Paget disease of bone

骨パジェット病

WordNet

1. an impairment of health or a condition of abnormal functioning
2. remove the bones from; "bone the turkey before roasting it" (同)debone
3. the porous calcified substance from which bones are made (同)osseous_tissue
4. consisting of or made up of bone; "a bony substance"; "the bony framework of the body"
5. a shade of white the color of bleached bones (同)ivory, pearl, off-white
6. rigid connective tissue that makes up the skeleton of vertebrates (同)os
7. having bones as specified; "his lanky long-boned body"
8. having had the bones removed; "a boneless rib roast"; "a boned (or deboned) fish" (同)deboned
9. caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological

PrepTutorEJDIC

1. 《所有・所属》…『の』,…のものである,…に属する・《材料・要素》…『でできた』,から成る・《部分》…『の』[『中の』] ・《数量・単位・種類を表す名詞に付いて》…の・《原因・動機》…『で』,のために(because of) ・《主格関係》…『の』,による,によって・《目的格関係》…『を』,の・《同格関係》…『という』・《関係・関連》…『についての』[『の』],の点で・《抽象名詞などと共に》…の[性質をもつ] ・《『It is』+『形』+『of』+『名』+『to』 doの形で,ofの後の名詞を意味上の主語として》・《分離》…『から』・《起原・出所》…『から』[『の』](out of) ・《『名』+『of』+『a』(『an』)+『名』の形で》…のような・《『名』+『of』+『mine』(『yours, his』など独立所有格)の形で》…の…・《時》(1)《副詞句を作って》…に《形容詞句を作って》…の・《時刻》《米》…前(to,《米》before)
2. (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
3. 女性の話術芸人 =diseur
4. 〈C〉骨 / 〈U〉骨を作っている物質,骨質 / 《複数形で》骨格;死骸(がい) / 〈魚など〉‘の'骨を取る
5. (魚など)骨を取り除いた / (衣服が)(コルセットなどで)骨で張りをつけた[ような]
6. 病気にかかった / 病的な,不健全な(morbid)

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/10/18 10:35:56」(JST)

wiki en

[Wiki en表示]

For other diseases named after Paget, see Paget's disease (disambiguation).

Paget's disease of bone
Classification and external resources
"This 92 year-old male patient presented for assessment of acute hemiparesis. An incidental finding was marked thickening of the calvarium. The diploic space is widened and there are ill-defined sclerotic and lucent areas throughout. The cortex is thickened and irregular. The findings probably correspond to the “cotton wool spots” seen on plain films in the later stages of Paget’s disease."
ICD-10	M88
ICD-9	731.0
OMIM	602080
DiseasesDB	9479
MedlinePlus	000414
eMedicine	med/2998 radio/514 pmr/98
MeSH	D010001

The Ugly Duchess - portrait by Quentin Matsys. Based on a woman suffering from a rare form of Paget's disease of bone.

Paget's disease of bone is a chronic disorder that can result in enlarged and misshapen bones. The excessive breakdown and formation of bone tissue causes affected bone to weaken, resulting in pain, misshapen bones, fractures, and arthritis in the joints near the affected bones. Paget's disease typically is localized, affecting just one or a few bones, as opposed to osteoporosis, for example, which usually affects all the bones in the body. Decisions about treating Paget's disease can be complicated because 1) no two people are affected in exactly the same way by the disease, and 2) it is sometimes difficult to predict whether a person with Paget's disease who shows no signs of the disorder will develop symptoms or complications (such as a bone fracture) at a later date. Although there is no cure for Paget's disease, medications (bisphosphonates and calcitonin) can help control the disorder and lessen pain and other symptoms. Paget's disease experts recommend that these medications be taken by people with Paget's disease who

• have bone pain, headache, back pain, or a nerve-related symptom (such as "shooting" pains in the leg) that is directly associated with the disease;
• have elevated levels of serum alkaline phosphatase (SAP) in their blood;
• display evidence that a bone fracture will occur;
• require pretreatment therapy for affected bones that require surgery;
• have active symptoms in the skull, long bones, or vertebrae (spine);
• have the disease in bones located next to major joints, placing them at risk of developing osteoarthritis;
• develop hypercalcemia that occurs when a person with several bones affected by Paget's disease and a high serum alkaline phosphtase level is immobilized.

Today's medications, especially when started before complications begin, are often successful in controlling the disorder. Paget's disease is rarely diagnosed in people less than 40 years of age. Men are more commonly affected than women (3:2). Prevalence of Paget's disease ranges from 1.5 to 8.0 percent, depending on age and country of residence. Prevalence of familial Paget's disease (where more than one family member has the disease) ranges from 10 to 40 percent in different parts of the world.^{[citation needed]} Because early diagnosis and treatment is important, after age 40, siblings and children of someone with Paget's disease may wish to have an alkaline phosphatase blood test every two or three years. If the alkaline phosphatase level is above normal, other tests such as a bone-specific alkaline phosphatase test, bone scan, or X-ray can be performed.

Etymology

The term osteitis deformans is now considered technically incorrect, and the preferred term is osteodystrophia deformans.

Causes

Viral

Paget's disease may be caused by a slow virus infection (i.e., paramyxoviruses) present for many years before symptoms appear.

• Measles, though recent evidence has cast some doubt upon the measles association.

• Canine distemper virus

• Respiratory syncytial virus

Contamination has been suggested to have played a role in producing past positive results.

Genetic

There is also a hereditary factor. Associations include:

Name	OMIM	Locus	Gene
PDB1	167250	6p	?
PDB2		18q22.1	RANK
PDB3		5q35	SQSTM1
PDB4	606263	5q31	?

Pathogenesis

Micrograph showing Paget's disease of the bone with the characteristic jigsaw puzzle-like/mosaic pattern, H&E stain

The pathogenesis of Paget's disease is described in 4 stages:

1. Osteoclastic activity
   
2. Mixed osteoclastic - osteoblastic activity
   
3. Osteoblastic activity
   
4. Malignant degeneration
   

Initially, there is a marked increase in the rate of bone resorption at localized areas caused by large and numerous osteoclasts. These localized areas of osteolysis are seen radiologically as an advancing lytic wedge in long bones or osteoporosis circumscripta in the skull. The osteolysis is followed by a compensatory increase in bone formation induced by osteoblasts recruited to the area. This is associated with accelerated deposition of lamellar bone in a disorganized fashion. This intense cellular activity produces a chaotic picture of trabecular bone ("mosaic" pattern), rather than the normal linear lamellar pattern. The resorbed bone is replaced and the marrow spaces are filled by an excess of fibrous connective tissue with a marked increase in blood vessels, causing the bone to become hypervascular. The bone hypercellularity may then diminish, leaving a dense "pagetic bone," also known as burned-out Paget's disease.

Sir James Paget first suggested the disease was due to an inflammatory process. New evidence suggests he may have been correct and that a paramyxovirus infection is the underlying cause of Paget's disease.^{[citation needed]} No infectious virus has yet been isolated as a causative agent, however, and other evidence suggests an intrinsic hyperresponsive reaction to vitamin D and RANK ligand is the cause.^{[citation needed]} Further research is therefore necessary.

Symptoms

Many patients do not know they have Paget's disease because they have a mild case with no symptoms. Sometimes, symptoms may be confused with those of arthritis or other disorders. In other cases, the diagnosis is made only after complications have developed. Symptoms can include:

• Bone pain

Diagnosis

Paget's disease may be diagnosed using one or more of the following tests:

• Pagetic bone has a characteristic appearance on X-rays. A skeletal survey is therefore indicated.
• An elevated level of alkaline phosphatase in the blood in combination with normal calcium, phosphate, and aminotransferase levels in an elderly patient are suggestive of Paget's disease.
• Elevated levels of serum and urinary hydroxyproline are also found.
• Bone scans are useful in determining the extent and activity of the condition. If a bone scan suggests Paget's disease, the affected bone(s) should be X-rayed to confirm the diagnosis.

Comparison of bone pathology

Condition	Calcium	Phosphate	Alkaline phosphatase	Parathyroid hormone	Comments
Osteoporosis	unaffected	unaffected	variable	unaffected	decreased bone mass
Osteopetrosis	unaffected	unaffected	elevated	unaffected	thick dense bones also known as marble bone
Osteomalacia and rickets	decreased	decreased	variable	elevated	soft bones
Osteitis fibrosa cystica	elevated	decreased	elevated	elevated	brown tumors
Paget's disease of bone	unaffected	unaffected	variable (depending on stage of disease)	unaffected	abnormal bone architecture

Prognosis

The outlook is generally good, particularly if treatment is given before major changes in the affected bones have occurred. Any bone or bones can be affected, but Paget's disease occurs most frequently in the spine, skull, pelvis, femur, and lower legs. In general, symptoms progress slowly, and the disease does not spread to normal bones. Treatment can control Paget's disease and lessen symptoms, but is not a cure. Osteogenic sarcoma, a form of bone cancer, is an extremely rare complication that occurs in less than one percent of all patients.

Associated medical conditions

Paget's disease may lead to other medical conditions, including:

• Arthritis may be caused by bowing of long bones in the leg, distorting alignment and increasing pressure on nearby joints. In addition, pagetic bone may enlarge, causing joint surfaces to undergo excessive wear. In these cases, pain may be due to a combination of Paget's disease and osteoarthritis.
• Loss of hearing in one or both ears may occur when Paget's disease affects the skull and the bone that surrounds the inner ear. Treating the Paget's disease may slow or stop hearing loss. Hearing aids may also help.
• Cardiovascular disease can result from severe Paget's disease (i.e. with more than 15% skeletal involvement). Arteriovenous connections can often form in the bone, and so the heart has to work harder (pump more blood) to ensure adequate oxygen supply to the tissues. This increase in cardiac output can lead to calcification of the aortic valve, and the resulting aortic stenosis causes left ventricular hypertrophy and eventually high-output congestive failure.
• Kidney stones are somewhat more common in patients with Paget's disease.
• Pagetic bone can cause nervous system problems, such as pressure on the brain, spinal cord, or nerves, and reduced blood flow to the brain and spinal cord.
• Rarely, Paget's disease is associated with the development of osteosarcoma (malignant tumor of bone). When there is a sudden onset or worsening of pain, sarcoma should be considered.
• When Paget's disease affects the facial bones, the teeth may become loose. Disturbance in chewing may occur.
• Rarely, when the skull is involved, the nerves to the eye may be affected, causing some loss of vision.
• Angioid streaks may develop, possibly as a result of calcification of collagen or other pathological deposition.

Paget's disease is not associated with osteoporosis. Although Paget's disease and osteoporosis can occur in the same patient, they are different disorders. Despite their marked differences, several treatments for Paget's disease are also used to treat osteoporosis.

Treatment

Endocrinologists (internists who specialize in hormonal and metabolic disorders), rheumatologists (internists who specialize in joint and muscle disorders), orthopedic surgeons, neurologists, oral and maxillofacial surgeons, podiatrists, and otolaryngologists are generally knowledgeable about treating Paget's disease, and may be called upon to evaluate specialized symptoms.

Drug therapy

The goal of treatment is to relieve bone pain and prevent the progression of the disease. The U.S. Food and Drug Administration has approved several treatments for Paget's disease.

Bisphosphonates

Five bisphosphonates are currently available. In general, the most commonly prescribed are risedronic acid (Actonel), alendronic acid (Fosamax), and pamidronic acid (Aredia). Etidronic acid (Didronel) and other bisphosphonates may be appropriate therapies for selected patients but are less commonly used. As a rule, bisphosphonate tablets should be taken with 200-250 mL (6–8& oz) of tap water (not from a source with high mineral content) on an empty stomach. None of these drugs should be used by people with severe kidney disease.

• Etidronate disodium (Didronel) in tablet form is available in 200–400 mg doses. The approved regimen is once daily for six months; the higher dose (400 mg) is more commonly used. No food, beverage, or medications should be consumed for two hours before and after taking. The course should not exceed six months, but repeat courses can be given after rest periods, preferably of three to six months duration.
• Pamidronate disodium (Aredia) in intravenous form: the approved regimen uses a 30 mg infusion over four hours on each of three consecutive days, but a more commonly used regimen is 60 mg over two to four hours for two or more consecutive or nonconsecutive days.
• Alendronate sodium (Fosamax) is given as tablets of 40 mg once daily for six months; patients should wait at least 30 minutes after taking before eating any food, drinking anything other than tap water, taking any medication, or lying down (patient may sit).
• Tiludronate disodium (Skelid) in two tablets of 200 mg are taken once daily for three months; they may be taken any time of day, as long as there is a period of two hours before and after resuming food, beverages, and medications.
• Risedronate sodium (Actonel) as a 30 mg tablet taken once daily for 2 months is the prescribed regimen; patients should wait at least 30 minutes after taking before eating any food, drinking anything other than tap water, taking any medication, or lying down (patient may sit).
• Zoledronic acid (Reclast, Aclasta) is given as an intravenous infusion; a single dose (5 mg over 15 minutes) is effective for two years.

Calcitonin

• Miacalcin is administered by injection; 50 to 100 units daily or three times per week for 6–18 months. Repeat courses can be given after brief rest periods. Miacalcin may be appropriate for certain patients, but is seldom used. The nasal spray form of this drug is not approved for the treatment of Paget's disease.

Surgery

Medical therapy prior to surgery helps to decrease bleeding and other complications. Patients who are having surgery should discuss treatment with their physician. There are generally three major complications of Paget's disease for which surgery may be recommended.

• Fractures — Surgery may allow fractures to heal in a better position.
• Severe degenerative arthritis — If disability is severe and medication and physical therapy are no longer helpful, joint replacement of the hips and knees may be considered.
• Bone deformity — Cutting and realignment of pagetic bone (osteotomy) may help painful weight bearing joints, especially the knees.

Complications resulting from enlargement of the skull or spine may injure the nervous system. However, most neurologic symptoms, even those that are moderately severe, can be treated with medication and do not require neurosurgery.

Diet and exercise

In general, patients with Paget's disease should receive 1000–1500 mg of calcium, adequate sunshine, and at least 400 units of vitamin D daily. This is especially important in patients being treated with bisphosphonates; however, taking oral bisphosphonates should be separated from taking calcium by at least two hours, because the calcium can inhibit the absorption of the bisphosphonate. Patients with a history of kidney stones should discuss calcium and vitamin D intake with their physicians.

Exercise is very important in maintaining skeletal health, avoiding weight gain, and maintaining joint mobility. Since undue stress on affected bones should be avoided, patients should discuss any exercise program with their physicians before beginning.

In culture

• C.S.I.: NY: A murder victim in Season 2 episode "Youngblood" was afflicted with Paget's disease.
• Retired Boston Red Sox center fielder Dom DiMaggio suffered from Paget's disease and served as a member of the board of directors of the Paget Foundation.
• Robot Chicken: Season 5: Kramer vs. Showgirls: The 90's Revisited: We learn that "Brain" of Pinky and the Brain was not a genius but his enlarged cranium is the result of Paget's disease, which has also left him blind.
• Egil, the main character in Egils Saga, may have suffered from this disease: he is described as being abnormally large and strong, and after death his skull was said to have been covered in ridges.
• Professor James Moriarty, a character in the Sherlock Holmes canon by Sir Srthur Conan Doyle, may have suffered from this disease. In The Final Problem (The Strand Magazine, Dec. 1893), he is described thus: "...his forehead domes out in a white curve", and that "...his face protrudes forward and is forever slowly oscillating from side to side in a curiously reptilian fashion". (Egil, above, is similarly described as having his head sway from side to side like a horse's, presumably from the extra weight of the bone.)
• The X-Files: Fox Mulder's mother commits suicide in Season 7, Episode 10 "Sein und Zeit", after being diagnosed with Paget's disease (called "Paget's Carcinoma" by Scully, but is likely Paget's Disease of Bone, not Paget's Disease of Breast, even though the latter is sometimes called "Paget's Carcinoma", since Scully describes the diseases highly disfiguring to explain the suicide).

References

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

• 1. 骨パジェット病の臨床症状および診断 clinical manifestations and diagnosis of paget disease of bone
• 2. 骨パジェット病の治療 treatment of paget disease of bone
• 3. 患者情報：骨パジェット病（変形性骨炎）（詳細） paget disease of bone osteitis deformans beyond the basics
• 4. 貨幣状頭痛 nummular headache
• 5. 高カルシウム血症の原因 etiology of hypercalcemia

English Journal

• Implications of a new radiological approach for the assessment of paget disease.

• Guañabens N, Rotés D, Holgado S, Gobbo M, Descalzo MA, Gorordo JM, Martínez-Ferrer MA, Salmoral A, Morales-Piga A.SourceDepartment of Rheumatology, Hospital Clínic, CIBERehd, C/Villarroel 170, 08036, Barcelona, Spain, nguanabens@ub.edu.
• Calcified tissue international.Calcif Tissue Int.2012 Dec;91(6):409-15. doi: 10.1007/s00223-012-9652-z. Epub 2012 Sep 30.
• In the present study, we quantified the proportion of skeletal involvement of Paget disease of bone (PDB) not captured by an abdominal X-ray. We also analyzed extension and severity over time and tested the hypothesis that X-rays from selected areas could replace bone scans for mapping PBD. We exami
• PMID 23052226

• SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

• Rubino E, Rainero I, Chiò A, Rogaeva E, Galimberti D, Fenoglio P, Grinberg Y, Isaia G, Calvo A, Gentile S, Bruni AC, St George-Hyslop PH, Scarpini E, Gallone S, Pinessi L; For the TODEM Study Group.SourceFrom Neurology II (E. Rubino, I.R., P.F., S. Gentile, S. Gallone, L.P.) and ALS Expert Center, Neurology IV (A. Chiò, A. Calvo), Department of Neuroscience, and Unit of Geriatrics and Metabolic Bone Disorders (G.I.), Department of Internal Medicine, University of Torino, Torino, Italy; Tanz Centre for Research in Neurodegenerative Diseases and Department of Medicine (E. Rogaeva, Y.G., P.H.St.G.-H.), University of Toronto, Toronto, Canada; Department of Neurological Sciences (D.G., E.S.), University of Milan, Centro Dino Ferrari, Fondazione Cà Granda IRCCS Ospedale Policlinico, Milan; Regional Neurogenetic Center (A.C.B.), ASP Catanzaro, Lamezia Terme, Italy; and Cambridge Institute for Medical Research and Department of Clinical Neurosciences (P.H.St.G.-H.), University of Cambridge, Cambridge, UK.
• Neurology.Neurology.2012 Oct 9;79(15):1556-1562. Epub 2012 Sep 12.
• OBJECTIVE: There is increasing evidence that common genetic risk factors underlie frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS). Recently, mutations in the sequestosome 1 (SQSTM1) gene, which encodes p62 protein, have been reported in patients with ALS. P62 is a mu
• PMID 22972638

Japanese Journal

• 大腿骨骨幹部骨折の治療に難渋した骨 Paget 病の1例

• 岸本 勇二,岡野 徹,豊島 良太
• 整形外科と災害外科 59(3), 606-609, 2010-09-25
• NAID 10026702018

Related Links

• Paget's disease of bone - Mayo Clinic

Paget's disease of bone — Comprehensive overview covers symptoms, causes, treatment of this chronic disorder. ... Paget's disease of bone disrupts your body's normal bone recycling process, in which old bone tissue is gradually ...

• Paget's Disease of Bone: MedlinePlus - National Library of ...

Paget's disease of bone causes your bones to grow too large and weak. They also might break easily. The disease can lead to other health problems, too, such as arthritis and hearing loss. You can have Paget's disease ...

Related Pictures

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★リンクテーブル★

リンク元	「骨パジェット病」
関連記事	「disease」「bone」

「骨パジェット病」

　　[★]

英

Paget's disease of bone、Paget disease of bone

同

変形性骨炎 osteitis deformans、骨ページェット病、骨Paget病

関

セメント線、パジェット病

「disease」

　　[★]

• n.

疾患：illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)

特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)

• something that is very wrong with people's attitudes, way of life or with society.

関

ail、ailment、disease entity、disorder、ill、illness、malady、sick、sickness

• 注意

disease ≠ illness ≠ disorder

　 　 　

「bone」

　　[★] 骨