Chondrocalcinosis: Difference between revisions

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{{CMG}}; {{AE}} {{CZ}}


{{SK}} Pyrophosphate arthropathy; chondrocalcinosis; pseudogout; CPPD; Calcium pyrophosphate dihydrate deposition disease; CPPD disease
{{CMG}}; {{AE}} {{CZ}} {{LRO}} {{MAD}}
 
{{SK}}: Pyrophosphate arthropathy; chondrocalcinosis; pseudogout; CPPD; Calcium pyrophosphate dihydrate deposition disease; CPPD disease


==Overview==
==Overview==
'''Calcium pyrophosphate deposition disease''' ('''CPPD''') is a rheumatologic disorder with varied clinical manifestations due to precipitation of [[calcium pyrophosphate]] dihydrate crystals in the connective tissues. It is more commonly known by alternative names that specify certain clinical or radiographic findings, although neither is synonymous with CPPD. ''Pseudogout'' refers to the clinically evident acute [[synovitis]] with red, tender, and swollen joints that may resemble [[gout]]y arthritis (a similar condition with joint deposition of monosodium urate crystals). ''Chondrocalcinosis'', on the other hand, refers to the radiographic evidence of calcification in hyaline and/or fibrocartilage. ''Pyrophosphate arthropathy'' is a term that may refer to either of the above, but is uncommonly used.
Calcium pyrophosphate deposition disease (CPPD) is a rheumatologic disorder with varied clinical manifestations due to precipitation of [[calcium pyrophosphate]] dihydrate crystals in the connective tissues. It is more commonly known by alternative names that specify certain clinical or radiographic findings, although neither is synonymous with CPPD. ''Pseudogout'' refers to the clinically evident acute [[synovitis]] with red, tender, and swollen joints that may resemble [[gout]]y arthritis (a similar condition with joint deposition of monosodium urate crystals). ''Chondrocalcinosis'', on the other hand, refers to the radiographic evidence of calcification in hyaline and/or fibrocartilage. ''Pyrophosphate arthropathy'' is a term that may refer to either of the above, but is uncommonly used.


==Causes==
==Causes==
Line 24: Line 25:
===Life Threatening Causes===
===Life Threatening Causes===
*[[Wilson's disease ]]
*[[Wilson's disease ]]
===Causes by Organ System===
{|style="width:80%; height:100px" border="1"
|style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" |'''Cardiovascular'''
|style="height:100px"; style="width:75%" border="1" bgcolor="Beige" | No underlying causes
|-
|bgcolor="LightSteelBlue"| '''Chemical/Poisoning'''
|bgcolor="Beige"| [[Breakdown of adenosine triphosphate]]
|-
|-bgcolor="LightSteelBlue"
| '''Dental'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Dermatologic'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Drug Side Effect'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Ear Nose Throat'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Endocrine'''
|bgcolor="Beige"| [[Acromegaly]],  [[Growth hormone secreting pituitary adenoma]],  [[Hypophosphatemia]],  [[Hypothyroidism]]
|-
|-bgcolor="LightSteelBlue"
| '''Environmental'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Gastroenterologic'''
|bgcolor="Beige"| [[Wilson's disease ]]
|-
|-bgcolor="LightSteelBlue"
| '''Genetic'''
|bgcolor="Beige"| [[Alkaptonuria]],  [[Ochronosis]],  [[Wilson's disease ]]
|-
|-bgcolor="LightSteelBlue"
| '''Hematologic'''
|bgcolor="Beige"| [[Hemochromatosis]],  [[Hypercalcemia ]],  [[Hyperparathyroidism]],  [[Hypomagnesemia]],  [[Hypophosphatemia]]
|-
|-bgcolor="LightSteelBlue"
| '''Iatrogenic'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Infectious Disease'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Musculoskeletal/Orthopedic'''
|bgcolor="Beige"| [[Osteoarthritis]]
|-
|-bgcolor="LightSteelBlue"
| '''Neurologic'''
|bgcolor="Beige"| [[Hadd]]
|-
|-bgcolor="LightSteelBlue"
| '''Nutritional/Metabolic'''
|bgcolor="Beige"| [[Ochronosis]]
|-
|-bgcolor="LightSteelBlue"
| '''Obstetric/Gynecologic'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Oncologic'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Ophthalmologic'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Overdose/Toxicity'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Psychiatric'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Pulmonary'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Renal/Electrolyte'''
|bgcolor="Beige"| [[Oxalosis]]
|-
|-bgcolor="LightSteelBlue"
| '''Rheumatology/Immunology/Allergy'''
|bgcolor="Beige"| [[Arthritides]],  [[Familial chondrocalcinosis]],  [[Gout]],  [[Osteoarthritis]]
|-
|-bgcolor="LightSteelBlue"
| '''Sexual'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Trauma'''
|bgcolor="Beige"| [[Trauma]]
|-
|-bgcolor="LightSteelBlue"
| '''Urologic'''
|bgcolor="Beige"| No underlying causes
|-
|-bgcolor="LightSteelBlue"
| '''Miscellaneous'''
|bgcolor="Beige"| No underlying causes
|-
|}
===Causes in Alphabetical Order===
===Causes in Alphabetical Order===
{{columns-list|3|
{{columns-list|
*[[Acromegaly]]
*[[Acromegaly]]
*[[Alkaptonuria]]
*[[Alkaptonuria]]
Line 161: Line 47:
*[[Wilson's disease ]]
*[[Wilson's disease ]]
}}
}}
== Epidemiology ==
* [[Calcium pyrophosphate|Calcium pyrophosphate crystal]] deposition (CPPD) disease has been estimated to affect 4 to 7 percent of the adult populations of Europe and the United States. [7,8]
* The average age at diagnosis of CPPD disease in one study was 72 years [3].
* The [[prevalence]] of radiographic [[calcium pyrophosphate]] deposition according to age was:
65 to 74 years – 15 percent
75 to 84 years – 36 percent
>84 years – Almost 50 percent
* There is no major gender predominance in CPPD. Attacks of acute arthritis may occur more frequently in men.
== Pathogenesis ==
* [[Calcium pyrophosphate]] crystal formation reflects elevated levels of [[calcium]] or inorganic [[pyrophosphate]] in [[Cartilage|cartilages]] matrix.
* Excessive pyrophosphate levels arises from [[nucleoside]] triphosphate pyrophosphohydrolase [[enzyme]] overactivity.
* Increased concentrations of substrate ([[adenosine triphosphate]]) for this enzyme are also present in [[joint]] fluids from persons with CPPD.
* ''[[ANKH]]'' gene plays a role in formation of the crystals. There is now evidence that the ''ANKH'' gene product also promotes the release of ATP by chondrocytes. [14]
* One function of [[extracellular]] [[pyrophosphate]] appears to be to bind to and inhibit the growth of basic [[calcium phosphate]] crystals.
* In CPPD, excessive [[pyrophosphate]] levels arising from NTPPPH overactivity could provide the substrate for CPP crystal formation in the immediate environment of [[chondrocytes]].
* [[Mutations]] in or just upstream of the chromosome 5p locus of ''ANKH'' have also been identified in some individuals with idiopathic or sporadic CPPD deposition disease.
* Degenerative [[arthritis]] accompanying CPPD frequently involves such joints as the [[Metacarpophalangeal joint|metacarpophalangeal]] and wrist joints, which are commonly spared in classical [[osteoarthritis]].
</div>
</div>
==Clinical aspects==
CPPD crystal deposition disease is a polyarticular [[arthritis]] (i.e. it leads to an inflammation of several joints in the body), although it can initially present as monoarticular (i.e. confined to just one joint).


CPPD crystals tend to form within [[articular]] tissues. Diagnosis is by microscopy of fluid from a joint aspiration. Rhomboidal crystals should be seen under the microscope which exhibit weakly positive birefringence under polarized light.  [[X-ray]]s of the joint may show signs of chondrocalcinosis. Asymptomatic deposits can form in [[cartilage]], joint capsules, intervertebral discs, [[tendons]], and [[ligaments]]. Crystal deposition within cartilage (both [[hyaline]] and [[fibrocartilage]]) is known as chondrocalcinosis. Chondrocalcinosis initially is only visible microscopically, but if there is enough calcification, we can seen it [[radiographic]]ally as well. Common locations of chondrocalcinosis include the knees, wrists, elbows, and hips.
==Clinical presentation==
* '''Asymptomatic CPPD disease''': Most joints in which CPP crystal deposition is readily apparent on radiographs are asymptomatic, even among patients in whom acute or chronic clinical manifestations of CPPD disease in one or several other joints have occurred.
* '''Acute CPP crystal arthritis''': The [[knee]] is affected in over 50 percent of all acute attacks of acute CPP crystal arthritis. Other joints typically affected in acute CPP crystal [[arthritis]] include wrists, shoulders, ankles, feet, and elbows. Predisposing factors include [[trauma]], [[surgery]], or severe medical illness often provoke acute attacks. Treatment with [[pamidronate]] or [[Granulocyte-macrophage colony-stimulating factor|granulocyte-macrophage-colony-stimulating factor]] have also been reported to precipitate acute attacks of pseudogout.
* '''Chronic CPP crystal inflammatory arthritis''': the chronic inflammatory arthritis of CPPD disease involves multiple joints, frequently involving peripheral joints of the upper and lower extremities, including the wrists and metacarpophalangeal joints, as well as the knees and elbows, in a symmetric or nearly symmetric pattern. Chronic CPP crystal inflammatory arthritis occurs in 5 percent or less of patients with symptomatic CPPD disease.
* '''Severe joint degeneration''': Neuropathic arthropathy is characterized by severe joint degeneration and disruption occurring in the course of neurologic disorders leading to joint denervation; the affected joint is often called a [[Charcot joint]].
* Underlying disorders associated with Charcot joints include [[diabetes mellitus]], [[Tabes Dorsalis|tabes dorsalis]], and [[syringomyelia]].
* '''Spinal involvement''': CPP crystal deposition in and about the spine has been associated with a number of clinical manifestations, including spine [[stiffness]], sometimes associated with bony [[ankylosis]], which can resemble the spinal changes of [[ankylosing spondylitis]] or diffuse idiopathic skeletal [[hyperostosis]].  


Crystal-induced [[synovitis]] is the result of shedding of crystals in the joint space after rupture of a CPPD deposit. Clinically this presents as an acute inflammatory synovitis very similar to that of an attack of gout, and has been referred to as "pseudogout."
== Diagnosis ==
* [[Synovial fluid]]: Identification of CPP crystals is diagnostic. Successful identification of the crystals diminishes as the time between joint aspiration and microscopic examination increases.  


*Other conditions associated with chondrocalcinosis:
===Radiological findings===
**[[Wikibooks:Diagnostic Radiology/Musculoskeletal Imaging/Metabolic Basic/Primary hyperparathyroidism|hyperparathyroidism]]
**[[hemochromatosis]]
**[[hypophosphatemia]]
**[[Renal osteodystrophy]]
 
==Radiologic findings==
Three main manifestations of CPPD deposition:  
Three main manifestations of CPPD deposition:  


#chondrocalcinosis
#[[Chondrocalcinosis]]
#crystal induced synovitis (pseudogout syndrome)
#Crystal induced [[synovitis]]
#pyrophosphate arthropathy
#[[pyrophosphate arthropathy]]
'''Plain film radiography'''
* [[Cartilage]]: CPP crystal deposits in [[hyaline]] cartilage frequently appear as a radiopaque line paralleling the surface of the underlying [[bone]].
* [[Joints]]: Larger joints are frequently involved in CPPD disease. Synovial [[calcification]] is often fainter and more diffuse than [[cartilage]] calcification. Linear calcifications involving the [[Achilles tendon]] or [[plantar fascia]]. [32].
'''Degenerative changes'''
* CPP crystal deposition is often associated with degenerative changes in joints. It includes subchondral cysts, [[osteophyte]] formation, and bone and cartilage fragmentation.
* Radiographic features of [[osteoarthritis]]
* [[Stress fracture|Stress fractures]] or [[osteonecrosis]] ([[avascular necrosis]])
[[File:Case courtesy of A.Prof Frank Gaillard, Radiopaedia.org, rID 35840.jpg|center|300px|thumb|Pseuogout in knee, source: File:Case courtesy of A.Prof Frank Gaillard, Radiopaedia.org, rID 35840.jpg]]


==Treatment==
[[File:Case courtesy of Dr Charlie Chia-Tsong Hsu, Radiopaedia.org, rID 31099.jpg|300px|center|thumb|Pseudogout in knee, source: File:Case courtesy of Dr Charlie Chia-Tsong Hsu, Radiopaedia.org, rID 31099.jpg]]


Treatment of CPPD is mostly aimed at preventing further crystal formation and reducing symptoms from crystal deposition. CPPD crystal deposition cannot be reversed. If CPPD results from underlying metabolic abnormalities ([[Wikibooks:Diagnostic Radiology/Musculoskeletal Imaging/Metabolic Basic/Primary hyperparathyroidism|hyperparathyroidism]], [[hemochromatosis]], [[hypophosphatasia]], or [[hypomagnesemia]])<ref>Wright G.D., Doherty M. Calcium pyrophosphate crystal deposition is not always 'wear and tear' or aging. Ann Rheum Dis.1997; 56: 586-588 PMID 9389218</ref>, these can be treated directly.
[[File:Case courtesy of Dr Erik Ranschaert, Radiopaedia.org, rID 12443.jpg|300px|center|thumb|Pseudogout in spines, source: File:Case courtesy of Dr Erik Ranschaert, Radiopaedia.org, rID 12443.jpg]]


For symptomatic joints, treatment is similar to treatment of gout. When a single joint is involved, joint aspiration and intra-articular corticosteroid injection is often used, in addition to [[Non-steroidal anti-inflammatory drug|NSAIDs]] and/or [[colchicine]]. When multiple joints are involved, joint injection is often impractical, or limited only to the most severely involved joint, and oral systemic treatment is chosen instead.
'''Ultrasonographic findings'''


Because pyrophosphate complexes with magnesium prior to its degradation <ref>Wright G.D., Doherty M. Calcium pyrophosphate crystal deposition is not always 'wear and tear' or aging. Ann Rheum Dis.1997; 56: 586-588 PMID 9389218</ref>, and CPPD can result from pathologically low magnesium levels, magnesium supplementation may be of help, particularly in a few patients with underlying hypomagnesemia. It may be possible to end attacks by ingesting large (maximum RDA) doses of magnesium supplement accompanied by [[vitamin B6]] to help absorption. What that does is assist the body in re-dissolving the calcium in the joint fluid, and with maintenance doses, often in the form of snacking on magnesium-rich foods such as almonds, further attacks can be prevented altogether - without medication.
The following findings on [[ultrasonography]] of articular and fibrocartilage:
 
* A thin hyperechoic band paralleling the bone cortex and separated from it by a hypoechoic region representing cartilage.
==References==
* Small hyperechoic rounded amorphous shaped regions which are most often found in images of fibrocartilage of the wrist and menisci of the knee, and in tendons.
{{reflist|2}}
* Nodular hyperechoic deposits in bursae and articular recesses.
* Hyperechoic lines of calcification running parallel to tendon fibers.


{{Diseases of the musculoskeletal system and connective tissue}}
== Differential diagnosis ==
'''Acute arthritis'''


[[Category:Arthritis]]
Pseudogout acute attacks should be differentiated from other causes of acute monoarthritis such as:
[[Category:Rheumatology]]
* [[Infection]]


* [[Fracture of bone|Fracture]]
* [[Osteonecrosis]]
* [[Meniscal tear]]
* Plant thorn [[synovitis]]
'''Chronic inflammatory arthritis'''


[[de:Pseudogicht]]
Chronic CPP inflammatory arthritis should be differentiated from other forms of chronic inflammatory arthritis such as:
[[ja:偽痛風]]
* [[Rheumatoid arthritis]]
[[sv:Pyrofosfatsynovit]]
* [[Spondyloarthritis]]
* [[Systemic lupus erythematosus]]
* [[Sarcoidosis]]
* [[Osteoarthritis]]
* Peripheral [[spondyloarthritis]], including [[reactive arthritis]] and arthritis associated with [[inflammatory bowel disease]], as well as [[psoriatic arthritis]].
Tumors such as:
* Tenosynovial [[Giant cell tumor of bone|giant cell tumor]]
* [[Chondrosarcoma]]
* [[Osteoid osteoma]]


== Treatment ==
* Treatment of CPPD is mostly aimed at preventing further crystal formation and reducing symptoms from crystal deposition. CPPD crystal deposition cannot be reversed. If CPPD results from underlying metabolic abnormalities ([[Wikibooks:Diagnostic Radiology/Musculoskeletal Imaging/Metabolic Basic/Primary hyperparathyroidism|hyperparathyroidism]], [[hemochromatosis]], [[hypophosphatasia]], or [[hypomagnesemia]])<ref>Wright G.D., Doherty M. Calcium pyrophosphate crystal deposition is not always 'wear and tear' or aging. Ann Rheum Dis.1997; 56: 586-588 PMID 9389218</ref>, these can be treated directly.
* Treatment is similar to the treatment of [[gout]]. When a single joint is involved, joint aspiration and intra-articular [[corticosteroid]] injection is often used, in addition to [[Non-steroidal anti-inflammatory drug|NSAIDs]] and/or [[colchicine]]. When multiple joints are involved, joint injection is often impractical, or limited only to the most severely involved joint, and oral systemic treatment is chosen instead.
* Because [[pyrophosphate]] complexes with [[magnesium]] prior to its degradation <ref>Wright G.D., Doherty M. Calcium pyrophosphate crystal deposition is not always 'wear and tear' or aging. Ann Rheum Dis.1997; 56: 586-588 PMID 9389218</ref>, and CPPD can result from pathologically low magnesium levels, magnesium supplementation may be of help, particularly in a few patients with underlying hypomagnesemia. It may be possible to end attacks by ingesting large (maximum RDA) doses of magnesium supplement accompanied by [[vitamin B6]] to help absorption. What that does is assist the body in re-dissolving the calcium in the joint fluid, and with maintenance doses, often in the form of snacking on magnesium-rich foods such as almonds, further attacks can be prevented altogether - without medication.
* [[Anti inflammatory medications|Anti-inflammatory medication]], usually by intraarticular injection, supported by local measures to reduce symptoms.
* Joint fluid aspiration and [[glucocorticoid]] injection usually provide relief in pain and swelling within 8 to 24 hours.
* Application of ice or cool packs and immobilization and resting of the joint by restriction of weight bearing.
* systemic anti-inflammatory therapy is warranted, employing agents typically used for the treatment of acute gout.
* These include: [[NSAIDs]], which may, however, be contraindicated in older adults, the population especially susceptible to acute attacks of pseudogout.
* [[Colchicine]], which is particularly useful if a low-dose regimen is initiated within hours of attack onset;
* glucocorticoids, which are efficacious in patients unable to take NSAIDs or colchicine.
* In patients in whom treatment for acute CPP crystal arthritis is initiated within about 24 hours of onset and whose clinical and concomitant medication profiles permit its consideration, we suggest oral [[colchicine]] in a low-dose regimen as initially recommended for the treatment of [[Acute gouty arthritis|acute gout]], rather than using oral [[glucocorticoids]].
* For regimens using low-dose [[colchicine]], followed by 0.6 mg colchicine taken twice daily until the attack abates. Common adverse effects of [[colchicine]] may include [[diarrhea]] and abdominal [[cramping]], but these are less likely in patients who receive no more than 1.8 mg in total on the first day compared with patients receiving higher doses, such as 0.6 mg every one to two hours until symptom relief or intolerance.
* In patients in whom [[glucocorticoid]] therapy is inadequate, it is important to confirm the absence of [[hepatic]] disease that might impair the conversion of [[prednisone]] to [[prednisolone]], in which case the [[glucocorticoid]] therapy can be switched to oral prednisolone.
* An alternative option is managing the symptoms using supportive measures until they resolve with analgesics, rest, splinting, and icing.


{{WikiDoc Help Menu}}
==References==
{{WikiDoc Sources}}
{{reflist|2}}
{{WH}}
{{WS}}
<references />

Latest revision as of 20:33, 10 January 2020

Chondrocalcinosis
Chondrocalcinosis of the articular and fibrocartilage of the left knee in a patient with calcium pyrophosphate dihydrate deposition disease (CPPD)
ICD-10 M11.1-M11.2
ICD-9 712.3
DiseasesDB 10832
MedlinePlus 000421
MeSH D002805

Template:Search infobox

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2] Luke Rusowicz-Orazem, B.S. Mohammed Abdelwahed M.D[3]

Synonyms and keywords:: Pyrophosphate arthropathy; chondrocalcinosis; pseudogout; CPPD; Calcium pyrophosphate dihydrate deposition disease; CPPD disease

Overview

Calcium pyrophosphate deposition disease (CPPD) is a rheumatologic disorder with varied clinical manifestations due to precipitation of calcium pyrophosphate dihydrate crystals in the connective tissues. It is more commonly known by alternative names that specify certain clinical or radiographic findings, although neither is synonymous with CPPD. Pseudogout refers to the clinically evident acute synovitis with red, tender, and swollen joints that may resemble gouty arthritis (a similar condition with joint deposition of monosodium urate crystals). Chondrocalcinosis, on the other hand, refers to the radiographic evidence of calcification in hyaline and/or fibrocartilage. Pyrophosphate arthropathy is a term that may refer to either of the above, but is uncommonly used.

Causes

Life Threatening Causes

Causes in Alphabetical Order

Epidemiology

  • Calcium pyrophosphate crystal deposition (CPPD) disease has been estimated to affect 4 to 7 percent of the adult populations of Europe and the United States. [7,8]
  • The average age at diagnosis of CPPD disease in one study was 72 years [3].
  • The prevalence of radiographic calcium pyrophosphate deposition according to age was:

65 to 74 years – 15 percent

75 to 84 years – 36 percent

>84 years – Almost 50 percent

  • There is no major gender predominance in CPPD. Attacks of acute arthritis may occur more frequently in men.

Pathogenesis

  • Calcium pyrophosphate crystal formation reflects elevated levels of calcium or inorganic pyrophosphate in cartilages matrix.
  • Excessive pyrophosphate levels arises from nucleoside triphosphate pyrophosphohydrolase enzyme overactivity.
  • Increased concentrations of substrate (adenosine triphosphate) for this enzyme are also present in joint fluids from persons with CPPD.
  • ANKH gene plays a role in formation of the crystals. There is now evidence that the ANKH gene product also promotes the release of ATP by chondrocytes. [14]
  • One function of extracellular pyrophosphate appears to be to bind to and inhibit the growth of basic calcium phosphate crystals.
  • In CPPD, excessive pyrophosphate levels arising from NTPPPH overactivity could provide the substrate for CPP crystal formation in the immediate environment of chondrocytes.
  • Mutations in or just upstream of the chromosome 5p locus of ANKH have also been identified in some individuals with idiopathic or sporadic CPPD deposition disease.
  • Degenerative arthritis accompanying CPPD frequently involves such joints as the metacarpophalangeal and wrist joints, which are commonly spared in classical osteoarthritis.

Clinical presentation

  • Asymptomatic CPPD disease: Most joints in which CPP crystal deposition is readily apparent on radiographs are asymptomatic, even among patients in whom acute or chronic clinical manifestations of CPPD disease in one or several other joints have occurred.
  • Acute CPP crystal arthritis: The knee is affected in over 50 percent of all acute attacks of acute CPP crystal arthritis. Other joints typically affected in acute CPP crystal arthritis include wrists, shoulders, ankles, feet, and elbows. Predisposing factors include trauma, surgery, or severe medical illness often provoke acute attacks. Treatment with pamidronate or granulocyte-macrophage-colony-stimulating factor have also been reported to precipitate acute attacks of pseudogout.
  • Chronic CPP crystal inflammatory arthritis: the chronic inflammatory arthritis of CPPD disease involves multiple joints, frequently involving peripheral joints of the upper and lower extremities, including the wrists and metacarpophalangeal joints, as well as the knees and elbows, in a symmetric or nearly symmetric pattern. Chronic CPP crystal inflammatory arthritis occurs in 5 percent or less of patients with symptomatic CPPD disease.
  • Severe joint degeneration: Neuropathic arthropathy is characterized by severe joint degeneration and disruption occurring in the course of neurologic disorders leading to joint denervation; the affected joint is often called a Charcot joint.
  • Underlying disorders associated with Charcot joints include diabetes mellitus, tabes dorsalis, and syringomyelia.
  • Spinal involvement: CPP crystal deposition in and about the spine has been associated with a number of clinical manifestations, including spine stiffness, sometimes associated with bony ankylosis, which can resemble the spinal changes of ankylosing spondylitis or diffuse idiopathic skeletal hyperostosis.

Diagnosis

  • Synovial fluid: Identification of CPP crystals is diagnostic. Successful identification of the crystals diminishes as the time between joint aspiration and microscopic examination increases.

Radiological findings

Three main manifestations of CPPD deposition:

  1. Chondrocalcinosis
  2. Crystal induced synovitis
  3. pyrophosphate arthropathy

Plain film radiography

Degenerative changes

Pseuogout in knee, source: File:Case courtesy of A.Prof Frank Gaillard, Radiopaedia.org, rID 35840.jpg
Pseudogout in knee, source: File:Case courtesy of Dr Charlie Chia-Tsong Hsu, Radiopaedia.org, rID 31099.jpg
Pseudogout in spines, source: File:Case courtesy of Dr Erik Ranschaert, Radiopaedia.org, rID 12443.jpg

Ultrasonographic findings

The following findings on ultrasonography of articular and fibrocartilage:

  • A thin hyperechoic band paralleling the bone cortex and separated from it by a hypoechoic region representing cartilage.
  • Small hyperechoic rounded amorphous shaped regions which are most often found in images of fibrocartilage of the wrist and menisci of the knee, and in tendons.
  • Nodular hyperechoic deposits in bursae and articular recesses.
  • Hyperechoic lines of calcification running parallel to tendon fibers.

Differential diagnosis

Acute arthritis

Pseudogout acute attacks should be differentiated from other causes of acute monoarthritis such as:

Chronic inflammatory arthritis

Chronic CPP inflammatory arthritis should be differentiated from other forms of chronic inflammatory arthritis such as:

Tumors such as:

Treatment

  • Treatment of CPPD is mostly aimed at preventing further crystal formation and reducing symptoms from crystal deposition. CPPD crystal deposition cannot be reversed. If CPPD results from underlying metabolic abnormalities (hyperparathyroidism, hemochromatosis, hypophosphatasia, or hypomagnesemia)[1], these can be treated directly.
  • Treatment is similar to the treatment of gout. When a single joint is involved, joint aspiration and intra-articular corticosteroid injection is often used, in addition to NSAIDs and/or colchicine. When multiple joints are involved, joint injection is often impractical, or limited only to the most severely involved joint, and oral systemic treatment is chosen instead.
  • Because pyrophosphate complexes with magnesium prior to its degradation [2], and CPPD can result from pathologically low magnesium levels, magnesium supplementation may be of help, particularly in a few patients with underlying hypomagnesemia. It may be possible to end attacks by ingesting large (maximum RDA) doses of magnesium supplement accompanied by vitamin B6 to help absorption. What that does is assist the body in re-dissolving the calcium in the joint fluid, and with maintenance doses, often in the form of snacking on magnesium-rich foods such as almonds, further attacks can be prevented altogether - without medication.
  • Anti-inflammatory medication, usually by intraarticular injection, supported by local measures to reduce symptoms.
  • Joint fluid aspiration and glucocorticoid injection usually provide relief in pain and swelling within 8 to 24 hours.
  • Application of ice or cool packs and immobilization and resting of the joint by restriction of weight bearing.
  • systemic anti-inflammatory therapy is warranted, employing agents typically used for the treatment of acute gout.
  • These include: NSAIDs, which may, however, be contraindicated in older adults, the population especially susceptible to acute attacks of pseudogout.
  • Colchicine, which is particularly useful if a low-dose regimen is initiated within hours of attack onset;
  • glucocorticoids, which are efficacious in patients unable to take NSAIDs or colchicine.
  • In patients in whom treatment for acute CPP crystal arthritis is initiated within about 24 hours of onset and whose clinical and concomitant medication profiles permit its consideration, we suggest oral colchicine in a low-dose regimen as initially recommended for the treatment of acute gout, rather than using oral glucocorticoids.
  • For regimens using low-dose colchicine, followed by 0.6 mg colchicine taken twice daily until the attack abates. Common adverse effects of colchicine may include diarrhea and abdominal cramping, but these are less likely in patients who receive no more than 1.8 mg in total on the first day compared with patients receiving higher doses, such as 0.6 mg every one to two hours until symptom relief or intolerance.
  • In patients in whom glucocorticoid therapy is inadequate, it is important to confirm the absence of hepatic disease that might impair the conversion of prednisone to prednisolone, in which case the glucocorticoid therapy can be switched to oral prednisolone.
  • An alternative option is managing the symptoms using supportive measures until they resolve with analgesics, rest, splinting, and icing.

References

  1. Wright G.D., Doherty M. Calcium pyrophosphate crystal deposition is not always 'wear and tear' or aging. Ann Rheum Dis.1997; 56: 586-588 PMID 9389218
  2. Wright G.D., Doherty M. Calcium pyrophosphate crystal deposition is not always 'wear and tear' or aging. Ann Rheum Dis.1997; 56: 586-588 PMID 9389218

Template:WH Template:WS