Enchondroma |
Micrograph of an enchondroma. H&E stain.
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Classification and external resources |
ICD-O |
9220/0 |
DiseasesDB |
33380 |
eMedicine |
article/389224 |
MeSH |
D002812 |
X-ray showing an enchondroma in the femur.
MRI T1 showing an enchondroma in the femur.
An enchondroma is a cartilage cyst found in the bone marrow. Typically, enchondroma is discovered on a X-ray scan. Enchondromas have a characteristic appearance on Magnetic Resonance Imaging (MRI) as well. They have also been reported to cause increased uptake on PET examination.
Contents
- 1 Presentation
- 2 Cause
- 3 Associated conditions
- 4 Symptoms
- 5 Diagnosis
- 6 Treatment
- 7 See also
- 8 References
- 9 External links
Presentation
Enchondroma is a type of benign bone tumor that originates from cartilage. The exact etiology of it is not known. An enchondroma most often affects the cartilage that lines the inside of the bones. The bones most often involved with this benign tumor are the miniature long bones of the hands and feet. It may, however, also involve other bones such as the femur, humerus, or tibia. While it may affect an individual at any age, it is most common in adulthood. The occurrence between males and females is equal. It is not very likely that the enchondroma will grow back in the same spot; the rate is less than ten percent.
Cause
While the exact cause of enchondroma is not known, it is believed to occur either as an overgrowth of the cartilage that lines the ends of the bones, or as a persistent growth of original, embryonic cartilage.
Associated conditions
An enchondroma may occur as an individual tumor or several tumors. The conditions that involve multiple lesions include the following:
Ollier disease (enchondromatosis) - when multiple sites in the body develop the tumors. Ollier disease is very rare.
Maffucci's syndrome - a combination of multiple tumors and angiomas (benign tumors made up of blood vessels).
Symptoms
Individuals with an enchondroma often have no symptoms at all. The following are the most common symptoms of an enchondroma. However, each individual may experience symptoms differently. Symptoms may include:
- Pain that may occur at the site of the tumor if the tumor is very large, or if the affected bone has weakened causing a fracture of the affected bone
- Enlargement of the affected finger
- Slow bone growth in the affected area
The symptoms of enchondroma may resemble other medical conditions or problems. Always consult your physician for a diagnosis.
Diagnosis
Because an individual with an enchondroma has few symptoms, diagnosis is sometimes made during a routine physical examination, or if the presence of the tumor leads to a fracture. In addition to a complete medical history and physical examination, diagnostic procedures for enchondroma may include the following:
- x-ray - On plain film, an enchondroma may be found in any bone formed from cartilage. They are lytic lesions that usually contain calcified chondroid matrix (a "rings and arcs" pattern of calcification), except in the phalanges. They may be central, eccentric, expansile or nonexpansile.
Differentiating an enchondroma from a bone infarct on plain film may be difficult. Generally, an enchondroma commonly causes endosteal scalloping while an infarct will not. An infarct usually has a well-defined, sclerotic serpentine border, while an enchondroma will not. When differentiating an enchondroma from a chondrosarcoma, the radiographic image may be equivocal; however, periostitis is not usually seen with an uncomplicated enchondroma.
- radionuclide bone scan - a nuclear imaging method to evaluate any degenerative and/or arthritic changes in the joints; to detect bone diseases and tumors; to determine the cause of bone pain or inflammation. This test is to rule out any infection or fractures.
- magnetic resonance imaging (MRI)[1] - a diagnostic procedure that uses a combination of large magnets, radiofrequencies, and a computer to produce detailed images of organs and structures within the body. This test is done to rule out any associated abnormalities of the spinal cord and nerves.
- computed tomography scan (Also called a CT or CAT scan.) - a diagnostic imaging procedure that uses a combination of x-rays and computer technology to produce cross-sectional images (often called slices), both horizontally and vertically, of the body. A CT scan shows detailed images of any part of the body, including the bones, muscles, fat, and organs. CT scans are more detailed than general x-rays.
Treatment
Specific treatment for enchondroma is determined by a physician based on the age, overall health, and medical history of the patient. Other considerations include:
- extent of the disease
- tolerance for specific medications, procedures, or therapies
- expectations for the course of the disease
- opinion or preference of the patient
Treatment may include:
- surgery (in some cases, when bone weakening is present or fractures occur)
- bone grafting - a surgical procedure in which healthy bone is transplanted from another part of the patient's body into the affected area.
If there is no sign of bone weakening or growth of the tumor, observation only may be suggested. However, follow-up with repeat x-rays may be necessary. Some types of enchondromas can develop into malignant, or cancerous, bone tumors later. Careful follow-up with a physician may be recommended.
See also
- List of radiographic findings associated with cutaneous conditions
References
- ^ Wang XL, De Beuckeleer LH, De Schepper AM, Van Marck E (2001). "Low-grade chondrosarcoma vs enchondroma: challenges in diagnosis and management". European radiology 11 (6): 1054–1057. doi:10.1007/s003300000651. PMID 11419152.
Tumours of bone and cartilage (ICD-O 9180–9269) (C40–C41/D16, 170/213)
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Diaphysis |
Myeloid |
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Epithelial |
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PNET/Ewing family |
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Metaphysis |
Osteoblast |
- Osteoid osteoma
- Osteoblastoma
- Osteoma/osteosarcoma
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Chondroblast |
- Chondroma/ecchondroma/enchondroma
- Enchondromatosis
- Extraskeletal chondroma
- Chondrosarcoma
- Mesenchymal chondrosarcoma
- Myxoid chondrosarcoma
- Osteochondroma
- Chondromyxoid fibroma
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Fibrous |
- (Peripheral) Ossifying fibroma
- Fibrosarcoma
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Epiphysis |
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Other/ungrouped |
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Index of bones and cartilage
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Description |
- Anatomy
- bones
- skull
- face
- neurocranium
- compound structures
- foramina
- upper extremity
- torso
- pelvis
- lower extremity
- Physiology
- Development
- Cells
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Disease |
- Congenital
- Neoplasms and cancer
- Trauma
- Other
- Symptoms and signs
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Treatment |
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Osteochondrodysplasia (Q77–Q78, 756.4–756.5)
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Osteodysplasia//
osteodystrophy |
Diaphysis |
- Camurati–Engelmann disease
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Metaphysis |
- Metaphyseal dysplasia
- Jansen's metaphyseal chondrodysplasia
- Schmid metaphyseal chondrodysplasia
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Epiphysis |
- Spondyloepiphyseal dysplasia congenita
- Multiple epiphyseal dysplasia
- Otospondylomegaepiphyseal dysplasia
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Osteosclerosis |
- Raine syndrome
- Osteopoikilosis
- Osteopetrosis
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Other/ungrouped |
- FLNB
- Opsismodysplasia
- Polyostotic fibrous dysplasia
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Chondrodysplasia/
chondrodystrophy
(including dwarfism) |
Osteochondroma |
- osteochondromatosis
- Hereditary multiple exostoses
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Chondroma/enchondroma |
- enchondromatosis
- Ollier disease
- Maffucci syndrome
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Growth factor receptor |
FGFR2: |
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FGFR3: |
- Achondroplasia
- Thanatophoric dysplasia
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COL2A1 collagen disease |
- Achondrogenesis
- Hypochondrogenesis
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SLC26A2 sulfation defect |
- Achondrogenesis
- Autosomal recessive multiple epiphyseal dysplasia
- Atelosteogenesis, type II
- Diastrophic dysplasia
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Chondrodysplasia punctata |
- Rhizomelic chondrodysplasia punctata
- Conradi–Hünermann syndrome
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Other dwarfism |
- Fibrochondrogenesis
- Short rib – polydactyly syndrome
- Majewski's polydactyly syndrome
- Léri–Weill dyschondrosteosis
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Index of bones and cartilage
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Description |
- Anatomy
- bones
- skull
- face
- neurocranium
- compound structures
- foramina
- upper extremity
- torso
- pelvis
- lower extremity
- Physiology
- Development
- Cells
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Disease |
- Congenital
- Neoplasms and cancer
- Trauma
- Other
- Symptoms and signs
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Treatment |
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External links