structure
 Teeth appear to be standing in space
 The lesion does not displace teeth
 Periosteal new bone formation
 Can destroy outer ortical plate
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Differential Diagnosis
 Periodontal disease
 Squamous cell carcinoma
 Simple bone cyst
 Metastatic malignant neoplasm
 Malignant tumors from adjacent soft tissues
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Langerhans cell histiyocytosis
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A panoramic film of multiple lesions of
Langerhans' cell histiocytosis. Note the scooped-out shape
of the bone destruction in the mandible. The floor of the
right maxillary antrum has been destroyed.
www.indiandentalacademy.com
Skull lesions of Langerhans' cell histiocytosis, showing
well-defined, punchEd-out lesions.
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Metastatic Carcinoma
Establishment of new foci of malignant disease
from distinct malignant tumour usually by the
way of blood vessels.
 1-3%of all metastasis.
 Women-from breast, adrenal gland, genital
organ, thyroid gland.
 Man-lung, prostate, kidney, adrenal gland
www.indiandentalacademy.com
 Mand post region
 50-70 yrs of life
 Female predilection
 Oral neoplasm may be 1st sign of
malignancy-30%of cases.
 Enlarging tumours erode rapidly through
cortical plates.
www.indiandentalacademy.com
Radiographic Features
1.A solitary well defined cyst like r/l
2.A solitary poorly defined r/l-localized,
3.multiple, separate, poorly defined r/l-
4.multiple,punched out r/l
5.r/o patterns with any of foregoing r/l
6.Irregular salt and pepper appearance-
7.A relatively dense, solitary, r/o area
www.indiandentalacademy.com
 Secondary deposits from carcinoma may be
purely destructive(osteolytic) or they may be
bone forming (osteoblastic)
Osteolytic -2 types
 Frank destruction
 Infilteration
 Combination of area having bone destruction
and islands of bone
 Abnormality is centrally located
www.indiandentalacademy.com
 2nd lytic type
Resemblance with osteomyeltis
Infilterated margins of areas of bone
destruction
Normal bone representng islands of various
sizes seperates the areas of bone destruciton
which is in continuity with the remaning
bone
www.indiandentalacademy.com
AFFECT Of SURROUNDING STRUCTURES
 Periosteal reaction –speculated pattern
 Floating of teeth in air
 Extraction sockets fail to heal
 Resorption of teeth is rare
 Occasionally the tumor breaches into
surrounding soft tissue and present as an
intraoral mass
 Cortical borders of normal anatomical
structures are destroyed
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www.indiandentalacademy.com
www.indiandentalacademy.com
D/D
 Multiple myeloma
 Odontogenic cysts secondarily infected
 Squamous cell carcinoma
www.indiandentalacademy.com
references
 Principles practice oral radiologic
interpretation H.m worth
 Oral radiology principles and interpretation
5th edition white & pharaoh
 Differential diagnosis of orol and
maxillofacial lesions 5th edition norman.k
and wood,paul w.goaz
www.indiandentalacademy.com

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Multiple well defined radiolucencies / dental courses

  • 1. MULTIPLE WELL DEFINED RADIOLUCENCIES www.indiandentalacademy.com INDIAN DENTAL ACADEMY Leader in continuing Dental Education
  • 2. Anatomic variants: Focal osteoporotic bone marrow defects Separate marrow spaces Multiple post extraction sockets www.indiandentalacademy.com
  • 3.  Pathology : Multiple cysts or granulomas Basal cell nevus syndrome Multiple myeloma Metastatic carcinoma Langerhan’s cell disease  Rarities Ameloblastoma Cherubism Craniofacial dysostosis Florid cementosseous dysplasia Giant cell granuloma Hyperparathyroidism Lymphomas Neurofibromatosis Noonan’s syndrome Oxalosis Papillon-lefevre syndrome Scleroderma Traumatic bone cyst Systemic sclerosis www.indiandentalacademy.com
  • 4. Focal osteoporotic bone marrow defects  May produce the radiographic image of a cyst like rl  They are comon in mandible post region  Female  r/f varies from cyst like to multilocular to irregular and borders are well defined  Rarely shows cortical expansion  They are seen at the apices of the teeth www.indiandentalacademy.com
  • 8. Marrow spaces The trabecular pattern in the posterior mandible is quite variable, generally showing large marrow spaces and sparse trabeculation, www.indiandentalacademy.com
  • 9. Multiple Cysts Or Granulomas  Dentigerous cyst  Radicular cyst  Primordial cyst www.indiandentalacademy.com
  • 10. Basal cell nevus syndrome  It is a autosomal dominant trait with variable expressivity  M=F  Age: 5 & 30 yrs  Cutaneous & skeletal abnormalities( multiple cysts of jaw,bifid ribs,vertebral fusion,polydacty,mild prognastism)  Ectopic calcification  Nevoid basal cell carcinoma  Dyskeratosis on palmar and plantar surfaces  Jaw cysts –dentigerous cysts,primodial or radicular www.indiandentalacademy.com
  • 12. Basal cell nevus syndrome showing multiple cysts in different parts of mandible www.indiandentalacademy.com
  • 13. Multiple myeloma Synonym: Myeloma,Plasma cell myeloma, Plasmacytoma  It is defined as a chronic, progressive neoplastic proliferation of the plasma cells which produces immunoglobulins, occurring principally in the bone marrow, but which may also appear in other organ systems Most common malignancy of bone in adults  Single lesions –Plasmacytoma  Multipe lesions-Multiple Myeloma www.indiandentalacademy.com
  • 14. Clinical features  4th to 7th  Male predileciton  Bone pain , Anemia, low back pain (typical feature)  Secondary signs : Amyloidosis, Hypercalcemia  Bence jones proteins-50% patients  when clonal proliferation occurs it replaces cancellous bone later cortical border replacing the normal RO bone with areas of RL www.indiandentalacademy.com
  • 15. ORAL FINIDINGS  Pain, paresthesia;,mucosal ulcerations,swelling, soft tissue mass, tooth mobility,tooth migration, Amyloid deposition in the tongue and other oral tissues, and pathological fracture. www.indiandentalacademy.com
  • 16. Radiographic findings  Type 1: Solitary type (similar to bone cyst)  Type 2: Multiple osteolytic lesions without marginal sclerosis (a. central type, and b. peripheral type)  Type 3: Diffuse osteoporosis with generalized involvement  Type 4: Diffuse osteosclerosis. www.indiandentalacademy.com
  • 17. Diffuse Osteosclerosis a) Diffuse b) Focal osteocondensation c) Bony speculation on the surface of the bone d) Sclerotic reaction at the rim of lytic lesion. www.indiandentalacademy.com
  • 18. Radiographic Manifestations The multiple lesions may be few or many They are commonly rounded , with eighter well- defined or fairly well-defined margins but lacks cortication (punched out) ,some lesions may be irregular (secondary cancer) www.indiandentalacademy.com
  • 19.  Adjacent lesions often meet as they enlarge so that a remnant of bone left between lesions-  The result of the formation of adjacent lesions is that the surface of the bone is deformed –rippled appereance  Separate areas of bone destruction varying in size from few mm to many inches  In advanced cases there are thousands of such rounded rl scattered - riddled appereance  Maxilla and mandible are rarely affected Many very small lesions not over 3mm are seen but seldom reaches 1cm Margins are usually fairly sharp www.indiandentalacademy.com
  • 20. CRITERIA  Clonal plasma cells are present on biopsy of bonemarrow or plasmacytoma  M-protein is present in serum or urine (either intact immunoglobulin or free light chains)  Evidence of related organ or tissue impairment is present (lytic bone lesions; renal insufficiency; anemia; hypercalcemia; hyperviscosity; amyloidosis; or recurrent infections). www.indiandentalacademy.com
  • 22. Lateral skull view showing multiple punched out radiolucent lesions scattered throughout the entire skull www.indiandentalacademy.com
  • 26. Multiple Myeloma With Osteoporosis  It is a very rare entity which involves the greater part of skeleton and jaws  Whole of the bone appears unusually dark and the trabeculae may be diffcicult to identify –except for the persistacne of cortical margins d/d: Hyperparathyroidism www.indiandentalacademy.com
  • 27. Solitary myeloma Jaws are uncommon sites to occur 2 main types: 1st type-An area of bone destruction is well demarcated from surrounding bone ,some times may be corticated Sub periosteal new bone may form Trabeculae –thin or coarse 2nd type-purely destructive with no new bone at the margins surrounding the tumor , The margins shows infilteration Flat bones- sausage shaped lesions with undulating margins www.indiandentalacademy.com
  • 28. Cropped panoramic image shows a solitary lesion in the condylar neck region www.indiandentalacademy.com
  • 29. Effects on surrounding structure  Teeth may appear as too RO  Lamina dura and follicles of impacted tooth may lose their typical corticated surrounding bone  Thinning of lower border of mandible ,or endosteal scalloping  Periosteal reaction is rare but if present takes the form of single RO line or more rarely sunray appereance www.indiandentalacademy.com
  • 30. Langerhan Cell Histocytosis Synonym: Idiopathic histiocytosis,histiocytosis X  Acute disseminated form –letterer-siwe disease  Chronic disseminated form-hand-schuller- christian  Chronic localized form-eosinophilic granuloma www.indiandentalacademy.com
  • 31. Acute disseminated Chronic disseminated Chronic localized disseminated Age Infants under 1yr of age Children & young adults Adults & juvenile Clinical manifestati ons Enlargement of organs and other swellings Cachectic,petechiae & necrotic ulcer ,severe pancytopenia 3- bony lesions, exophthalamus & DI Male predominance Oral manifestati ons Necrotic ulcers Petechiae Mobility of teeth & gingival bleeding Ulcerations Edematous gingiva Loosened teeth Destruction of dental follicle Missing teeth R/F Multiple small rounded RL with well defined borders BL appear ragged n may coalasce – geographi c appeareance Proliferative periostitis,with radiolucet ragged borders- juvenile Sclerosig borders in adults www.indiandentalacademy.com
  • 32. Alveolar process Intraosseous  Multiple  Mandibular posterior region  Well defined without cotiction  Lesion starts from mid root region of tooth  Scooped out shape  Solitary  Mandibular ramus  Well defined  Shape is irregular or oval www.indiandentalacademy.com
  • 33. Surrounding Structure  Teeth appear to be standing in space  The lesion does not displace teeth  Periosteal new bone formation  Can destroy outer ortical plate www.indiandentalacademy.com
  • 34. Differential Diagnosis  Periodontal disease  Squamous cell carcinoma  Simple bone cyst  Metastatic malignant neoplasm  Malignant tumors from adjacent soft tissues www.indiandentalacademy.com
  • 37. A panoramic film of multiple lesions of Langerhans' cell histiocytosis. Note the scooped-out shape of the bone destruction in the mandible. The floor of the right maxillary antrum has been destroyed. www.indiandentalacademy.com
  • 38. Skull lesions of Langerhans' cell histiocytosis, showing well-defined, punchEd-out lesions. www.indiandentalacademy.com
  • 40. Metastatic Carcinoma Establishment of new foci of malignant disease from distinct malignant tumour usually by the way of blood vessels.  1-3%of all metastasis.  Women-from breast, adrenal gland, genital organ, thyroid gland.  Man-lung, prostate, kidney, adrenal gland www.indiandentalacademy.com
  • 41.  Mand post region  50-70 yrs of life  Female predilection  Oral neoplasm may be 1st sign of malignancy-30%of cases.  Enlarging tumours erode rapidly through cortical plates. www.indiandentalacademy.com
  • 42. Radiographic Features 1.A solitary well defined cyst like r/l 2.A solitary poorly defined r/l-localized, 3.multiple, separate, poorly defined r/l- 4.multiple,punched out r/l 5.r/o patterns with any of foregoing r/l 6.Irregular salt and pepper appearance- 7.A relatively dense, solitary, r/o area www.indiandentalacademy.com
  • 43.  Secondary deposits from carcinoma may be purely destructive(osteolytic) or they may be bone forming (osteoblastic) Osteolytic -2 types  Frank destruction  Infilteration  Combination of area having bone destruction and islands of bone  Abnormality is centrally located www.indiandentalacademy.com
  • 44.  2nd lytic type Resemblance with osteomyeltis Infilterated margins of areas of bone destruction Normal bone representng islands of various sizes seperates the areas of bone destruciton which is in continuity with the remaning bone www.indiandentalacademy.com
  • 45. AFFECT Of SURROUNDING STRUCTURES  Periosteal reaction –speculated pattern  Floating of teeth in air  Extraction sockets fail to heal  Resorption of teeth is rare  Occasionally the tumor breaches into surrounding soft tissue and present as an intraoral mass  Cortical borders of normal anatomical structures are destroyed www.indiandentalacademy.com
  • 48. D/D  Multiple myeloma  Odontogenic cysts secondarily infected  Squamous cell carcinoma www.indiandentalacademy.com
  • 49. references  Principles practice oral radiologic interpretation H.m worth  Oral radiology principles and interpretation 5th edition white & pharaoh  Differential diagnosis of orol and maxillofacial lesions 5th edition norman.k and wood,paul w.goaz www.indiandentalacademy.com

Editor's Notes

  1. b) axial CT scan, bone window; at the level of mandibular alveolar crest, exhibiting erosion of buccal and lingual cortical plates bilaterally in both the body and the lower portion of the ascending ramus, with soft tissue swelling buccally on the left side
  2. Skull view showing the ‘‘hair on end’’ appearance at the vault and the sunburst pattern
  3. Most common similar to that of the benign ginat cell tumor of bone