MedPix® Patient Chart - Case No: 11955 :: Imaging - Review Images

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History

Age: 37 :: Gender: woman

Patient History

37 y.o. woman with chronic leg pain.

Exam


Physical Exam and Laboratory


Findings


Summary of Findings

• Multiple sessile and pedunculated osseous lesions
• These have continuity with both the cortex and the medullary cavity


Diffferential


Differential Diagnosis

• Osteochondromas (exostoses)
• Chondrosarcoma >> osteosarcoma


Diagnosis


Case Diagnosis

Dx: Hereditary Multiple Exostoses


Dx Confirmed by: Pathology for one resected lesion

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Followup


Followup and Treatment

Surgical resection of symptomatic lesions. Continued imaging follow up.

Topic


Hereditary Multiple Exostoses

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Hereditary multiple exostoses (HME) is an autosomal dominant condition resulting in multiple osteochondromas. In western populations the prevalence is approximately 1:50,000-100,000. Common clinical presentations include pain and cosmetic deformity.

Osteochondromas may be sessile or pedunculated and are the result of a separated cartilaginous fragment of the epiphyseal growth plate, which has herniated through the normal periosteal bone cuff (notch of Ranvier). This fragment continues to grow, resulting in an osseous protuberance with direct medullary continuity and a cartilaginous cap. Consequently, these lesions are typically found in a juxta-epiphyseal distribution.

Complications of osteochondromas include fracture, mass effect (vascular compromise and neurologic sequelae), bursa formation/inflammation (secondary to abnormal frictional forces), and malignant transformation. Malignant transformation occurs in approximately 1% of solitary osteochondromas and has been reported in approximately 3-5% of HME patients. The most commonly associated malignancy is chondrosarcoma but osteosarcoma is another possibility, albeit less likely.

There are several concerning radiographic findings which may suggest malignant transformation:
• Continued growth in a skeletally mature patient
• Irregular/indistinct surface
• Focal radiolucency
• Erosion/destruction of adjacent bone
• Soft tissue mass (with scattered irregular calcifications)

Finally, and perhaps the most important criterion, is a cartilaginous cap thickness greater than 1.5cm. This can be measured with ultrasound, CT and MRI.

REFs


References and Supporting Materials

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:: PT: 11955 :: :: 4 questions

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History:
37 y.o. woman with chronic leg pain.

Exam:


Findings:
• Multiple sessile and pedunculated osseous lesions
• These have continuity with both the cortex and the medullary cavity

Differential:
• Osteochondromas (exostoses)
• Chondrosarcoma >> osteosarcoma

Diagnosis:
Hereditary Multiple Exostoses
Confirmed by:Pathology for one resected lesion

Treatment and Followup:
Surgical resection of symptomatic lesions. Continued imaging follow up.

Discussion:

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Case Contributor and Editor
Topic Author: P. Gabriel Peterson
Submitted by: P. Gabriel Peterson - Author Info
Case/Image Editor: James G. Smirniotopoulos, M.D. - Editor Info
Case Accepted: 2008-04-28 09:28:34-04 :: Revised: :: Submitted:
COW: 408 :: CME Start: 20080428 :: CME End: 20110417 :: CME Review Due: 20110428

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