- Neuropathic arthropathy
"Charcot joint disease" redirects here. For the nerve disease, see Charcot-Marie-Tooth disease. For Charcot's disease (Lou Gehrig's disease), see Amyotrophic lateral sclerosis.For several other diseases associated with Jean-Martin Charcot, see Jean-Martin Charcot.
Neuropathic joint disease Classification and external resources
A 68-year-old diabetic female on dialysis presented with a chronic right heel ulcer (3.4 cm X 3.1 cm) of greater than 3 months duration. Photograph of the wound after thorough wound bed preparation over the course of 2 weeks.
ICD-10 M14.6 ICD-9 713.5 DiseasesDB 2344 eMedicine orthoped/381 radio/476
Neuropathic arthropathy (or neuropathic osteoarthropathy), also known as Charcot joint (often "Charcot foot"), refers to progressive degeneration of a weight bearing joint, a process marked by bony destruction, bone resorption, and eventual deformity. Onset is usually insidious.
If this pathological process continues unchecked, it could result in joint deformity, ulceration and/or superinfection, loss of function, and in the worst case scenario: amputation or death. Early identification of joint changes is the best way to limit morbidity.
Any condition resulting in decreased peripheral sensation, proprioception, and fine motor control:
- Diabetes mellitus neuropathy (the most common in the U.S. today, resulting in destruction of foot and ankle joints), with Charcot joints in 1/600-700 diabetics. Related to long-term poor glucose control.
- Alcoholic neuropathy
- Cerebral palsy
- Syphilis (tabes dorsalis), caused by the organism Treponema pallidum
- Spinal cord injury
- Intra-articular steroid injections
- Congenital insensitivity to pain
- Two primary theories have been advanced:
- Neurotrauma: Loss of peripheral sensation and proprioception leads to repetitive microtrauma to the joint in question; this damage goes unnoticed by the neuropathic patient, and the resultant inflammatory resorption of traumatized bone renders that region weak and susceptible to further trauma. Indeed, it is a vicious cycle. In addition, poor fine motor control generates unnatural pressure on certain joints, leading to additional microtrauma.
- Neurovascular: Neuropathic patients have dysregulated autonomic nervous system reflexes, and de-sensitized joints receive significantly greater blood flow. The resulting hyperemia leads to increased osteoclastic resorption of bone, and this, in concert with mechanical stress, leads to bony destruction.
In reality, both of these mechanisms probably play a role in the development of a Charcot joint.
Diabetes is the foremost cause in America today for neuropathic joint disease, and the foot is the most affected region. In those with foot deformity, approximately 60% are in the tarsometatarsal joints (medial joints affected more than lateral), 30% Metatarsophalangeal joints and 10% have ankle disease. Over half of diabetic patients with neuropathic joints can recall some kind of precipitating trauma, usually, minor.
Patients with neurosyphilis tend to have knee involvement, and patients with syringomyelia of the spinal cord may demonstrate shoulder deformity.
Hip joint destruction is also seen in neuropathic patients.
Clinical findings include erythema, edema and increased temperature in the affected joint. In neuropathic foot joints, plantar ulcers may be present. Note that it is often difficult to differentiate osteomyelitis from a Charcot joint, as they may have similar tagged WBC scan and MRI features (joint destruction, dislocation, edema). Definitive diagnosis may require bone or synovial biopsy.
First, it is important to recognize that two types of abnormality may be detected. One is termed atrophic, in which there is osteolysis of the distal metatarsals in the forefoot. The more common form of destruction is hypertrophic joint disease, characterized by acute peri-articular fracture and joint dislocation. According to Yochum and Rowe, the "6 D's" of hypertrophy are:
- Distended joint
- Density increase
- Debris production
The natural history of the joint destruction process has a classification scheme of its own, offered by Eichenholtz decades ago:
Stage 0: Clinically, there is joint edema, but radiographs are negative. Note that a bone scan may be positive before a radiograph is, making it a sensitive but not very specific modality.
Stage 1: Osseous fragmentation with joint dislocation seen on radiograph ("acute Charcot").
Stage 2: Decreased local edema, with coalescence of fragments and absorption of fine bone debris
Stage 3: No local edema, with consolidation and remodeling (albeit deformed) of fracture fragments. The foot is now stable.
Destroyed Tarsometatarsal joints in the medial left foot, with fracture and dislocation of fragments; these are classic findings. Also note loss of the foot arch and acquired flat foot (pes planus) deformity.
- "Licked candy stick" appearance, commonly seen at the distal aspect of the metatarsals
- Diabetic osteolysis
- Bone resorption
Once the process is recognized, immobilization with a total contact cast will help ward off further joint destruction. Pneumatic walking braces are also used. Surgical correction of a joint is rarely successful in the long-term in these patients.
It can take 6–9 months for the edema and erythema of the affected joint to recede.
- Neuropathic osteoarthropathy by Monica Bhargava, M.D., University of Washington Department of Radiology
- John R. Crockarell; Daugherty, Kay; Jones, Linda Winstead; Frederick M. Azar; Beaty, James H; James H. Calandruccio; Peter G. Carnesale; Kevin B. Cleveland; Andrew H. Crenshaw (2003). Campbell's Operative Orthopedics (10th ed.). Saint Louis: C.V. Mosby. ISBN 0-323-01248-5.
- Gupta R (November 1993). "A short history of neuropathic arthropathy". Clin. Orthop. Relat. Res. (296): 43–9. PMID 8222448.
- Sommer TC, Lee TH (November 2001). "Charcot foot: the diagnostic dilemma". Am Fam Physician 64 (9): 1591–8. PMID 11730314.
Musculoskeletal disorders: Arthropathies (M00–M19, 711–719) Arthritis
polyarthritis)Septic arthritis · Tuberculosis arthritis · Reactive arthritis (indirectly)NoninfectiousSeronegative spondyloarthropathy: Reactive arthritis · Psoriatic arthritis · Ankylosing spondylitisRheumatoid arthritis: Juvenile idiopathic arthritis · Adult-onset Still's disease · Felty's syndromeNoninflammatory
Otherhemorrhage (Hemarthrosis) · pain (Arthralgia) · Osteophyte · villonodular synovitis (Pigmented villonodular synovitis) · Joint stiffness
anat(h/c, u, t, l)/phys
noco(arth/defr/back/soft)/cong, sysi/epon, injr
proc, drug(M01C, M4)
Diabetes (E10–E14, 250) Types of diabetesPrediabetes (Impaired fasting glucose, Impaired glucose tolerance) Blood testsBlood sugar · Glycosylated hemoglobin · Glucose tolerance test · Fructosamine Diabetes managementDiabetic diet · Anti-diabetic drugs · Insulin therapy · Glossary of diabetes Complications/prognosisDiabetic comas (Diabetic hypoglycemia, Diabetic ketoacidosis, Nonketotic hyperosmolar) · Diabetic angiopathy · Diabetic foot (ulcer, neuropathic arthropathy) · Diabetic myonecrosis · Diabetic nephropathy · Diabetic neuropathy · Diabetic retinopathy · Diabetic cardiomyopathy · Diabetic dermadrome (Diabetic dermopathy, Diabetic bulla, Diabetic cheiroarthropathy, Neuropathic ulcer) Lines of researchCategories:
- Inflammatory polyarthropathies
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